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Published in: Clinical & Experimental Metastasis 6/2010

01-08-2010 | Research Paper

Functional genomics of endothelial cells treated with anti-angiogenic or angiopreventive drugs

Authors: Adriana Albini, Stefano Indraccolo, Douglas M. Noonan, Ulrich Pfeffer

Published in: Clinical & Experimental Metastasis | Issue 6/2010

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Abstract

Angiogenesis is a highly regulated physiological process that has been studied in considerable detail given its importance in several chronic pathologies. Many endogenous factors and hormones intervene in the regulation of angiogensis and classical as well as targeted drugs have been developed for its control. Angiogenesis inhibition has come off the bench and entered into clinical application for cancer therapy, particularly for metastatic disease. While the clinical benefit is currently in terms of months, preclinical data suggest that novel drugs and drug combinations could lead to substantial improvement. The many targets of endogenous angiogenesis inhibitors reflect the complexity of the process; in contrast, current clinical therapies mainly target the vascular endothelial growth factor system. Cancer chemopreventive compounds can retard tumor insurgence and delay or prevent metastasis and many of these molecules hinder angiogenesis, a mechanism that we termed angioprevention. Angiopreventive drugs appear to prevalently act through the inhibition of the pro-inflammatory and anti-apoptotic player NFκB, thus contrasting inflammation dependent angiogenesis. Relatively little is known concerning the effects of these angiogenesis inhibitors on gene expression of endothelial cells, the main target of many of these molecules. Here we provide an exhaustive list of anti-angiogenic molecules, and summarize their effects, where known, on the transcriptome and functional genomics of endothelial cells. The regulation of specific genes can be crucial to preventive or therapeutic intervention. Further, novel targets might help to circumvent resistance to anti-angiogenic therapy. The studies we review are relevant not only to cancer but also to other chronic degenerative diseases involving endothelial cells, such as cardiovascular disorders, diabetes, rheumatoid arthritis and retinopaties, as well as vessel aging.
Literature
1.
go back to reference Albini A, Sporn MB (2007) The tumour microenvironment as a target for chemoprevention. Nat Rev Cancer 7(2):139–147PubMedCrossRef Albini A, Sporn MB (2007) The tumour microenvironment as a target for chemoprevention. Nat Rev Cancer 7(2):139–147PubMedCrossRef
2.
go back to reference Casanovas O, Hicklin DJ, Bergers G et al (2005) Drug resistance by evasion of antiangiogenic targeting of VEGF signaling in late-stage pancreatic islet tumors. Cancer Cell 8(4):299–309PubMedCrossRef Casanovas O, Hicklin DJ, Bergers G et al (2005) Drug resistance by evasion of antiangiogenic targeting of VEGF signaling in late-stage pancreatic islet tumors. Cancer Cell 8(4):299–309PubMedCrossRef
3.
go back to reference Mizukami Y, Jo WS, Duerr EM et al (2005) Induction of interleukin-8 preserves the angiogenic response in HIF-1alpha-deficient colon cancer cells. Nat Med 11(9):992–997PubMed Mizukami Y, Jo WS, Duerr EM et al (2005) Induction of interleukin-8 preserves the angiogenic response in HIF-1alpha-deficient colon cancer cells. Nat Med 11(9):992–997PubMed
4.
go back to reference Rusnati M, Presta M (2007) Fibroblast growth factors/fibroblast growth factor receptors as targets for the development of anti-angiogenesis strategies. Curr Pharm Des 13(20):2025–2044PubMedCrossRef Rusnati M, Presta M (2007) Fibroblast growth factors/fibroblast growth factor receptors as targets for the development of anti-angiogenesis strategies. Curr Pharm Des 13(20):2025–2044PubMedCrossRef
5.
go back to reference Viloria-Petit A, Crombet T, Jothy S et al (2001) Acquired resistance to the antitumor effect of epidermal growth factor receptor-blocking antibodies in vivo: a role for altered tumor angiogenesis. Cancer Res 61(13):5090–5101PubMed Viloria-Petit A, Crombet T, Jothy S et al (2001) Acquired resistance to the antitumor effect of epidermal growth factor receptor-blocking antibodies in vivo: a role for altered tumor angiogenesis. Cancer Res 61(13):5090–5101PubMed
6.
go back to reference Albini A, Tosetti F, Benelli R et al (2005) Tumor inflammatory angiogenesis and its chemoprevention. Cancer Res 65(23):10637–10641PubMedCrossRef Albini A, Tosetti F, Benelli R et al (2005) Tumor inflammatory angiogenesis and its chemoprevention. Cancer Res 65(23):10637–10641PubMedCrossRef
7.
go back to reference Shojaei F, Wu X, Malik AK et al (2007) Tumor refractoriness to anti-VEGF treatment is mediated by CD11b+ Gr1 + myeloid cells. Nat Biotechnol 25(8):911–920PubMedCrossRef Shojaei F, Wu X, Malik AK et al (2007) Tumor refractoriness to anti-VEGF treatment is mediated by CD11b+ Gr1 + myeloid cells. Nat Biotechnol 25(8):911–920PubMedCrossRef
8.
go back to reference Shojaei F, Wu X, Zhong C et al (2007) Bv8 regulates myeloid-cell-dependent tumour angiogenesis. Nature 450(7171):825–831PubMedCrossRef Shojaei F, Wu X, Zhong C et al (2007) Bv8 regulates myeloid-cell-dependent tumour angiogenesis. Nature 450(7171):825–831PubMedCrossRef
9.
go back to reference Aplin AC, Gelati M, Fogel E et al (2006) Angiopoietin-1 and vascular endothelial growth factor induce expression of inflammatory cytokines before angiogenesis. Physiol Genomics 27(1):20–28PubMedCrossRef Aplin AC, Gelati M, Fogel E et al (2006) Angiopoietin-1 and vascular endothelial growth factor induce expression of inflammatory cytokines before angiogenesis. Physiol Genomics 27(1):20–28PubMedCrossRef
10.
go back to reference Sporn MB, Suh N (2002) Chemoprevention: an essential approach to controlling cancer. Nat Rev Cancer 2(7):537–543PubMedCrossRef Sporn MB, Suh N (2002) Chemoprevention: an essential approach to controlling cancer. Nat Rev Cancer 2(7):537–543PubMedCrossRef
11.
go back to reference Tosetti F, Ferrari N, De Flora S et al (2002) Angioprevention’: angiogenesis is a common and key target for cancer chemopreventive agents. FASEB J 16(1):2–14PubMedCrossRef Tosetti F, Ferrari N, De Flora S et al (2002) Angioprevention’: angiogenesis is a common and key target for cancer chemopreventive agents. FASEB J 16(1):2–14PubMedCrossRef
12.
go back to reference Sudhakar A, Nyberg P, Keshamouni VG et al (2005) Human alpha1 type IV collagen NC1 domain exhibits distinct antiangiogenic activity mediated by alpha1beta1 integrin. J Clin Invest 115(10):2801–2810PubMedCrossRef Sudhakar A, Nyberg P, Keshamouni VG et al (2005) Human alpha1 type IV collagen NC1 domain exhibits distinct antiangiogenic activity mediated by alpha1beta1 integrin. J Clin Invest 115(10):2801–2810PubMedCrossRef
13.
go back to reference Kamphaus GD, Colorado PC, Panka DJ et al (2000) Canstatin, a novel matrix-derived inhibitor of angiogenesis and tumor growth. J Biol Chem 275(2):1209–1215PubMedCrossRef Kamphaus GD, Colorado PC, Panka DJ et al (2000) Canstatin, a novel matrix-derived inhibitor of angiogenesis and tumor growth. J Biol Chem 275(2):1209–1215PubMedCrossRef
14.
go back to reference Petitclerc E, Boutaud A, Prestayko A et al (2000) New functions for non-collagenous domains of human collagen type IV. Novel integrin ligands inhibiting angiogenesis and tumor growth in vivo. J Biol Chem 275(11):8051–8061PubMedCrossRef Petitclerc E, Boutaud A, Prestayko A et al (2000) New functions for non-collagenous domains of human collagen type IV. Novel integrin ligands inhibiting angiogenesis and tumor growth in vivo. J Biol Chem 275(11):8051–8061PubMedCrossRef
15.
go back to reference Maeshima Y, Yerramalla UL, Dhanabal M et al (2001) Extracellular matrix-derived peptide binds to alpha(v)beta(3) integrin and inhibits angiogenesis. J Biol Chem 276(34):31959–31968PubMedCrossRef Maeshima Y, Yerramalla UL, Dhanabal M et al (2001) Extracellular matrix-derived peptide binds to alpha(v)beta(3) integrin and inhibits angiogenesis. J Biol Chem 276(34):31959–31968PubMedCrossRef
16.
go back to reference O’Reilly MS, Boehm T, Shing Y et al (1997) Endostatin: an endogenous inhibitor of angiogenesis and tumor growth. Cell 88(2):277–285PubMedCrossRef O’Reilly MS, Boehm T, Shing Y et al (1997) Endostatin: an endogenous inhibitor of angiogenesis and tumor growth. Cell 88(2):277–285PubMedCrossRef
17.
go back to reference Mongiat M, Sweeney SM, San Antonio JD et al (2003) Endorepellin, a novel inhibitor of angiogenesis derived from the C terminus of perlecan. J Biol Chem 278(6):4238–4249PubMedCrossRef Mongiat M, Sweeney SM, San Antonio JD et al (2003) Endorepellin, a novel inhibitor of angiogenesis derived from the C terminus of perlecan. J Biol Chem 278(6):4238–4249PubMedCrossRef
18.
go back to reference Yi M, Ruoslahti E (2001) A fibronectin fragment inhibits tumor growth, angiogenesis, and metastasis. Proc Natl Acad Sci USA 98(2):620–624PubMedCrossRef Yi M, Ruoslahti E (2001) A fibronectin fragment inhibits tumor growth, angiogenesis, and metastasis. Proc Natl Acad Sci USA 98(2):620–624PubMedCrossRef
19.
go back to reference Good DJ, Polverini PJ, Rastinejad F et al (1990) A tumor suppressor-dependent inhibitor of angiogenesis is immunologically and functionally indistinguishable from a fragment of thrombospondin. Proc Natl Acad Sci USA 87(17):6624–6628PubMedCrossRef Good DJ, Polverini PJ, Rastinejad F et al (1990) A tumor suppressor-dependent inhibitor of angiogenesis is immunologically and functionally indistinguishable from a fragment of thrombospondin. Proc Natl Acad Sci USA 87(17):6624–6628PubMedCrossRef
20.
go back to reference Taraboletti G, Roberts D, Liotta LA et al (1990) Platelet thrombospondin modulates endothelial cell adhesion, motility, and growth: a potential angiogenesis regulatory factor. J Cell Biol 111(2):765–772PubMedCrossRef Taraboletti G, Roberts D, Liotta LA et al (1990) Platelet thrombospondin modulates endothelial cell adhesion, motility, and growth: a potential angiogenesis regulatory factor. J Cell Biol 111(2):765–772PubMedCrossRef
21.
go back to reference Garlanda C, Bottazzi B, Bastone A et al (2005) Pentraxins at the crossroads between innate immunity, inflammation, matrix deposition, and female fertility. Annu Rev Immunol 23:337–366PubMedCrossRef Garlanda C, Bottazzi B, Bastone A et al (2005) Pentraxins at the crossroads between innate immunity, inflammation, matrix deposition, and female fertility. Annu Rev Immunol 23:337–366PubMedCrossRef
22.
go back to reference Margheri F, Serrati S, Lapucci A et al (2009) Systemic sclerosis-endothelial cell antiangiogenic pentraxin 3 and matrix metalloprotease 12 control human breast cancer tumor vascularization and development in mice. Neoplasia 11(10):1106–1115PubMed Margheri F, Serrati S, Lapucci A et al (2009) Systemic sclerosis-endothelial cell antiangiogenic pentraxin 3 and matrix metalloprotease 12 control human breast cancer tumor vascularization and development in mice. Neoplasia 11(10):1106–1115PubMed
23.
go back to reference Alessi P, Leali D, Camozzi M et al (2009) Anti-FGF2 approaches as a strategy to compensate resistance to anti-VEGF therapy: long-pentraxin 3 as a novel antiangiogenic FGF2-antagonist. Eur Cytokine Netw 20(4):225–234PubMed Alessi P, Leali D, Camozzi M et al (2009) Anti-FGF2 approaches as a strategy to compensate resistance to anti-VEGF therapy: long-pentraxin 3 as a novel antiangiogenic FGF2-antagonist. Eur Cytokine Netw 20(4):225–234PubMed
24.
go back to reference Moses MA, Sudhalter J, Langer R (1990) Identification of an inhibitor of neovascularization from cartilage. Science 248(4961):1408–1410PubMedCrossRef Moses MA, Sudhalter J, Langer R (1990) Identification of an inhibitor of neovascularization from cartilage. Science 248(4961):1408–1410PubMedCrossRef
25.
go back to reference Rastinejad F, Polverini PJ, Bouck NP (1989) Regulation of the activity of a new inhibitor of angiogenesis by a cancer suppressor gene. Cell 56(3):345–355PubMedCrossRef Rastinejad F, Polverini PJ, Bouck NP (1989) Regulation of the activity of a new inhibitor of angiogenesis by a cancer suppressor gene. Cell 56(3):345–355PubMedCrossRef
26.
go back to reference O’Reilly MS, Pirie-Shepherd S, Lane WS et al (1999) Antiangiogenic activity of the cleaved conformation of the serpin antithrombin. Science 285(5435):1926–1928PubMedCrossRef O’Reilly MS, Pirie-Shepherd S, Lane WS et al (1999) Antiangiogenic activity of the cleaved conformation of the serpin antithrombin. Science 285(5435):1926–1928PubMedCrossRef
27.
go back to reference Pike SE, Yao L, Jones KD et al (1998) Vasostatin, a calreticulin fragment, inhibits angiogenesis and suppresses tumor growth. J Exp Med 188(12):2349–2356PubMedCrossRef Pike SE, Yao L, Jones KD et al (1998) Vasostatin, a calreticulin fragment, inhibits angiogenesis and suppresses tumor growth. J Exp Med 188(12):2349–2356PubMedCrossRef
28.
go back to reference Okamura Y, Watari M, Jerud ES et al (2001) The extra domain A of fibronectin activates Toll-like receptor 4. J Biol Chem 276(13):10229–10233PubMedCrossRef Okamura Y, Watari M, Jerud ES et al (2001) The extra domain A of fibronectin activates Toll-like receptor 4. J Biol Chem 276(13):10229–10233PubMedCrossRef
29.
go back to reference Huegel R, Velasco P, De La Luz Sierra M et al (2007) Novel anti-inflammatory properties of the angiogenesis inhibitor vasostatin. J Invest Dermatol 127(1):65–74PubMedCrossRef Huegel R, Velasco P, De La Luz Sierra M et al (2007) Novel anti-inflammatory properties of the angiogenesis inhibitor vasostatin. J Invest Dermatol 127(1):65–74PubMedCrossRef
30.
31.
go back to reference Maione TE, Gray GS, Petro J et al (1990) Inhibition of angiogenesis by recombinant human platelet factor-4 and related peptides. Science 247(4938):77–79PubMedCrossRef Maione TE, Gray GS, Petro J et al (1990) Inhibition of angiogenesis by recombinant human platelet factor-4 and related peptides. Science 247(4938):77–79PubMedCrossRef
32.
go back to reference Sharpe RJ, Byers HR, Scott CF et al (1990) Growth inhibition of murine melanoma and human colon carcinoma by recombinant human platelet factor 4. J Natl Cancer Inst 82(10):848–853PubMedCrossRef Sharpe RJ, Byers HR, Scott CF et al (1990) Growth inhibition of murine melanoma and human colon carcinoma by recombinant human platelet factor 4. J Natl Cancer Inst 82(10):848–853PubMedCrossRef
33.
go back to reference Kendall RL, Thomas KA (1993) Inhibition of vascular endothelial cell growth factor activity by an endogenously encoded soluble receptor. Proc Natl Acad Sci USA 90(22):10705–10709PubMedCrossRef Kendall RL, Thomas KA (1993) Inhibition of vascular endothelial cell growth factor activity by an endogenously encoded soluble receptor. Proc Natl Acad Sci USA 90(22):10705–10709PubMedCrossRef
34.
go back to reference Dawson DW, Volpert OV, Gillis P et al (1999) Pigment epithelium-derived factor: a potent inhibitor of angiogenesis. Science 285(5425):245–248PubMedCrossRef Dawson DW, Volpert OV, Gillis P et al (1999) Pigment epithelium-derived factor: a potent inhibitor of angiogenesis. Science 285(5425):245–248PubMedCrossRef
35.
go back to reference Maisonpierre PC, Suri C, Jones PF et al (1997) Angiopoietin-2, a natural antagonist for Tie2 that disrupts in vivo angiogenesis. Science 277(5322):55–60PubMedCrossRef Maisonpierre PC, Suri C, Jones PF et al (1997) Angiopoietin-2, a natural antagonist for Tie2 that disrupts in vivo angiogenesis. Science 277(5322):55–60PubMedCrossRef
36.
go back to reference Bates DO, Cui TG, Doughty JM et al (2002) VEGF165b, an inhibitory splice variant of vascular endothelial growth factor, is down-regulated in renal cell carcinoma. Cancer Res 62(14):4123–4131PubMed Bates DO, Cui TG, Doughty JM et al (2002) VEGF165b, an inhibitory splice variant of vascular endothelial growth factor, is down-regulated in renal cell carcinoma. Cancer Res 62(14):4123–4131PubMed
37.
go back to reference O’Reilly MS, Holmgren L, Shing Y et al (1994) Angiostatin: a novel angiogenesis inhibitor that mediates the suppression of metastases by a Lewis lung carcinoma. Cell 79(2):315–328PubMedCrossRef O’Reilly MS, Holmgren L, Shing Y et al (1994) Angiostatin: a novel angiogenesis inhibitor that mediates the suppression of metastases by a Lewis lung carcinoma. Cell 79(2):315–328PubMedCrossRef
38.
go back to reference Abad M, Arni R, Grella D et al (2002) The X-ray crystallographic structure of the angiogenesis inhibitor angiostatin. J Mol Biol 318:1009–1017PubMedCrossRef Abad M, Arni R, Grella D et al (2002) The X-ray crystallographic structure of the angiogenesis inhibitor angiostatin. J Mol Biol 318:1009–1017PubMedCrossRef
39.
go back to reference O’Reilly MS, Wiederschain D, Stetler SW et al (1999) Regulation of angiostatin production by matrix metalloproteinase-2 in a model of concomitant resistance. J Biol Chem 274(41):29568–29571PubMedCrossRef O’Reilly MS, Wiederschain D, Stetler SW et al (1999) Regulation of angiostatin production by matrix metalloproteinase-2 in a model of concomitant resistance. J Biol Chem 274(41):29568–29571PubMedCrossRef
40.
go back to reference Paleari L, Brigati C, Anfosso L et al (2005) Anti-angiogenesis in search of mechanisms: angiostatin as a prototype. In: Weber GF (ed) Cancer therapy: molecular targets in tumor-host interactions. Horizon Scientific Press, Norfolk, pp 143–168 Paleari L, Brigati C, Anfosso L et al (2005) Anti-angiogenesis in search of mechanisms: angiostatin as a prototype. In: Weber GF (ed) Cancer therapy: molecular targets in tumor-host interactions. Horizon Scientific Press, Norfolk, pp 143–168
41.
go back to reference Ito H, Rovira II, Bloom ML et al (1999) Endothelial progenitor cells as putative targets for angiostatin. Cancer Res 59(23):5875–5877PubMed Ito H, Rovira II, Bloom ML et al (1999) Endothelial progenitor cells as putative targets for angiostatin. Cancer Res 59(23):5875–5877PubMed
42.
go back to reference Walter JJ, Sane DC (1999) Angiostatin binds to smooth muscle cells in the coronary artery and inhibits smooth muscle cell proliferation and migration In vitro. Arterioscler Thromb Vasc Biol 19(9):2041–2048PubMed Walter JJ, Sane DC (1999) Angiostatin binds to smooth muscle cells in the coronary artery and inhibits smooth muscle cell proliferation and migration In vitro. Arterioscler Thromb Vasc Biol 19(9):2041–2048PubMed
43.
go back to reference Moser T, Kenan D, Ashley T et al (2001) Endothelial cell surface F1–F0 ATP synthase is active in ATP synthesis and is inhibited by angiostatin. Proc Natl Acad Sci USA 98:6656–6661PubMedCrossRef Moser T, Kenan D, Ashley T et al (2001) Endothelial cell surface F1–F0 ATP synthase is active in ATP synthesis and is inhibited by angiostatin. Proc Natl Acad Sci USA 98:6656–6661PubMedCrossRef
44.
go back to reference Benelli R, Morini M, Carrozzino F et al (2002) Neutrophils as a key cellular target for angiostatin: implications for regulation of angiogenesis and inflammation. FASEB J 16:267–269PubMed Benelli R, Morini M, Carrozzino F et al (2002) Neutrophils as a key cellular target for angiostatin: implications for regulation of angiogenesis and inflammation. FASEB J 16:267–269PubMed
45.
go back to reference Wahl ML, Kenan DJ, Gonzalez-Gronow M et al (2005) Angiostatin’s molecular mechanism: aspects of specificity and regulation elucidated. J Cell Biochem 96(2):242–261PubMedCrossRef Wahl ML, Kenan DJ, Gonzalez-Gronow M et al (2005) Angiostatin’s molecular mechanism: aspects of specificity and regulation elucidated. J Cell Biochem 96(2):242–261PubMedCrossRef
46.
go back to reference Chavakis T, Athanasopoulos A, Rhee JS et al (2005) Angiostatin is a novel anti-inflammatory factor by inhibiting leukocyte recruitment. Blood 105(3):1036–1043PubMedCrossRef Chavakis T, Athanasopoulos A, Rhee JS et al (2005) Angiostatin is a novel anti-inflammatory factor by inhibiting leukocyte recruitment. Blood 105(3):1036–1043PubMedCrossRef
47.
go back to reference Benelli R, Morini M, Brigati C et al (2003) Angiostatin inhibits extracellular HIV-Tat-induced inflammatory angiogenesis. Int J Oncol 22(1):87–91PubMed Benelli R, Morini M, Brigati C et al (2003) Angiostatin inhibits extracellular HIV-Tat-induced inflammatory angiogenesis. Int J Oncol 22(1):87–91PubMed
48.
go back to reference Moulton KS, Vakili K, Zurakowski D et al (2003) Inhibition of plaque neovascularization reduces macrophage accumulation and progression of advanced atherosclerosis. Proc Natl Acad Sci USA 100(8):4736–4741PubMedCrossRef Moulton KS, Vakili K, Zurakowski D et al (2003) Inhibition of plaque neovascularization reduces macrophage accumulation and progression of advanced atherosclerosis. Proc Natl Acad Sci USA 100(8):4736–4741PubMedCrossRef
49.
go back to reference Perri SR, Nalbantoglu J, Annabi B et al (2005) Plasminogen kringle 5-engineered glioma cells block migration of tumor-associated macrophages and suppress tumor vascularization and progression. Cancer Res 65(18):8359–8365PubMedCrossRef Perri SR, Nalbantoglu J, Annabi B et al (2005) Plasminogen kringle 5-engineered glioma cells block migration of tumor-associated macrophages and suppress tumor vascularization and progression. Cancer Res 65(18):8359–8365PubMedCrossRef
50.
go back to reference Indraccolo S, Pfeffer U, Minuzzo S et al (2007) Identification of genes selectively regulated by interferons in endothelial cells. J Immunol 178(2):1122–1135PubMed Indraccolo S, Pfeffer U, Minuzzo S et al (2007) Identification of genes selectively regulated by interferons in endothelial cells. J Immunol 178(2):1122–1135PubMed
51.
go back to reference Torpey N, Maher SE, Bothwell AL et al (2004) Interferon alpha but not interleukin 12 activates STAT4 signaling in human vascular endothelial cells. J Biol Chem 279(25):26789–26796PubMedCrossRef Torpey N, Maher SE, Bothwell AL et al (2004) Interferon alpha but not interleukin 12 activates STAT4 signaling in human vascular endothelial cells. J Biol Chem 279(25):26789–26796PubMedCrossRef
52.
go back to reference Albini A, Brigati C, Ventura A et al (2009) Angiostatin anti-angiogenesis requires IL-12: the innate immune system as a key target. J Transl Med 7:5PubMedCrossRef Albini A, Brigati C, Ventura A et al (2009) Angiostatin anti-angiogenesis requires IL-12: the innate immune system as a key target. J Transl Med 7:5PubMedCrossRef
53.
go back to reference Morini M, Albini A, Lorusso G et al (2004) Prevention of angiogenesis by naked DNA IL-12 gene transfer: angioprevention by immunogene therapy. Gene Ther 11(3):284–291PubMedCrossRef Morini M, Albini A, Lorusso G et al (2004) Prevention of angiogenesis by naked DNA IL-12 gene transfer: angioprevention by immunogene therapy. Gene Ther 11(3):284–291PubMedCrossRef
54.
go back to reference Chen YH, Wu HL, Li C et al. (2006) Anti-angiogenesis mediated by angiostatin K1-3, K1-4 and K1-4.5. Involvement of p53, FasL, AKT and mRNA deregulation. Thromb Haemost 95(4):668–677 Chen YH, Wu HL, Li C et al. (2006) Anti-angiogenesis mediated by angiostatin K1-3, K1-4 and K1-4.5. Involvement of p53, FasL, AKT and mRNA deregulation. Thromb Haemost 95(4):668–677
55.
go back to reference Yu Y, Moulton KS, Khan MK et al (2004) E-selectin is required for the antiangiogenic activity of endostatin. Proc Natl Acad Sci USA 101(21):8005–8010PubMedCrossRef Yu Y, Moulton KS, Khan MK et al (2004) E-selectin is required for the antiangiogenic activity of endostatin. Proc Natl Acad Sci USA 101(21):8005–8010PubMedCrossRef
56.
go back to reference Vannini N, Pfeffer U, Lorusso G et al (2008) Endothelial cell aging and apoptosis in prevention and disease: E-selectin expression and modulation as a model. Curr Pharm Des 14(3):221–225PubMedCrossRef Vannini N, Pfeffer U, Lorusso G et al (2008) Endothelial cell aging and apoptosis in prevention and disease: E-selectin expression and modulation as a model. Curr Pharm Des 14(3):221–225PubMedCrossRef
57.
go back to reference Mazzanti CM, Tandle A, Lorang D et al (2004) Early genetic mechanisms underlying the inhibitory effects of endostatin and fumagillin on human endothelial cells. Genome Res 14(8):1585–1593PubMedCrossRef Mazzanti CM, Tandle A, Lorang D et al (2004) Early genetic mechanisms underlying the inhibitory effects of endostatin and fumagillin on human endothelial cells. Genome Res 14(8):1585–1593PubMedCrossRef
58.
go back to reference Hanai J, Gloy J, Karumanchi SA et al (2002) Endostatin is a potential inhibitor of Wnt signaling. J Cell Biol 158(3):529–539PubMedCrossRef Hanai J, Gloy J, Karumanchi SA et al (2002) Endostatin is a potential inhibitor of Wnt signaling. J Cell Biol 158(3):529–539PubMedCrossRef
59.
go back to reference Schmidt A, Wenzel D, Thorey I et al (2006) Endostatin influences endothelial morphology via the activated ERK1/2-kinase endothelial morphology and signal transduction. Microvasc Res 71(3):152–162PubMedCrossRef Schmidt A, Wenzel D, Thorey I et al (2006) Endostatin influences endothelial morphology via the activated ERK1/2-kinase endothelial morphology and signal transduction. Microvasc Res 71(3):152–162PubMedCrossRef
60.
go back to reference Wickstrom SA, Alitalo K, Keski-Oja J (2002) Endostatin associates with integrin alpha5beta1 and caveolin-1, and activates Src via a tyrosyl phosphatase-dependent pathway in human endothelial cells. Cancer Res 62(19):5580–5589PubMed Wickstrom SA, Alitalo K, Keski-Oja J (2002) Endostatin associates with integrin alpha5beta1 and caveolin-1, and activates Src via a tyrosyl phosphatase-dependent pathway in human endothelial cells. Cancer Res 62(19):5580–5589PubMed
61.
go back to reference Zhang W, Chuang YJ, Swanson R et al (2004) Antiangiogenic antithrombin down-regulates the expression of the proangiogenic heparan sulfate proteoglycan, perlecan, in endothelial cells. Blood 103(4):1185–1191PubMedCrossRef Zhang W, Chuang YJ, Swanson R et al (2004) Antiangiogenic antithrombin down-regulates the expression of the proangiogenic heparan sulfate proteoglycan, perlecan, in endothelial cells. Blood 103(4):1185–1191PubMedCrossRef
62.
go back to reference Noonan DM, Fulle A, Valente P et al (1991) The complete sequence of perlecan, a basement membrane heparan sulfate proteoglycan, reveals extensive similarity with laminin A chain, low density lipoprotein-receptor, and the neural cell adhesion molecule. J Biol Chem 266(34):22939–22947PubMed Noonan DM, Fulle A, Valente P et al (1991) The complete sequence of perlecan, a basement membrane heparan sulfate proteoglycan, reveals extensive similarity with laminin A chain, low density lipoprotein-receptor, and the neural cell adhesion molecule. J Biol Chem 266(34):22939–22947PubMed
63.
go back to reference Aviezer D, Iozzo RV, Noonan DM et al (1997) Suppression of autocrine and paracrine functions of basic fibroblast growth factor by stable expression of perlecan antisense cDNA. Mol Cell Biol 17(4):1938–1946PubMed Aviezer D, Iozzo RV, Noonan DM et al (1997) Suppression of autocrine and paracrine functions of basic fibroblast growth factor by stable expression of perlecan antisense cDNA. Mol Cell Biol 17(4):1938–1946PubMed
64.
go back to reference Zhang W, Chuang YJ, Jin T et al (2006) Antiangiogenic antithrombin induces global changes in the gene expression profile of endothelial cells. Cancer Res 66(10):5047–5055PubMedCrossRef Zhang W, Chuang YJ, Jin T et al (2006) Antiangiogenic antithrombin induces global changes in the gene expression profile of endothelial cells. Cancer Res 66(10):5047–5055PubMedCrossRef
65.
go back to reference Guedez L, Martinez A, Zhao S et al (2005) Tissue inhibitor of metalloproteinase 1 (TIMP-1) promotes plasmablastic differentiation of a Burkitt lymphoma cell line: implications in the pathogenesis of plasmacytic/plasmablastic tumors. Blood 105(4):1660–1668PubMedCrossRef Guedez L, Martinez A, Zhao S et al (2005) Tissue inhibitor of metalloproteinase 1 (TIMP-1) promotes plasmablastic differentiation of a Burkitt lymphoma cell line: implications in the pathogenesis of plasmacytic/plasmablastic tumors. Blood 105(4):1660–1668PubMedCrossRef
66.
go back to reference Lam P, Sian Lim K, Mei Wang S et al (2005) A microarray study to characterize the molecular mechanism of TIMP-3-mediated tumor rejection. Mol Ther 12(1):144–152PubMedCrossRef Lam P, Sian Lim K, Mei Wang S et al (2005) A microarray study to characterize the molecular mechanism of TIMP-3-mediated tumor rejection. Mol Ther 12(1):144–152PubMedCrossRef
67.
go back to reference Fotsis T, Zhang Y, Pepper MS et al (1994) The endogenous oestrogen metabolite 2-methoxyoestradiol inhibits angiogenesis and suppresses tumour growth. Nature 368(6468):237–239PubMedCrossRef Fotsis T, Zhang Y, Pepper MS et al (1994) The endogenous oestrogen metabolite 2-methoxyoestradiol inhibits angiogenesis and suppresses tumour growth. Nature 368(6468):237–239PubMedCrossRef
68.
go back to reference Wood L, Leese MR, Leblond B et al (2001) Inhibition of superoxide dismutase by 2-methoxyoestradiol analogues and oestrogen derivatives: structure-activity relationships. Anticancer Drug Des 16(4–5):209–215PubMed Wood L, Leese MR, Leblond B et al (2001) Inhibition of superoxide dismutase by 2-methoxyoestradiol analogues and oestrogen derivatives: structure-activity relationships. Anticancer Drug Des 16(4–5):209–215PubMed
69.
go back to reference Albini A, Paglieri I, Orengo G et al (1997) The beta-core fragment of human chorionic gonadotrophin inhibits growth of Kaposi’s sarcoma-derived cells and a new immortalized Kaposi’s sarcoma cell line. AIDS 11(6):713–721PubMedCrossRef Albini A, Paglieri I, Orengo G et al (1997) The beta-core fragment of human chorionic gonadotrophin inhibits growth of Kaposi’s sarcoma-derived cells and a new immortalized Kaposi’s sarcoma cell line. AIDS 11(6):713–721PubMedCrossRef
70.
go back to reference Pfeffer U, Bisacchi D, Morini M et al (2002) Human chorionic gonadotropin inhibits Kaposi’s sarcoma associated angiogenesis, matrix metalloprotease activity, and tumor growth. Endocrinology 143(8):3114–3121PubMedCrossRef Pfeffer U, Bisacchi D, Morini M et al (2002) Human chorionic gonadotropin inhibits Kaposi’s sarcoma associated angiogenesis, matrix metalloprotease activity, and tumor growth. Endocrinology 143(8):3114–3121PubMedCrossRef
71.
go back to reference Guo S, Russo IH, Lareef MH et al (2004) Effect of human chorionic gonadotropin in the gene expression profile of MCF-7 cells. Int J Oncol 24(2):399–407PubMed Guo S, Russo IH, Lareef MH et al (2004) Effect of human chorionic gonadotropin in the gene expression profile of MCF-7 cells. Int J Oncol 24(2):399–407PubMed
72.
go back to reference Florio T, Morini M, Villa V et al (2003) Somatostatin inhibits tumor angiogenesis and growth via somatostatin receptor-3-mediated regulation of endothelial nitric oxide synthase and mitogen-activated protein kinase activities. Endocrinology 144(4):1574–1584PubMedCrossRef Florio T, Morini M, Villa V et al (2003) Somatostatin inhibits tumor angiogenesis and growth via somatostatin receptor-3-mediated regulation of endothelial nitric oxide synthase and mitogen-activated protein kinase activities. Endocrinology 144(4):1574–1584PubMedCrossRef
73.
go back to reference Patel SG, Zhou G, Liu SH et al (2009) Microarray analysis of somatostatin receptor 5-regulated gene expression profiles in murine pancreas. World J Surg 33(4):630–637PubMedCrossRef Patel SG, Zhou G, Liu SH et al (2009) Microarray analysis of somatostatin receptor 5-regulated gene expression profiles in murine pancreas. World J Surg 33(4):630–637PubMedCrossRef
74.
go back to reference D’Angelo G, Struman I, Martial J et al (1995) Activation of mitogen-activated protein kinases by vascular endothelial growth factor and basic fibroblast growth factor in capillary endothelial cells is inhibited by the antiangiogenic factor 16-kDa N-terminal fragment of prolactin. Proc Natl Acad Sci USA 92(14):6374–6378PubMedCrossRef D’Angelo G, Struman I, Martial J et al (1995) Activation of mitogen-activated protein kinases by vascular endothelial growth factor and basic fibroblast growth factor in capillary endothelial cells is inhibited by the antiangiogenic factor 16-kDa N-terminal fragment of prolactin. Proc Natl Acad Sci USA 92(14):6374–6378PubMedCrossRef
75.
go back to reference Struman I, Bentzien F, Lee H et al (1999) Opposing actions of intact and N-terminal fragments of the human prolactin/growth hormone family members on angiogenesis: an efficient mechanism for the regulation of angiogenesis. Proc Natl Acad Sci USA 96(4):1246–1251PubMedCrossRef Struman I, Bentzien F, Lee H et al (1999) Opposing actions of intact and N-terminal fragments of the human prolactin/growth hormone family members on angiogenesis: an efficient mechanism for the regulation of angiogenesis. Proc Natl Acad Sci USA 96(4):1246–1251PubMedCrossRef
76.
go back to reference Tabruyn SP, Sabatel C, Nguyen NQ et al (2007) The angiostatic 16 K human prolactin overcomes endothelial cell anergy and promotes leukocyte infiltration via nuclear factor-kappaB activation. Mol Endocrinol 21(6):1422–1429PubMedCrossRef Tabruyn SP, Sabatel C, Nguyen NQ et al (2007) The angiostatic 16 K human prolactin overcomes endothelial cell anergy and promotes leukocyte infiltration via nuclear factor-kappaB activation. Mol Endocrinol 21(6):1422–1429PubMedCrossRef
77.
go back to reference Pfeffer U, Ferrari N, Dell’Eva R et al (2005) Molecular mechanisms of action of angiopreventive anti-oxidants on endothelial cells: microarray gene expression analyses. Mutat Res 591(1–2):198–211PubMed Pfeffer U, Ferrari N, Dell’Eva R et al (2005) Molecular mechanisms of action of angiopreventive anti-oxidants on endothelial cells: microarray gene expression analyses. Mutat Res 591(1–2):198–211PubMed
78.
go back to reference Kanda N, Watanabe S (2007) Prolactin enhances interferon-gamma-induced production of CXC ligand 9 (CXCL9), CXCL10, and CXCL11 in human keratinocytes. Endocrinology 148(5):2317–2325PubMedCrossRef Kanda N, Watanabe S (2007) Prolactin enhances interferon-gamma-induced production of CXC ligand 9 (CXCL9), CXCL10, and CXCL11 in human keratinocytes. Endocrinology 148(5):2317–2325PubMedCrossRef
79.
go back to reference Dvorak HF, Gresser I (1989) Microvascular injury in pathogenesis of interferon-induced necrosis of subcutaneous tumors in mice. J Natl Cancer Inst 81(7):497–502PubMedCrossRef Dvorak HF, Gresser I (1989) Microvascular injury in pathogenesis of interferon-induced necrosis of subcutaneous tumors in mice. J Natl Cancer Inst 81(7):497–502PubMedCrossRef
80.
go back to reference Sidky YA, Borden EC (1987) Inhibition of angiogenesis by interferons: effects on tumor- and lymphocyte-induced vascular responses. Cancer Res 47(19):5155–5161PubMed Sidky YA, Borden EC (1987) Inhibition of angiogenesis by interferons: effects on tumor- and lymphocyte-induced vascular responses. Cancer Res 47(19):5155–5161PubMed
81.
go back to reference Minuzzo S, Moserle L, Indraccolo S et al (2007) Angiogenesis meets immunology: cytokine gene therapy of cancer. Mol Aspects Med 28(1):59–86PubMedCrossRef Minuzzo S, Moserle L, Indraccolo S et al (2007) Angiogenesis meets immunology: cytokine gene therapy of cancer. Mol Aspects Med 28(1):59–86PubMedCrossRef
82.
go back to reference Singh RP, Dhanalakshmi S, Agarwal C et al (2005) Silibinin strongly inhibits growth and survival of human endothelial cells via cell cycle arrest and downregulation of survivin, Akt and NF-kappaB: implications for angioprevention and antiangiogenic therapy. Oncogene 24(7):1188–1202PubMedCrossRef Singh RP, Dhanalakshmi S, Agarwal C et al (2005) Silibinin strongly inhibits growth and survival of human endothelial cells via cell cycle arrest and downregulation of survivin, Akt and NF-kappaB: implications for angioprevention and antiangiogenic therapy. Oncogene 24(7):1188–1202PubMedCrossRef
83.
go back to reference Oliveira IC, Sciavolino PJ, Lee TH et al (1992) Downregulation of interleukin 8 gene expression in human fibroblasts: unique mechanism of transcriptional inhibition by interferon. Proc Natl Acad Sci USA 89(19):9049–9053PubMedCrossRef Oliveira IC, Sciavolino PJ, Lee TH et al (1992) Downregulation of interleukin 8 gene expression in human fibroblasts: unique mechanism of transcriptional inhibition by interferon. Proc Natl Acad Sci USA 89(19):9049–9053PubMedCrossRef
84.
go back to reference von Marschall Z, Scholz A, Cramer T et al (2003) Effects of interferon alpha on vascular endothelial growth factor gene transcription and tumor angiogenesis. J Natl Cancer Inst 95(6):437–448CrossRef von Marschall Z, Scholz A, Cramer T et al (2003) Effects of interferon alpha on vascular endothelial growth factor gene transcription and tumor angiogenesis. J Natl Cancer Inst 95(6):437–448CrossRef
85.
go back to reference Albini A, Marchisone C, Del Grosso F et al (2000) Inhibition of angiogenesis and vascular tumor growth by interferon-producing cells: A gene therapy approach. Am J Pathol 156(4):1381–1393PubMed Albini A, Marchisone C, Del Grosso F et al (2000) Inhibition of angiogenesis and vascular tumor growth by interferon-producing cells: A gene therapy approach. Am J Pathol 156(4):1381–1393PubMed
86.
go back to reference Indraccolo S, Gola E, Rosato A et al (2002) Differential effects of angiostatin, endostatin and interferon-alpha(1) gene transfer on in vivo growth of human breast cancer cells. Gene Ther 9(13):867–878PubMedCrossRef Indraccolo S, Gola E, Rosato A et al (2002) Differential effects of angiostatin, endostatin and interferon-alpha(1) gene transfer on in vivo growth of human breast cancer cells. Gene Ther 9(13):867–878PubMedCrossRef
87.
go back to reference Persano L, Moserle L, Esposito G et al (2009) Interferon-alpha counteracts the angiogenic switch and reduces tumor cell proliferation in a spontaneous model of prostatic cancer. Carcinogenesis 30(5):851–860PubMedCrossRef Persano L, Moserle L, Esposito G et al (2009) Interferon-alpha counteracts the angiogenic switch and reduces tumor cell proliferation in a spontaneous model of prostatic cancer. Carcinogenesis 30(5):851–860PubMedCrossRef
88.
go back to reference Indraccolo S, Pfeffer U, Minuzzo S et al (2007) Identification of genes selectively regulated by IFNs in endothelial cells. J Immunol 178(2):1122–1135PubMed Indraccolo S, Pfeffer U, Minuzzo S et al (2007) Identification of genes selectively regulated by IFNs in endothelial cells. J Immunol 178(2):1122–1135PubMed
89.
go back to reference Kitaya K, Yasuo T, Yamaguchi T et al (2007) Genes regulated by interferon-gamma in human uterine microvascular endothelial cells. Int J Mol Med 20(5):689–697PubMed Kitaya K, Yasuo T, Yamaguchi T et al (2007) Genes regulated by interferon-gamma in human uterine microvascular endothelial cells. Int J Mol Med 20(5):689–697PubMed
90.
go back to reference Sana TR, Janatpour MJ, Sathe M et al (2005) Microarray analysis of primary endothelial cells challenged with different inflammatory and immune cytokines. Cytokine 29(6):256–269PubMed Sana TR, Janatpour MJ, Sathe M et al (2005) Microarray analysis of primary endothelial cells challenged with different inflammatory and immune cytokines. Cytokine 29(6):256–269PubMed
91.
go back to reference Taylor KL, Leaman DW, Grane R et al (2008) Identification of interferon-beta-stimulated genes that inhibit angiogenesis in vitro. J Interferon Cytokine Res 28(12):733–740PubMedCrossRef Taylor KL, Leaman DW, Grane R et al (2008) Identification of interferon-beta-stimulated genes that inhibit angiogenesis in vitro. J Interferon Cytokine Res 28(12):733–740PubMedCrossRef
92.
go back to reference Guenzi E, Topolt K, Lubeseder-Martellato C et al (2003) The guanylate binding protein-1 GTPase controls the invasive and angiogenic capability of endothelial cells through inhibition of MMP-1 expression. EMBO J 22(15):3772–3782PubMedCrossRef Guenzi E, Topolt K, Lubeseder-Martellato C et al (2003) The guanylate binding protein-1 GTPase controls the invasive and angiogenic capability of endothelial cells through inhibition of MMP-1 expression. EMBO J 22(15):3772–3782PubMedCrossRef
93.
go back to reference Lubeseder-Martellato C, Guenzi E, Jorg A et al (2002) Guanylate-binding protein-1 expression is selectively induced by inflammatory cytokines and is an activation marker of endothelial cells during inflammatory diseases. Am J Pathol 161(5):1749–1759PubMed Lubeseder-Martellato C, Guenzi E, Jorg A et al (2002) Guanylate-binding protein-1 expression is selectively induced by inflammatory cytokines and is an activation marker of endothelial cells during inflammatory diseases. Am J Pathol 161(5):1749–1759PubMed
94.
go back to reference Angiolillo AL, Sgadari C, Taub DD et al (1995) Human interferon-inducible protein 10 is a potent inhibitor of angiogenesis in vivo. J Exp Med 182(1):155–162PubMedCrossRef Angiolillo AL, Sgadari C, Taub DD et al (1995) Human interferon-inducible protein 10 is a potent inhibitor of angiogenesis in vivo. J Exp Med 182(1):155–162PubMedCrossRef
95.
go back to reference Sgadari C, Angiolillo AL, Cherney BW et al (1996) Interferon-inducible protein-10 identified as a mediator of tumor necrosis in vivo. Proc Natl Acad Sci USA 93(24):13791–13796PubMedCrossRef Sgadari C, Angiolillo AL, Cherney BW et al (1996) Interferon-inducible protein-10 identified as a mediator of tumor necrosis in vivo. Proc Natl Acad Sci USA 93(24):13791–13796PubMedCrossRef
96.
go back to reference De Bouard S, Guillamo JS, Christov C et al (2003) Antiangiogenic therapy against experimental glioblastoma using genetically engineered cells producing interferon-alpha, angiostatin, or endostatin. Hum Gene Ther 14(9):883–895PubMedCrossRef De Bouard S, Guillamo JS, Christov C et al (2003) Antiangiogenic therapy against experimental glioblastoma using genetically engineered cells producing interferon-alpha, angiostatin, or endostatin. Hum Gene Ther 14(9):883–895PubMedCrossRef
97.
go back to reference Indraccolo S, Moserle L, Tisato V et al (2006) Gene therapy of ovarian cancer with IFN-alpha-producing fibroblasts: comparison of constitutive and inducible vectors. Gene Ther 13(12):953–965PubMedCrossRef Indraccolo S, Moserle L, Tisato V et al (2006) Gene therapy of ovarian cancer with IFN-alpha-producing fibroblasts: comparison of constitutive and inducible vectors. Gene Ther 13(12):953–965PubMedCrossRef
98.
go back to reference Indraccolo S, Tisato V, Tosello V et al (2005) Interferon-alpha gene therapy by lentiviral vectors contrasts ovarian cancer growth through angiogenesis inhibition. Hum Gene Ther 16(8):957–970PubMedCrossRef Indraccolo S, Tisato V, Tosello V et al (2005) Interferon-alpha gene therapy by lentiviral vectors contrasts ovarian cancer growth through angiogenesis inhibition. Hum Gene Ther 16(8):957–970PubMedCrossRef
99.
go back to reference Rozera C, Carlei D, Lollini PL et al (1999) Interferon (IFN)-beta gene transfer into TS/A adenocarcinoma cells and comparison with IFN-alpha: differential effects on tumorigenicity and host response. Am J Pathol 154(4):1211–1222PubMed Rozera C, Carlei D, Lollini PL et al (1999) Interferon (IFN)-beta gene transfer into TS/A adenocarcinoma cells and comparison with IFN-alpha: differential effects on tumorigenicity and host response. Am J Pathol 154(4):1211–1222PubMed
100.
go back to reference Belardelli F, Gresser I, Maury C et al (1983) Antitumor effects of interferon in mice injected with interferon-sensitive and interferon-resistant Friend leukemia cells. III. Inhibition of growth and necrosis of tumors implanted subcutaneously. Int J Cancer 31(5):649–653PubMedCrossRef Belardelli F, Gresser I, Maury C et al (1983) Antitumor effects of interferon in mice injected with interferon-sensitive and interferon-resistant Friend leukemia cells. III. Inhibition of growth and necrosis of tumors implanted subcutaneously. Int J Cancer 31(5):649–653PubMedCrossRef
101.
go back to reference Bergers G, Hanahan D (2008) Modes of resistance to anti-angiogenic therapy. Nat Rev Cancer 8(8):592–603PubMedCrossRef Bergers G, Hanahan D (2008) Modes of resistance to anti-angiogenic therapy. Nat Rev Cancer 8(8):592–603PubMedCrossRef
102.
go back to reference Curnis F, Gasparri A, Sacchi A et al (2005) Targeted delivery of IFNgamma to tumor vessels uncouples antitumor from counterregulatory mechanisms. Cancer Res 65(7):2906–2913PubMedCrossRef Curnis F, Gasparri A, Sacchi A et al (2005) Targeted delivery of IFNgamma to tumor vessels uncouples antitumor from counterregulatory mechanisms. Cancer Res 65(7):2906–2913PubMedCrossRef
103.
go back to reference Tedjarati S, Baker CH, Apte S et al (2002) Synergistic therapy of human ovarian carcinoma implanted orthotopically in nude mice by optimal biological dose of pegylated interferon alpha combined with paclitaxel. Clin Cancer Res 8(7):2413–2422PubMed Tedjarati S, Baker CH, Apte S et al (2002) Synergistic therapy of human ovarian carcinoma implanted orthotopically in nude mice by optimal biological dose of pegylated interferon alpha combined with paclitaxel. Clin Cancer Res 8(7):2413–2422PubMed
104.
go back to reference Samarajiwa SA, Forster S, Auchettl K et al (2009) INTERFEROME: the database of interferon regulated genes. Nucleic Acids Res 37(Database issue):D852–D857 Samarajiwa SA, Forster S, Auchettl K et al (2009) INTERFEROME: the database of interferon regulated genes. Nucleic Acids Res 37(Database issue):D852–D857
105.
go back to reference Kerbel RS, Hawley RG (1995) Interleukin 12: newest member of the antiangiogenesis club. J Natl Cancer Inst 87(8):557–559PubMedCrossRef Kerbel RS, Hawley RG (1995) Interleukin 12: newest member of the antiangiogenesis club. J Natl Cancer Inst 87(8):557–559PubMedCrossRef
106.
go back to reference Sgadari C, Angiolillo AL, Tosato G (1996) Inhibition of angiogenesis by interleukin-12 is mediated by the interferon-inducible protein 10. Blood 87(9):3877–3882PubMed Sgadari C, Angiolillo AL, Tosato G (1996) Inhibition of angiogenesis by interleukin-12 is mediated by the interferon-inducible protein 10. Blood 87(9):3877–3882PubMed
107.
go back to reference Voest EE, Kenyon BM, O’Reilly MS et al (1995) Inhibition of angiogenesis in vivo by interleukin 12. J Natl Cancer Inst 87(8):581–586PubMedCrossRef Voest EE, Kenyon BM, O’Reilly MS et al (1995) Inhibition of angiogenesis in vivo by interleukin 12. J Natl Cancer Inst 87(8):581–586PubMedCrossRef
108.
go back to reference Yao L, Sgadari C, Furuke K et al (1999) Contribution of natural killer cells to inhibition of angiogenesis by interleukin-12. Blood 93(5):1612–1621PubMed Yao L, Sgadari C, Furuke K et al (1999) Contribution of natural killer cells to inhibition of angiogenesis by interleukin-12. Blood 93(5):1612–1621PubMed
109.
go back to reference Shi X, Cao S, Mitsuhashi M et al (2004) Genome-wide analysis of molecular changes in IL-12-induced control of mammary carcinoma via IFN-gamma-independent mechanisms. J Immunol 172(7):4111–4122PubMed Shi X, Cao S, Mitsuhashi M et al (2004) Genome-wide analysis of molecular changes in IL-12-induced control of mammary carcinoma via IFN-gamma-independent mechanisms. J Immunol 172(7):4111–4122PubMed
110.
go back to reference Clark AF, Mellon J, Li XY et al (1999) Inhibition of intraocular tumor growth by topical application of the angiostatic steroid anecortave acetate. Invest Ophthalmol Vis Sci 40(9):2158–2162PubMed Clark AF, Mellon J, Li XY et al (1999) Inhibition of intraocular tumor growth by topical application of the angiostatic steroid anecortave acetate. Invest Ophthalmol Vis Sci 40(9):2158–2162PubMed
111.
go back to reference Parkins CS, Holder AL, Hill SA et al (2000) Determinants of anti-vascular action by combretastatin A-4 phosphate: role of nitric oxide. Br J Cancer 83(6):811–816PubMedCrossRef Parkins CS, Holder AL, Hill SA et al (2000) Determinants of anti-vascular action by combretastatin A-4 phosphate: role of nitric oxide. Br J Cancer 83(6):811–816PubMedCrossRef
112.
go back to reference Ingber D, Fujita T, Kishimoto S et al (1990) Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growth. Nature 348(6301):555–557PubMedCrossRef Ingber D, Fujita T, Kishimoto S et al (1990) Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growth. Nature 348(6301):555–557PubMedCrossRef
113.
go back to reference D’Amato RJ, Loughnan MS, Flynn E et al (1994) Thalidomide is an inhibitor of angiogenesis. Proc Natl Acad Sci USA 91(9):4082–4085PubMedCrossRef D’Amato RJ, Loughnan MS, Flynn E et al (1994) Thalidomide is an inhibitor of angiogenesis. Proc Natl Acad Sci USA 91(9):4082–4085PubMedCrossRef
114.
go back to reference Vacca A, Scavelli C, Montefusco V et al (2005) Thalidomide downregulates angiogenic genes in bone marrow endothelial cells of patients with active multiple myeloma. J Clin Oncol 23(23):5334–5346PubMedCrossRef Vacca A, Scavelli C, Montefusco V et al (2005) Thalidomide downregulates angiogenic genes in bone marrow endothelial cells of patients with active multiple myeloma. J Clin Oncol 23(23):5334–5346PubMedCrossRef
115.
go back to reference Majumdar S, Lamothe B, Aggarwal BB (2002) Thalidomide suppresses NF-kappa B activation induced by TNF and H2O2, but not that activated by ceramide, lipopolysaccharides, or phorbol ester. J Immunol 168(6):2644–2651PubMed Majumdar S, Lamothe B, Aggarwal BB (2002) Thalidomide suppresses NF-kappa B activation induced by TNF and H2O2, but not that activated by ceramide, lipopolysaccharides, or phorbol ester. J Immunol 168(6):2644–2651PubMed
116.
go back to reference Ferrari N, Pfeffer U, Dell’Eva R et al (2005) The transforming growth factor-beta family members bone morphogenetic protein-2 and macrophage inhibitory cytokine-1 as mediators of the antiangiogenic activity of N-(4-hydroxyphenyl)retinamide. Clin Cancer Res 11(12):4610–4619PubMedCrossRef Ferrari N, Pfeffer U, Dell’Eva R et al (2005) The transforming growth factor-beta family members bone morphogenetic protein-2 and macrophage inhibitory cytokine-1 as mediators of the antiangiogenic activity of N-(4-hydroxyphenyl)retinamide. Clin Cancer Res 11(12):4610–4619PubMedCrossRef
117.
go back to reference Costa A, Formelli F, Chiesa F et al (1994) Prospects of chemoprevention of human cancers with the synthetic retinoid fenretinide. Cancer Res 54(7 Suppl):2032s–2037sPubMed Costa A, Formelli F, Chiesa F et al (1994) Prospects of chemoprevention of human cancers with the synthetic retinoid fenretinide. Cancer Res 54(7 Suppl):2032s–2037sPubMed
118.
go back to reference Blackwell KL, Haroon ZA, Shan S et al (2000) Tamoxifen inhibits angiogenesis in estrogen receptor-negative animal models. Clin Cancer Res 6(11):4359–4364PubMed Blackwell KL, Haroon ZA, Shan S et al (2000) Tamoxifen inhibits angiogenesis in estrogen receptor-negative animal models. Clin Cancer Res 6(11):4359–4364PubMed
119.
go back to reference del Carmen Garcia M, olina Wolgien M, da Silva ID, Villanova FE et al (2005) Differential gene expression assessed by cDNA microarray analysis in breast cancer tissue under tamoxifen treatment. Eur J Gynaecol Oncol 26(5):501–504 del Carmen Garcia M, olina Wolgien M, da Silva ID, Villanova FE et al (2005) Differential gene expression assessed by cDNA microarray analysis in breast cancer tissue under tamoxifen treatment. Eur J Gynaecol Oncol 26(5):501–504
120.
go back to reference Itoh T, Karlsberg K, Kijima I et al (2005) Letrozole-, anastrozole-, and tamoxifen-responsive genes in MCF-7aro cells: a microarray approach. Mol Cancer Res 3(4):203–218PubMed Itoh T, Karlsberg K, Kijima I et al (2005) Letrozole-, anastrozole-, and tamoxifen-responsive genes in MCF-7aro cells: a microarray approach. Mol Cancer Res 3(4):203–218PubMed
121.
go back to reference Ferrara N, Hillan KJ, Gerber HP et al (2004) Discovery and development of bevacizumab, an anti-VEGF antibody for treating cancer. Nat Rev Drug Discov 3(5):391–400PubMedCrossRef Ferrara N, Hillan KJ, Gerber HP et al (2004) Discovery and development of bevacizumab, an anti-VEGF antibody for treating cancer. Nat Rev Drug Discov 3(5):391–400PubMedCrossRef
122.
go back to reference Murphy DA, Makonnen S, Lassoued W et al (2006) Inhibition of tumor endothelial ERK activation, angiogenesis, and tumor growth by sorafenib (BAY43–9006). Am J Pathol 169(5):1875–1885PubMedCrossRef Murphy DA, Makonnen S, Lassoued W et al (2006) Inhibition of tumor endothelial ERK activation, angiogenesis, and tumor growth by sorafenib (BAY43–9006). Am J Pathol 169(5):1875–1885PubMedCrossRef
123.
go back to reference Sun L, Liang C, Shirazian S et al (2003) Discovery of 5-[5-fluoro-2-oxo-1, 2- dihydroindol-(3Z)-ylidenemethyl]-2, 4- dimethyl-1H-pyrrole-3-carboxylic acid (2-diethylaminoethyl)amide, a novel tyrosine kinase inhibitor targeting vascular endothelial and platelet-derived growth factor receptor tyrosine kinase. J Med Chem 46(7):1116–1119PubMedCrossRef Sun L, Liang C, Shirazian S et al (2003) Discovery of 5-[5-fluoro-2-oxo-1, 2- dihydroindol-(3Z)-ylidenemethyl]-2, 4- dimethyl-1H-pyrrole-3-carboxylic acid (2-diethylaminoethyl)amide, a novel tyrosine kinase inhibitor targeting vascular endothelial and platelet-derived growth factor receptor tyrosine kinase. J Med Chem 46(7):1116–1119PubMedCrossRef
124.
go back to reference Fischer C, Jonckx B, Mazzone M et al (2007) Anti-PlGF inhibits growth of VEGF(R)-inhibitor-resistant tumors without affecting healthy vessels. Cell 131(3):463–475PubMedCrossRef Fischer C, Jonckx B, Mazzone M et al (2007) Anti-PlGF inhibits growth of VEGF(R)-inhibitor-resistant tumors without affecting healthy vessels. Cell 131(3):463–475PubMedCrossRef
125.
go back to reference Guba M, von Breitenbuch P, Steinbauer M et al (2002) Rapamycin inhibits primary and metastatic tumor growth by antiangiogenesis: involvement of vascular endothelial growth factor. Nat Med 8(2):128–135PubMedCrossRef Guba M, von Breitenbuch P, Steinbauer M et al (2002) Rapamycin inhibits primary and metastatic tumor growth by antiangiogenesis: involvement of vascular endothelial growth factor. Nat Med 8(2):128–135PubMedCrossRef
126.
go back to reference Jia Z, Zhang J, Wei D et al (2007) Molecular basis of the synergistic antiangiogenic activity of bevacizumab and mithramycin A. Cancer Res 67(10):4878–4885PubMedCrossRef Jia Z, Zhang J, Wei D et al (2007) Molecular basis of the synergistic antiangiogenic activity of bevacizumab and mithramycin A. Cancer Res 67(10):4878–4885PubMedCrossRef
127.
go back to reference Yang SX, Steinberg SM, Nguyen D et al (2008) Gene expression profile and angiogenic marker correlates with response to neoadjuvant bevacizumab followed by bevacizumab plus chemotherapy in breast cancer. Clin Cancer Res 14(18):5893–5899PubMedCrossRef Yang SX, Steinberg SM, Nguyen D et al (2008) Gene expression profile and angiogenic marker correlates with response to neoadjuvant bevacizumab followed by bevacizumab plus chemotherapy in breast cancer. Clin Cancer Res 14(18):5893–5899PubMedCrossRef
128.
go back to reference Albini A, Mirisola V, Pfeffer U (2008) Metastasis signatures: genes regulating tumor-microenvironment interactions predict metastatic behavior. Cancer Metastasis Rev 27(1):75–83PubMedCrossRef Albini A, Mirisola V, Pfeffer U (2008) Metastasis signatures: genes regulating tumor-microenvironment interactions predict metastatic behavior. Cancer Metastasis Rev 27(1):75–83PubMedCrossRef
129.
go back to reference Moreno-Vinasco L, Gomberg-Maitland M, Maitland ML et al (2008) Genomic assessment of a multikinase inhibitor, sorafenib, in a rodent model of pulmonary hypertension. Physiol Genomics 33(2):278–291PubMedCrossRef Moreno-Vinasco L, Gomberg-Maitland M, Maitland ML et al (2008) Genomic assessment of a multikinase inhibitor, sorafenib, in a rodent model of pulmonary hypertension. Physiol Genomics 33(2):278–291PubMedCrossRef
130.
go back to reference Newell P, Toffanin S, Villanueva A et al (2009) Ras pathway activation in hepatocellular carcinoma and anti-tumoral effect of combined sorafenib and rapamycin in vivo. J Hepatol 51(4):725–733PubMedCrossRef Newell P, Toffanin S, Villanueva A et al (2009) Ras pathway activation in hepatocellular carcinoma and anti-tumoral effect of combined sorafenib and rapamycin in vivo. J Hepatol 51(4):725–733PubMedCrossRef
131.
go back to reference Kasukabe T, Okabe-Kado J, Kato N et al (2005) Effects of combined treatment with rapamycin and cotylenin A, a novel differentiation-inducing agent, on human breast carcinoma MCF-7 cells and xenografts. Breast Cancer Res 7(6):R1097–R1110PubMedCrossRef Kasukabe T, Okabe-Kado J, Kato N et al (2005) Effects of combined treatment with rapamycin and cotylenin A, a novel differentiation-inducing agent, on human breast carcinoma MCF-7 cells and xenografts. Breast Cancer Res 7(6):R1097–R1110PubMedCrossRef
132.
go back to reference Grolleau A, Bowman J, Pradet-Balade B et al (2002) Global and specific translational control by rapamycin in T cells uncovered by microarrays and proteomics. J Biol Chem 277(25):22175–22184PubMedCrossRef Grolleau A, Bowman J, Pradet-Balade B et al (2002) Global and specific translational control by rapamycin in T cells uncovered by microarrays and proteomics. J Biol Chem 277(25):22175–22184PubMedCrossRef
133.
go back to reference Park IH, Chen J (2005) Mammalian target of rapamycin (mTOR) signaling is required for a late-stage fusion process during skeletal myotube maturation. J Biol Chem 280(36):32009–32017PubMedCrossRef Park IH, Chen J (2005) Mammalian target of rapamycin (mTOR) signaling is required for a late-stage fusion process during skeletal myotube maturation. J Biol Chem 280(36):32009–32017PubMedCrossRef
134.
go back to reference Gera JF, Mellinghoff IK, Shi Y et al (2004) AKT activity determines sensitivity to mammalian target of rapamycin (mTOR) inhibitors by regulating cyclin D1 and c-myc expression. J Biol Chem 279(4):2737–2746PubMedCrossRef Gera JF, Mellinghoff IK, Shi Y et al (2004) AKT activity determines sensitivity to mammalian target of rapamycin (mTOR) inhibitors by regulating cyclin D1 and c-myc expression. J Biol Chem 279(4):2737–2746PubMedCrossRef
135.
go back to reference van de Vijver MJ, He YD, van’t Veer LJ et al (2002) A gene-expression signature as a predictor of survival in breast cancer. N Engl J Med 347(25):1999–2009PubMedCrossRef van de Vijver MJ, He YD, van’t Veer LJ et al (2002) A gene-expression signature as a predictor of survival in breast cancer. N Engl J Med 347(25):1999–2009PubMedCrossRef
136.
go back to reference Ramaswamy S, Ross KN, Lander ES et al (2003) A molecular signature of metastasis in primary solid tumors. Nat Genet 33(1):49–54PubMedCrossRef Ramaswamy S, Ross KN, Lander ES et al (2003) A molecular signature of metastasis in primary solid tumors. Nat Genet 33(1):49–54PubMedCrossRef
137.
go back to reference Webb T (2003) Microarray studies challenge theories of metastasis. J Natl Cancer Inst 95(5):350–351PubMedCrossRef Webb T (2003) Microarray studies challenge theories of metastasis. J Natl Cancer Inst 95(5):350–351PubMedCrossRef
139.
go back to reference Pfeffer U, Noonan D, Albini A (2003) Re: microarray studies challenge theories of metastasis. J Natl Cancer Inst 95(11):829PubMed Pfeffer U, Noonan D, Albini A (2003) Re: microarray studies challenge theories of metastasis. J Natl Cancer Inst 95(11):829PubMed
140.
go back to reference Albini A, Morini M, D’Agostini F et al (2001) Inhibition of angiogenesis-driven Kaposi’s sarcoma tumor growth in nude mice by oral N-acetylcysteine. Cancer Res 61(22):8171–8178PubMed Albini A, Morini M, D’Agostini F et al (2001) Inhibition of angiogenesis-driven Kaposi’s sarcoma tumor growth in nude mice by oral N-acetylcysteine. Cancer Res 61(22):8171–8178PubMed
141.
go back to reference Garbisa S, Biggin S, Cavallarin N et al (1999) Tumor invasion: molecular shears blunted by green tea. Nat Med 5(11):1216PubMedCrossRef Garbisa S, Biggin S, Cavallarin N et al (1999) Tumor invasion: molecular shears blunted by green tea. Nat Med 5(11):1216PubMedCrossRef
142.
go back to reference Yu YM, Wang ZH, Liu CH et al (2007) Ellagic acid inhibits IL-1beta-induced cell adhesion molecule expression in human umbilical vein endothelial cells. Br J Nutr 97(4):692–698PubMedCrossRef Yu YM, Wang ZH, Liu CH et al (2007) Ellagic acid inhibits IL-1beta-induced cell adhesion molecule expression in human umbilical vein endothelial cells. Br J Nutr 97(4):692–698PubMedCrossRef
143.
go back to reference Kumar A, Dhawan S, Hardegen NJ et al (1998) Curcumin (Diferuloylmethane) inhibition of tumor necrosis factor (TNF)-mediated adhesion of monocytes to endothelial cells by suppression of cell surface expression of adhesion molecules and of nuclear factor-kappaB activation. Biochem Pharmacol 55(6):775–783PubMedCrossRef Kumar A, Dhawan S, Hardegen NJ et al (1998) Curcumin (Diferuloylmethane) inhibition of tumor necrosis factor (TNF)-mediated adhesion of monocytes to endothelial cells by suppression of cell surface expression of adhesion molecules and of nuclear factor-kappaB activation. Biochem Pharmacol 55(6):775–783PubMedCrossRef
144.
go back to reference Lorusso G, Vannini N, Sogno I et al (2009) Mechanisms of Hyperforin as an anti-angiogenic angioprevention agent. Eur J Cancer 45(8):1474–1484PubMedCrossRef Lorusso G, Vannini N, Sogno I et al (2009) Mechanisms of Hyperforin as an anti-angiogenic angioprevention agent. Eur J Cancer 45(8):1474–1484PubMedCrossRef
145.
go back to reference Khachigian LM, Collins T, Fries JW (1997) N-acetyl cysteine blocks mesangial VCAM-1 and NF-kappa B expression in vivo. Am J Pathol 151(5):1225–1229PubMed Khachigian LM, Collins T, Fries JW (1997) N-acetyl cysteine blocks mesangial VCAM-1 and NF-kappa B expression in vivo. Am J Pathol 151(5):1225–1229PubMed
146.
go back to reference Sethi G, Ahn KS, Sung B et al (2008) Pinitol targets nuclear factor-kappaB activation pathway leading to inhibition of gene products associated with proliferation, apoptosis, invasion, and angiogenesis. Mol Cancer Ther 7(6):1604–1614PubMedCrossRef Sethi G, Ahn KS, Sung B et al (2008) Pinitol targets nuclear factor-kappaB activation pathway leading to inhibition of gene products associated with proliferation, apoptosis, invasion, and angiogenesis. Mol Cancer Ther 7(6):1604–1614PubMedCrossRef
147.
go back to reference Ahmad R, Raina D, Meyer C et al (2006) Triterpenoid CDDO-Me blocks the NF-kappaB pathway by direct inhibition of IKKbeta on Cys-179. J Biol Chem 281(47):35764–35769PubMedCrossRef Ahmad R, Raina D, Meyer C et al (2006) Triterpenoid CDDO-Me blocks the NF-kappaB pathway by direct inhibition of IKKbeta on Cys-179. J Biol Chem 281(47):35764–35769PubMedCrossRef
148.
go back to reference Albini A, Dell’Eva R, Vene R et al (2006) Mechanisms of the antiangiogenic activity by the hop flavonoid xanthohumol: NF-kappaB and Akt as targets. FASEB J 20(3):527–529PubMed Albini A, Dell’Eva R, Vene R et al (2006) Mechanisms of the antiangiogenic activity by the hop flavonoid xanthohumol: NF-kappaB and Akt as targets. FASEB J 20(3):527–529PubMed
149.
go back to reference Lapillonne H, Konopleva M, Tsao T et al (2003) Activation of peroxisome proliferator-activated receptor gamma by a novel synthetic triterpenoid 2-cyano-3, 12-dioxooleana-1, 9-dien-28-oic acid induces growth arrest and apoptosis in breast cancer cells. Cancer Res 63(18):5926–5939PubMed Lapillonne H, Konopleva M, Tsao T et al (2003) Activation of peroxisome proliferator-activated receptor gamma by a novel synthetic triterpenoid 2-cyano-3, 12-dioxooleana-1, 9-dien-28-oic acid induces growth arrest and apoptosis in breast cancer cells. Cancer Res 63(18):5926–5939PubMed
150.
go back to reference Ahmad R, Raina D, Meyer C et al (2008) Triterpenoid CDDO-methyl ester inhibits the Janus-activated kinase-1 (JAK1)– >signal transducer and activator of transcription-3 (STAT3) pathway by direct inhibition of JAK1 and STAT3. Cancer Res 68(8):2920–2926PubMedCrossRef Ahmad R, Raina D, Meyer C et al (2008) Triterpenoid CDDO-methyl ester inhibits the Janus-activated kinase-1 (JAK1)– >signal transducer and activator of transcription-3 (STAT3) pathway by direct inhibition of JAK1 and STAT3. Cancer Res 68(8):2920–2926PubMedCrossRef
151.
go back to reference Sussan TE, Rangasamy T, Blake DJ et al (2009) Targeting Nrf2 with the triterpenoid CDDO-imidazolide attenuates cigarette smoke-induced emphysema and cardiac dysfunction in mice. Proc Natl Acad Sci USA 106(1):250–255PubMedCrossRef Sussan TE, Rangasamy T, Blake DJ et al (2009) Targeting Nrf2 with the triterpenoid CDDO-imidazolide attenuates cigarette smoke-induced emphysema and cardiac dysfunction in mice. Proc Natl Acad Sci USA 106(1):250–255PubMedCrossRef
152.
go back to reference Chen HH, Zhou HJ, Wu GD et al (2004) Inhibitory effects of artesunate on angiogenesis and on expressions of vascular endothelial growth factor and VEGF receptor KDR/flk-1. Pharmacology 71(1):1–9PubMedCrossRef Chen HH, Zhou HJ, Wu GD et al (2004) Inhibitory effects of artesunate on angiogenesis and on expressions of vascular endothelial growth factor and VEGF receptor KDR/flk-1. Pharmacology 71(1):1–9PubMedCrossRef
153.
go back to reference Pang X, Yi Z, Zhang X et al (2009) Acetyl-11-keto-beta-boswellic acid inhibits prostate tumor growth by suppressing vascular endothelial growth factor receptor 2-mediated angiogenesis. Cancer Res 69(14):5893–5900PubMedCrossRef Pang X, Yi Z, Zhang X et al (2009) Acetyl-11-keto-beta-boswellic acid inhibits prostate tumor growth by suppressing vascular endothelial growth factor receptor 2-mediated angiogenesis. Cancer Res 69(14):5893–5900PubMedCrossRef
154.
go back to reference Yi T, Yi Z, Cho SG et al (2008) Gambogic acid inhibits angiogenesis and prostate tumor growth by suppressing vascular endothelial growth factor receptor 2 signaling. Cancer Res 68(6):1843–1850PubMedCrossRef Yi T, Yi Z, Cho SG et al (2008) Gambogic acid inhibits angiogenesis and prostate tumor growth by suppressing vascular endothelial growth factor receptor 2 signaling. Cancer Res 68(6):1843–1850PubMedCrossRef
155.
go back to reference Larghero P, Vene R, Minghelli S et al (2007) Biological assays and genomic analysis reveal lipoic acid modulation of endothelial cell behavior and gene expression. Carcinogenesis 28(5):1008–1020PubMedCrossRef Larghero P, Vene R, Minghelli S et al (2007) Biological assays and genomic analysis reveal lipoic acid modulation of endothelial cell behavior and gene expression. Carcinogenesis 28(5):1008–1020PubMedCrossRef
156.
go back to reference Park MJ, Kim EH, Park IC et al (2002) Curcumin inhibits cell cycle progression of immortalized human umbilical vein endothelial (ECV304) cells by up-regulating cyclin-dependent kinase inhibitor, p21WAF1/CIP1, p27KIP1 and p53. Int J Oncol 21(2):379–383PubMed Park MJ, Kim EH, Park IC et al (2002) Curcumin inhibits cell cycle progression of immortalized human umbilical vein endothelial (ECV304) cells by up-regulating cyclin-dependent kinase inhibitor, p21WAF1/CIP1, p27KIP1 and p53. Int J Oncol 21(2):379–383PubMed
157.
go back to reference Stierum R, Conesa A, Heijne W et al (2008) Transcriptome analysis provides new insights into liver changes induced in the rat upon dietary administration of the food additives butylated hydroxytoluene, curcumin, propyl gallate and thiabendazole. Food Chem Toxicol 46(8):2616–2628PubMedCrossRef Stierum R, Conesa A, Heijne W et al (2008) Transcriptome analysis provides new insights into liver changes induced in the rat upon dietary administration of the food additives butylated hydroxytoluene, curcumin, propyl gallate and thiabendazole. Food Chem Toxicol 46(8):2616–2628PubMedCrossRef
158.
go back to reference Meng Q, Velalar CN, Ruan R (2008) Regulating the age-related oxidative damage, mitochondrial integrity, and antioxidative enzyme activity in Fischer 344 rats by supplementation of the antioxidant epigallocatechin-3-gallate. Rejuvenation Res 11(3):649–660PubMedCrossRef Meng Q, Velalar CN, Ruan R (2008) Regulating the age-related oxidative damage, mitochondrial integrity, and antioxidative enzyme activity in Fischer 344 rats by supplementation of the antioxidant epigallocatechin-3-gallate. Rejuvenation Res 11(3):649–660PubMedCrossRef
159.
go back to reference Thangapazham RL, Passi N, Maheshwari RK (2007) Green tea polyphenol and epigallocatechin gallate induce apoptosis and inhibit invasion in human breast cancer cells. Cancer Biol Ther 6(12):1938–1943PubMedCrossRef Thangapazham RL, Passi N, Maheshwari RK (2007) Green tea polyphenol and epigallocatechin gallate induce apoptosis and inhibit invasion in human breast cancer cells. Cancer Biol Ther 6(12):1938–1943PubMedCrossRef
160.
go back to reference Shen G, Xu C, Hu R et al (2005) Comparison of (−)-epigallocatechin-3-gallate elicited liver and small intestine gene expression profiles between C57BL/6 J mice and C57BL/6 J/Nrf2 (−/−) mice. Pharm Res 22(11):1805–1820PubMedCrossRef Shen G, Xu C, Hu R et al (2005) Comparison of (−)-epigallocatechin-3-gallate elicited liver and small intestine gene expression profiles between C57BL/6 J mice and C57BL/6 J/Nrf2 (−/−) mice. Pharm Res 22(11):1805–1820PubMedCrossRef
161.
go back to reference Guo S, Yang S, Taylor C et al (2005) Green tea polyphenol epigallocatechin-3 gallate (EGCG) affects gene expression of breast cancer cells transformed by the carcinogen 7, 12-dimethylbenz[a]anthracene. J Nutr 135(12 Suppl):2978S–2986SPubMed Guo S, Yang S, Taylor C et al (2005) Green tea polyphenol epigallocatechin-3 gallate (EGCG) affects gene expression of breast cancer cells transformed by the carcinogen 7, 12-dimethylbenz[a]anthracene. J Nutr 135(12 Suppl):2978S–2986SPubMed
162.
go back to reference Guo S, Lu J, Subramanian A et al (2006) Microarray-assisted pathway analysis identifies mitogen-activated protein kinase signaling as a mediator of resistance to the green tea polyphenol epigallocatechin 3-gallate in her-2/neu-overexpressing breast cancer cells. Cancer Res 66(10):5322–5329PubMedCrossRef Guo S, Lu J, Subramanian A et al (2006) Microarray-assisted pathway analysis identifies mitogen-activated protein kinase signaling as a mediator of resistance to the green tea polyphenol epigallocatechin 3-gallate in her-2/neu-overexpressing breast cancer cells. Cancer Res 66(10):5322–5329PubMedCrossRef
163.
go back to reference Bae JY, Kanamune J, Han DW et al (2009) Reversible regulation of cell cycle-related genes by epigallocatechin gallate for hibernation of neonatal human tarsal fibroblasts. Cell Transplant 18(4):459–469PubMedCrossRef Bae JY, Kanamune J, Han DW et al (2009) Reversible regulation of cell cycle-related genes by epigallocatechin gallate for hibernation of neonatal human tarsal fibroblasts. Cell Transplant 18(4):459–469PubMedCrossRef
164.
go back to reference Hsu S, Dickinson DP, Qin H et al (2005) Inhibition of autoantigen expression by (−)-epigallocatechin-3-gallate (the major constituent of green tea) in normal human cells. J Pharmacol Exp Ther 315(2):805–811PubMedCrossRef Hsu S, Dickinson DP, Qin H et al (2005) Inhibition of autoantigen expression by (−)-epigallocatechin-3-gallate (the major constituent of green tea) in normal human cells. J Pharmacol Exp Ther 315(2):805–811PubMedCrossRef
165.
go back to reference Wolfram S, Raederstorff D, Preller M et al (2006) Epigallocatechin gallate supplementation alleviates diabetes in rodents. J Nutr 136(10):2512–2518PubMed Wolfram S, Raederstorff D, Preller M et al (2006) Epigallocatechin gallate supplementation alleviates diabetes in rodents. J Nutr 136(10):2512–2518PubMed
166.
go back to reference Nones K, Dommels YE, Martell S et al (2009) The effects of dietary curcumin and rutin on colonic inflammation and gene expression in multidrug resistance gene-deficient (mdr1a−/−) mice, a model of inflammatory bowel diseases. Br J Nutr 101(2):169–181PubMedCrossRef Nones K, Dommels YE, Martell S et al (2009) The effects of dietary curcumin and rutin on colonic inflammation and gene expression in multidrug resistance gene-deficient (mdr1a−/−) mice, a model of inflammatory bowel diseases. Br J Nutr 101(2):169–181PubMedCrossRef
167.
go back to reference Sun M, Estrov Z, Ji Y et al (2008) Curcumin (diferuloylmethane) alters the expression profiles of microRNAs in human pancreatic cancer cells. Mol Cancer Ther 7(3):464–473PubMedCrossRef Sun M, Estrov Z, Ji Y et al (2008) Curcumin (diferuloylmethane) alters the expression profiles of microRNAs in human pancreatic cancer cells. Mol Cancer Ther 7(3):464–473PubMedCrossRef
168.
go back to reference Su CC, Chen GW, Lin JG et al (2006) Curcumin inhibits cell migration of human colon cancer colo 205 cells through the inhibition of nuclear factor kappa B/p65 and down-regulates cyclooxygenase-2 and matrix metalloproteinase-2 expressions. Anticancer Res 26(2A):1281–1288 Su CC, Chen GW, Lin JG et al (2006) Curcumin inhibits cell migration of human colon cancer colo 205 cells through the inhibition of nuclear factor kappa B/p65 and down-regulates cyclooxygenase-2 and matrix metalloproteinase-2 expressions. Anticancer Res 26(2A):1281–1288
169.
go back to reference Ramachandran C, Rodriguez S, Ramachandran R et al (2005) Expression profiles of apoptotic genes induced by curcumin in human breast cancer and mammary epithelial cell lines. Anticancer Res 25(5):3293–3302PubMed Ramachandran C, Rodriguez S, Ramachandran R et al (2005) Expression profiles of apoptotic genes induced by curcumin in human breast cancer and mammary epithelial cell lines. Anticancer Res 25(5):3293–3302PubMed
170.
go back to reference Bachmeier BE, Mohrenz IV, Mirisola V et al (2008) Curcumin downregulates the inflammatory cytokines CXCL1 and -2 in breast cancer cells via NFkappaB. Carcinogenesis 29(4):779–789PubMedCrossRef Bachmeier BE, Mohrenz IV, Mirisola V et al (2008) Curcumin downregulates the inflammatory cytokines CXCL1 and -2 in breast cancer cells via NFkappaB. Carcinogenesis 29(4):779–789PubMedCrossRef
171.
go back to reference Bachmeier B, Nerlich AG, Iancu CM et al (2007) The chemopreventive polyphenol Curcumin prevents hematogenous breast cancer metastases in immunodeficient mice. Cell Physiol Biochem 19(1–4):137–152PubMedCrossRef Bachmeier B, Nerlich AG, Iancu CM et al (2007) The chemopreventive polyphenol Curcumin prevents hematogenous breast cancer metastases in immunodeficient mice. Cell Physiol Biochem 19(1–4):137–152PubMedCrossRef
172.
go back to reference Arbiser JL, Klauber N, Rohan R et al (1998) Curcumin is an in vivo inhibitor of angiogenesis. Mol Med 4(6):376–383PubMed Arbiser JL, Klauber N, Rohan R et al (1998) Curcumin is an in vivo inhibitor of angiogenesis. Mol Med 4(6):376–383PubMed
173.
go back to reference Dell’Eva R, Pfeffer U, Vene R et al (2004) Inhibition of angiogenesis in vivo and growth of Kaposi’s sarcoma xenograft tumors by the anti-malarial artesunate. Biochem Pharmacol 68(12):2359–2366PubMedCrossRef Dell’Eva R, Pfeffer U, Vene R et al (2004) Inhibition of angiogenesis in vivo and growth of Kaposi’s sarcoma xenograft tumors by the anti-malarial artesunate. Biochem Pharmacol 68(12):2359–2366PubMedCrossRef
174.
go back to reference Anfosso L, Efferth T, Albini A et al (2006) Microarray expression profiles of angiogenesis-related genes predict tumor cell response to artemisinins. Pharmacogenomics J 6(4):269–278PubMed Anfosso L, Efferth T, Albini A et al (2006) Microarray expression profiles of angiogenesis-related genes predict tumor cell response to artemisinins. Pharmacogenomics J 6(4):269–278PubMed
175.
go back to reference Gonzalez-Sarrias A, Espin JC, Tomas-Barberan FA et al (2009) Gene expression, cell cycle arrest and MAPK signalling regulation in Caco-2 cells exposed to ellagic acid and its metabolites, urolithins. Mol Nutr Food Res 53(6):686–698PubMedCrossRef Gonzalez-Sarrias A, Espin JC, Tomas-Barberan FA et al (2009) Gene expression, cell cycle arrest and MAPK signalling regulation in Caco-2 cells exposed to ellagic acid and its metabolites, urolithins. Mol Nutr Food Res 53(6):686–698PubMedCrossRef
176.
go back to reference Gu H, You Q, Liu W et al (2008) Gambogic acid induced tumor cell apoptosis by T lymphocyte activation in H22 transplanted mice. Int Immunopharmacol 8(11):1493–1502PubMedCrossRef Gu H, You Q, Liu W et al (2008) Gambogic acid induced tumor cell apoptosis by T lymphocyte activation in H22 transplanted mice. Int Immunopharmacol 8(11):1493–1502PubMedCrossRef
177.
go back to reference Krusekopf S, Roots I (2005) St. John’s wort and its constituent hyperforin concordantly regulate expression of genes encoding enzymes involved in basic cellular pathways. Pharmacogenet Genomics 15(11):817–829 Krusekopf S, Roots I (2005) St. John’s wort and its constituent hyperforin concordantly regulate expression of genes encoding enzymes involved in basic cellular pathways. Pharmacogenet Genomics 15(11):817–829
178.
go back to reference Vannini N, Lorusso G, Cammarota R et al (2007) The synthetic oleanane triterpenoid, CDDO-methyl ester, is a potent antiangiogenic agent. Mol Cancer Ther 6(12 Pt 1):3139–3146 Vannini N, Lorusso G, Cammarota R et al (2007) The synthetic oleanane triterpenoid, CDDO-methyl ester, is a potent antiangiogenic agent. Mol Cancer Ther 6(12 Pt 1):3139–3146
179.
go back to reference Yates MS, Kwak MK, Egner PA et al (2006) Potent protection against aflatoxin-induced tumorigenesis through induction of Nrf2-regulated pathways by the triterpenoid 1-[2-cyano-3-, 12-dioxooleana-1, 9(11)-dien-28-oyl]imidazole. Cancer Res 66(4):2488–2494PubMedCrossRef Yates MS, Kwak MK, Egner PA et al (2006) Potent protection against aflatoxin-induced tumorigenesis through induction of Nrf2-regulated pathways by the triterpenoid 1-[2-cyano-3-, 12-dioxooleana-1, 9(11)-dien-28-oyl]imidazole. Cancer Res 66(4):2488–2494PubMedCrossRef
180.
go back to reference Das A, Mantena SR, Kannan A et al (2009) De novo synthesis of estrogen in pregnant uterus is critical for stromal decidualization and angiogenesis. Proc Natl Acad Sci USA 106(30):12542–12547PubMedCrossRef Das A, Mantena SR, Kannan A et al (2009) De novo synthesis of estrogen in pregnant uterus is critical for stromal decidualization and angiogenesis. Proc Natl Acad Sci USA 106(30):12542–12547PubMedCrossRef
181.
go back to reference Seo KH, Lee HS, Jung B et al (2004) Estrogen enhances angiogenesis through a pathway involving platelet-activating factor-mediated nuclear factor-kappaB activation. Cancer Res 64(18):6482–6488PubMedCrossRef Seo KH, Lee HS, Jung B et al (2004) Estrogen enhances angiogenesis through a pathway involving platelet-activating factor-mediated nuclear factor-kappaB activation. Cancer Res 64(18):6482–6488PubMedCrossRef
182.
go back to reference Johns A, Freay AD, Fraser W et al (1996) Disruption of estrogen receptor gene prevents 17 beta estradiol-induced angiogenesis in transgenic mice. Endocrinology 137(10):4511–4513PubMedCrossRef Johns A, Freay AD, Fraser W et al (1996) Disruption of estrogen receptor gene prevents 17 beta estradiol-induced angiogenesis in transgenic mice. Endocrinology 137(10):4511–4513PubMedCrossRef
183.
go back to reference Chen Y, Jin X, Zeng Z et al (2009) Estrogen-replacement therapy promotes angiogenesis after acute myocardial infarction by enhancing SDF-1 and estrogen receptor expression. Microvasc Res 77(2):71–77PubMedCrossRef Chen Y, Jin X, Zeng Z et al (2009) Estrogen-replacement therapy promotes angiogenesis after acute myocardial infarction by enhancing SDF-1 and estrogen receptor expression. Microvasc Res 77(2):71–77PubMedCrossRef
184.
go back to reference Hartman J, Lindberg K, Morani A et al (2006) Estrogen receptor beta inhibits angiogenesis and growth of T47D breast cancer xenografts. Cancer Res 66(23):11207–11213PubMedCrossRef Hartman J, Lindberg K, Morani A et al (2006) Estrogen receptor beta inhibits angiogenesis and growth of T47D breast cancer xenografts. Cancer Res 66(23):11207–11213PubMedCrossRef
185.
go back to reference Beral V (1997) Breast cancer and hormone replacement therapy: collaborative reanalysis of data from 51 epidemiological studies of 52,705 women with breast cancer and 108,411 women without breast cancer. Collaborative group on hormonal factors in breast cancer. Lancet 350(9084):1047–1059 Beral V (1997) Breast cancer and hormone replacement therapy: collaborative reanalysis of data from 51 epidemiological studies of 52,705 women with breast cancer and 108,411 women without breast cancer. Collaborative group on hormonal factors in breast cancer. Lancet 350(9084):1047–1059
186.
go back to reference Fotsis T, Pepper M, Adlercreutz H et al (1993) Genistein, a dietary-derived inhibitor of in vitro angiogenesis. Proc Natl Acad Sci USA 90(7):2690–2694PubMedCrossRef Fotsis T, Pepper M, Adlercreutz H et al (1993) Genistein, a dietary-derived inhibitor of in vitro angiogenesis. Proc Natl Acad Sci USA 90(7):2690–2694PubMedCrossRef
187.
go back to reference Ambra R, Rimbach G, de Pascual Teresa S et al (2006) Genistein affects the expression of genes involved in blood pressure regulation and angiogenesis in primary human endothelial cells. Nutr Metab Cardiovasc Dis 16(1):35–43PubMedCrossRef Ambra R, Rimbach G, de Pascual Teresa S et al (2006) Genistein affects the expression of genes involved in blood pressure regulation and angiogenesis in primary human endothelial cells. Nutr Metab Cardiovasc Dis 16(1):35–43PubMedCrossRef
188.
go back to reference Piao M, Mori D, Satoh T et al (2006) Inhibition of endothelial cell proliferation, in vitro angiogenesis, and the down-regulation of cell adhesion-related genes by genistein. Combined with a cDNA microarray analysis. Endothelium 13(4):249–266 Piao M, Mori D, Satoh T et al (2006) Inhibition of endothelial cell proliferation, in vitro angiogenesis, and the down-regulation of cell adhesion-related genes by genistein. Combined with a cDNA microarray analysis. Endothelium 13(4):249–266
189.
go back to reference Li Y, Sarkar FH (2002) Gene expression profiles of genistein-treated PC3 prostate cancer cells. J Nutr 132(12):3623–3631PubMed Li Y, Sarkar FH (2002) Gene expression profiles of genistein-treated PC3 prostate cancer cells. J Nutr 132(12):3623–3631PubMed
190.
go back to reference Suzuki K, Koike H, Matsui H et al (2002) Genistein, a soy isoflavone, induces glutathione peroxidase in the human prostate cancer cell lines LNCaP and PC-3. Int J Cancer 99(6):846–852PubMedCrossRef Suzuki K, Koike H, Matsui H et al (2002) Genistein, a soy isoflavone, induces glutathione peroxidase in the human prostate cancer cell lines LNCaP and PC-3. Int J Cancer 99(6):846–852PubMedCrossRef
191.
go back to reference Li Y, Kucuk O, Hussain M et al (2006) Antitumor and antimetastatic activities of docetaxel are enhanced by genistein through regulation of osteoprotegerin/receptor activator of nuclear factor-kappaB (RANK)/RANK ligand/MMP-9 signaling in prostate cancer. Cancer Res 66(9):4816–4825PubMedCrossRef Li Y, Kucuk O, Hussain M et al (2006) Antitumor and antimetastatic activities of docetaxel are enhanced by genistein through regulation of osteoprotegerin/receptor activator of nuclear factor-kappaB (RANK)/RANK ligand/MMP-9 signaling in prostate cancer. Cancer Res 66(9):4816–4825PubMedCrossRef
192.
go back to reference Li Y, Che M, Bhagat S et al (2004) Regulation of gene expression and inhibition of experimental prostate cancer bone metastasis by dietary genistein. Neoplasia 6(4):354–363PubMedCrossRef Li Y, Che M, Bhagat S et al (2004) Regulation of gene expression and inhibition of experimental prostate cancer bone metastasis by dietary genistein. Neoplasia 6(4):354–363PubMedCrossRef
193.
go back to reference Bai J, Sata N, Nagai H et al (2004) Genistein-induced changes in gene expression in Panc 1 cells at physiological concentrations of genistein. Pancreas 29(2):93–98PubMedCrossRef Bai J, Sata N, Nagai H et al (2004) Genistein-induced changes in gene expression in Panc 1 cells at physiological concentrations of genistein. Pancreas 29(2):93–98PubMedCrossRef
194.
go back to reference Takahashi Y, Odbayar TO, Ide T (2009) A comparative analysis of genistein and daidzein in affecting lipid metabolism in rat liver. J Clin Biochem Nutr 44(3):223–230PubMedCrossRef Takahashi Y, Odbayar TO, Ide T (2009) A comparative analysis of genistein and daidzein in affecting lipid metabolism in rat liver. J Clin Biochem Nutr 44(3):223–230PubMedCrossRef
195.
go back to reference Zou H, Zhan S, Cao K (2008) Apoptotic activity of genistein on human lung adenocarcinoma SPC-A-1 cells and preliminary exploration of its mechanisms using microarray. Biomed Pharmacother 62(9):583–589PubMedCrossRef Zou H, Zhan S, Cao K (2008) Apoptotic activity of genistein on human lung adenocarcinoma SPC-A-1 cells and preliminary exploration of its mechanisms using microarray. Biomed Pharmacother 62(9):583–589PubMedCrossRef
196.
go back to reference Lee WY, Huang SC, Tzeng CC et al (2007) Alterations of metastasis-related genes identified using an oligonucleotide microarray of genistein-treated HCC1395 breast cancer cells. Nutr Cancer 58(2):239–246PubMed Lee WY, Huang SC, Tzeng CC et al (2007) Alterations of metastasis-related genes identified using an oligonucleotide microarray of genistein-treated HCC1395 breast cancer cells. Nutr Cancer 58(2):239–246PubMed
197.
go back to reference Penza M, Montani C, Romani A et al (2006) Genistein affects adipose tissue deposition in a dose-dependent and gender-specific manner. Endocrinology 147(12):5740–5751PubMedCrossRef Penza M, Montani C, Romani A et al (2006) Genistein affects adipose tissue deposition in a dose-dependent and gender-specific manner. Endocrinology 147(12):5740–5751PubMedCrossRef
198.
go back to reference Cooke PS, Selvaraj V, Yellayi S (2006) Genistein, estrogen receptors, and the acquired immune response. J Nutr 136(3):704–708PubMed Cooke PS, Selvaraj V, Yellayi S (2006) Genistein, estrogen receptors, and the acquired immune response. J Nutr 136(3):704–708PubMed
199.
go back to reference Wang XJ, Bartolucci-Page E, Fenton SE et al (2006) Altered mammary gland development in male rats exposed to genistein and methoxychlor. Toxicol Sci 91(1):93–103PubMedCrossRef Wang XJ, Bartolucci-Page E, Fenton SE et al (2006) Altered mammary gland development in male rats exposed to genistein and methoxychlor. Toxicol Sci 91(1):93–103PubMedCrossRef
200.
go back to reference Lavigne JA, Takahashi Y, Chandramouli GV et al (2008) Concentration-dependent effects of genistein on global gene expression in MCF-7 breast cancer cells: an oligo microarray study. Breast Cancer Res Treat 110(1):85–98PubMedCrossRef Lavigne JA, Takahashi Y, Chandramouli GV et al (2008) Concentration-dependent effects of genistein on global gene expression in MCF-7 breast cancer cells: an oligo microarray study. Breast Cancer Res Treat 110(1):85–98PubMedCrossRef
201.
go back to reference Konstantakopoulos N, Montgomery KG, Chamberlain N et al (2006) Changes in gene expressions elicited by physiological concentrations of genistein on human endometrial cancer cells. Mol Carcinog 45(10):752–763PubMedCrossRef Konstantakopoulos N, Montgomery KG, Chamberlain N et al (2006) Changes in gene expressions elicited by physiological concentrations of genistein on human endometrial cancer cells. Mol Carcinog 45(10):752–763PubMedCrossRef
202.
go back to reference Igura K, Ohta T, Kuroda Y et al (2001) Resveratrol and quercetin inhibit angiogenesis in vitro. Cancer Lett 171(1):11–16PubMedCrossRef Igura K, Ohta T, Kuroda Y et al (2001) Resveratrol and quercetin inhibit angiogenesis in vitro. Cancer Lett 171(1):11–16PubMedCrossRef
203.
go back to reference Gehm BD, McAndrews JM, Chien PY et al (1997) Resveratrol, a polyphenolic compound found in grapes and wine, is an agonist for the estrogen receptor. Proc Natl Acad Sci USA 94(25):14138–14143PubMedCrossRef Gehm BD, McAndrews JM, Chien PY et al (1997) Resveratrol, a polyphenolic compound found in grapes and wine, is an agonist for the estrogen receptor. Proc Natl Acad Sci USA 94(25):14138–14143PubMedCrossRef
204.
go back to reference Scambia G, Ranelletti FO, Benedetti Panici P et al (1991) Quercetin inhibits the growth of a multidrug-resistant estrogen-receptor-negative MCF-7 human breast-cancer cell line expressing type II estrogen-binding sites. Cancer Chemother Pharmacol 28(4):255–258PubMed Scambia G, Ranelletti FO, Benedetti Panici P et al (1991) Quercetin inhibits the growth of a multidrug-resistant estrogen-receptor-negative MCF-7 human breast-cancer cell line expressing type II estrogen-binding sites. Cancer Chemother Pharmacol 28(4):255–258PubMed
205.
go back to reference van der Woude H, Ter Veld MG, Jacobs N et al (2005) The stimulation of cell proliferation by quercetin is mediated by the estrogen receptor. Mol Nutr Food Res 49(8):763–771PubMedCrossRef van der Woude H, Ter Veld MG, Jacobs N et al (2005) The stimulation of cell proliferation by quercetin is mediated by the estrogen receptor. Mol Nutr Food Res 49(8):763–771PubMedCrossRef
206.
go back to reference Woodall BP, Nystrom A, Iozzo RA et al (2008) Integrin alpha2beta1 is the required receptor for endorepellin angiostatic activity. J Biol Chem 283(4):2335–2343PubMedCrossRef Woodall BP, Nystrom A, Iozzo RA et al (2008) Integrin alpha2beta1 is the required receptor for endorepellin angiostatic activity. J Biol Chem 283(4):2335–2343PubMedCrossRef
207.
go back to reference Ambesi A, Klein RM, Pumiglia KM et al (2005) Anastellin, a fragment of the first type III repeat of fibronectin, inhibits extracellular signal-regulated kinase and causes G(1) arrest in human microvessel endothelial cells. Cancer Res 65(1):148–156PubMed Ambesi A, Klein RM, Pumiglia KM et al (2005) Anastellin, a fragment of the first type III repeat of fibronectin, inhibits extracellular signal-regulated kinase and causes G(1) arrest in human microvessel endothelial cells. Cancer Res 65(1):148–156PubMed
208.
go back to reference Kalluri R (2002) Discovery of type IV collagen non-collagenous domains as novel integrin ligands and endogenous inhibitors of angiogenesis. Cold Spring Harb Symp Quant Biol 67:255–266PubMedCrossRef Kalluri R (2002) Discovery of type IV collagen non-collagenous domains as novel integrin ligands and endogenous inhibitors of angiogenesis. Cold Spring Harb Symp Quant Biol 67:255–266PubMedCrossRef
209.
go back to reference Schiemann WP, Blobe GC, Kalume DE et al (2002) Context-specific effects of fibulin-5 (DANCE/EVEC) on cell proliferation, motility, and invasion. Fibulin-5 is induced by transforming growth factor-beta and affects protein kinase cascades. J Biol Chem 277(30):27367–27377 Schiemann WP, Blobe GC, Kalume DE et al (2002) Context-specific effects of fibulin-5 (DANCE/EVEC) on cell proliferation, motility, and invasion. Fibulin-5 is induced by transforming growth factor-beta and affects protein kinase cascades. J Biol Chem 277(30):27367–27377
210.
go back to reference Greenwood JA, Pallero MA, Theibert AB et al (1998) Thrombospondin signaling of focal adhesion disassembly requires activation of phosphoinositide 3-kinase. J Biol Chem 273(3):1755–1763PubMedCrossRef Greenwood JA, Pallero MA, Theibert AB et al (1998) Thrombospondin signaling of focal adhesion disassembly requires activation of phosphoinositide 3-kinase. J Biol Chem 273(3):1755–1763PubMedCrossRef
211.
go back to reference Orr AW, Pallero MA, Murphy-Ullrich JE (2002) Thrombospondin stimulates focal adhesion disassembly through Gi- and phosphoinositide 3-kinase-dependent ERK activation. J Biol Chem 277(23):20453–20460PubMedCrossRef Orr AW, Pallero MA, Murphy-Ullrich JE (2002) Thrombospondin stimulates focal adhesion disassembly through Gi- and phosphoinositide 3-kinase-dependent ERK activation. J Biol Chem 277(23):20453–20460PubMedCrossRef
212.
go back to reference Lopes N, Gregg D, Vasudevan S et al (2003) Thrombospondin 2 regulates cell proliferation induced by Rac1 redox-dependent signaling. Mol Cell Biol 23(15):5401–5408PubMedCrossRef Lopes N, Gregg D, Vasudevan S et al (2003) Thrombospondin 2 regulates cell proliferation induced by Rac1 redox-dependent signaling. Mol Cell Biol 23(15):5401–5408PubMedCrossRef
213.
go back to reference Sudhakar A, Sugimoto H, Yang C et al (2003) Human tumstatin and human endostatin exhibit distinct antiangiogenic activities mediated by alpha v beta 3 and alpha 5 beta 1 integrins. Proc Natl Acad Sci USA 100(8):4766–4771PubMedCrossRef Sudhakar A, Sugimoto H, Yang C et al (2003) Human tumstatin and human endostatin exhibit distinct antiangiogenic activities mediated by alpha v beta 3 and alpha 5 beta 1 integrins. Proc Natl Acad Sci USA 100(8):4766–4771PubMedCrossRef
214.
go back to reference Leali D, Alessi P, Coltrini D et al (2009) Fibroblast growth factor-2 antagonist and antiangiogenic activity of long-pentraxin 3-derived synthetic peptides. Curr Pharm Des 15(30):3577–3589PubMedCrossRef Leali D, Alessi P, Coltrini D et al (2009) Fibroblast growth factor-2 antagonist and antiangiogenic activity of long-pentraxin 3-derived synthetic peptides. Curr Pharm Des 15(30):3577–3589PubMedCrossRef
215.
go back to reference Cai J, Jiang WG, Grant MB et al (2006) Pigment epithelium-derived factor inhibits angiogenesis via regulated intracellular proteolysis of vascular endothelial growth factor receptor 1. J Biol Chem 281(6):3604–3613PubMedCrossRef Cai J, Jiang WG, Grant MB et al (2006) Pigment epithelium-derived factor inhibits angiogenesis via regulated intracellular proteolysis of vascular endothelial growth factor receptor 1. J Biol Chem 281(6):3604–3613PubMedCrossRef
216.
go back to reference Yamagishi S, Amano S, Inagaki Y et al (2003) Pigment epithelium-derived factor inhibits leptin-induced angiogenesis by suppressing vascular endothelial growth factor gene expression through anti-oxidative properties. Microvasc Res 65(3):186–190PubMedCrossRef Yamagishi S, Amano S, Inagaki Y et al (2003) Pigment epithelium-derived factor inhibits leptin-induced angiogenesis by suppressing vascular endothelial growth factor gene expression through anti-oxidative properties. Microvasc Res 65(3):186–190PubMedCrossRef
217.
go back to reference Liu W, Wu Z, Guan M et al (2009) cDNA microarray analysis of pigment epithelium-derived factor-regulated gene expression profile in prostate carcinoma cells. Int J Urol 16(3):323–328PubMedCrossRef Liu W, Wu Z, Guan M et al (2009) cDNA microarray analysis of pigment epithelium-derived factor-regulated gene expression profile in prostate carcinoma cells. Int J Urol 16(3):323–328PubMedCrossRef
218.
go back to reference Chen YH, Wu HL, Chen CK et al (2003) Angiostatin antagonizes the action of VEGF-A in human endothelial cells via two distinct pathways. Biochem Biophys Res Commun 310(3):804–810PubMedCrossRef Chen YH, Wu HL, Chen CK et al (2003) Angiostatin antagonizes the action of VEGF-A in human endothelial cells via two distinct pathways. Biochem Biophys Res Commun 310(3):804–810PubMedCrossRef
219.
go back to reference Bae JS, Rezaie AR (2009) Mutagenesis studies toward understanding the intracellular signaling mechanism of antithrombin. J Thromb Haemost 7(5):803–810PubMedCrossRef Bae JS, Rezaie AR (2009) Mutagenesis studies toward understanding the intracellular signaling mechanism of antithrombin. J Thromb Haemost 7(5):803–810PubMedCrossRef
220.
go back to reference Jouan V, Canron X, Alemany M et al (1999) Inhibition of in vitro angiogenesis by platelet factor-4-derived peptides and mechanism of action. Blood 94(3):984–993PubMed Jouan V, Canron X, Alemany M et al (1999) Inhibition of in vitro angiogenesis by platelet factor-4-derived peptides and mechanism of action. Blood 94(3):984–993PubMed
221.
go back to reference Brooks PC, Silletti S, von Schalscha TL et al (1998) Disruption of angiogenesis by PEX, a noncatalytic metalloproteinase fragment with integrin binding activity. Cell 92(3):391–400PubMedCrossRef Brooks PC, Silletti S, von Schalscha TL et al (1998) Disruption of angiogenesis by PEX, a noncatalytic metalloproteinase fragment with integrin binding activity. Cell 92(3):391–400PubMedCrossRef
222.
go back to reference Moses MA, Wiederschain D, Wu I et al (1999) Troponin I is present in human cartilage and inhibits angiogenesis. Proc Natl Acad Sci USA 96(6):2645–2650PubMedCrossRef Moses MA, Wiederschain D, Wu I et al (1999) Troponin I is present in human cartilage and inhibits angiogenesis. Proc Natl Acad Sci USA 96(6):2645–2650PubMedCrossRef
223.
go back to reference Feldman L, Rouleau C (2002) Troponin I inhibits capillary endothelial cell proliferation by interaction with the cell’s bFGF receptor. Microvasc Res 63(1):41–49PubMedCrossRef Feldman L, Rouleau C (2002) Troponin I inhibits capillary endothelial cell proliferation by interaction with the cell’s bFGF receptor. Microvasc Res 63(1):41–49PubMedCrossRef
224.
go back to reference Blois A, Srebro B, Mandala M et al (2006) The chromogranin A peptide vasostatin-I inhibits gap formation and signal transduction mediated by inflammatory agents in cultured bovine pulmonary and coronary arterial endothelial cells. Regul Pept 135(1–2):78–84PubMedCrossRef Blois A, Srebro B, Mandala M et al (2006) The chromogranin A peptide vasostatin-I inhibits gap formation and signal transduction mediated by inflammatory agents in cultured bovine pulmonary and coronary arterial endothelial cells. Regul Pept 135(1–2):78–84PubMedCrossRef
225.
go back to reference Yang CR, Hsieh SL, Teng CM et al (2004) Soluble decoy receptor 3 induces angiogenesis by neutralization of TL1A, a cytokine belonging to tumor necrosis factor superfamily and exhibiting angiostatic action. Cancer Res 64(3):1122–1129PubMedCrossRef Yang CR, Hsieh SL, Teng CM et al (2004) Soluble decoy receptor 3 induces angiogenesis by neutralization of TL1A, a cytokine belonging to tumor necrosis factor superfamily and exhibiting angiostatic action. Cancer Res 64(3):1122–1129PubMedCrossRef
226.
go back to reference Wen L, Zhuang L, Luo X et al (2003) TL1A-induced NF-kappaB activation and c-IAP2 production prevent DR3-mediated apoptosis in TF-1 cells. J Biol Chem 278(40):39251–39258PubMedCrossRef Wen L, Zhuang L, Luo X et al (2003) TL1A-induced NF-kappaB activation and c-IAP2 production prevent DR3-mediated apoptosis in TF-1 cells. J Biol Chem 278(40):39251–39258PubMedCrossRef
227.
go back to reference Hou W, Medynski D, Wu S et al (2005) VEGI-192, a new isoform of TNFSF15, specifically eliminates tumor vascular endothelial cells and suppresses tumor growth. Clin Cancer Res 11(15):5595–5602PubMedCrossRef Hou W, Medynski D, Wu S et al (2005) VEGI-192, a new isoform of TNFSF15, specifically eliminates tumor vascular endothelial cells and suppresses tumor growth. Clin Cancer Res 11(15):5595–5602PubMedCrossRef
228.
go back to reference Watanabe K, Hasegawa Y, Yamashita H et al (2004) Vasohibin as an endothelium-derived negative feedback regulator of angiogenesis. J Clin Invest 114(7):898–907PubMed Watanabe K, Hasegawa Y, Yamashita H et al (2004) Vasohibin as an endothelium-derived negative feedback regulator of angiogenesis. J Clin Invest 114(7):898–907PubMed
229.
go back to reference Otani A, Slike BM, Dorrell MI et al (2002) A fragment of human TrpRS as a potent antagonist of ocular angiogenesis. Proc Natl Acad Sci USA 99(1):178–183PubMedCrossRef Otani A, Slike BM, Dorrell MI et al (2002) A fragment of human TrpRS as a potent antagonist of ocular angiogenesis. Proc Natl Acad Sci USA 99(1):178–183PubMedCrossRef
230.
go back to reference Tzima E, Reader JS, Irani-Tehrani M et al (2005) VE-cadherin links tRNA synthetase cytokine to anti-angiogenic function. J Biol Chem 280(4):2405–2408PubMedCrossRef Tzima E, Reader JS, Irani-Tehrani M et al (2005) VE-cadherin links tRNA synthetase cytokine to anti-angiogenic function. J Biol Chem 280(4):2405–2408PubMedCrossRef
231.
go back to reference Tong Z, Kunnumakkara AB, Wang H et al (2008) Neutrophil gelatinase-associated lipocalin: a novel suppressor of invasion and angiogenesis in pancreatic cancer. Cancer Res 68(15):6100–6108PubMedCrossRef Tong Z, Kunnumakkara AB, Wang H et al (2008) Neutrophil gelatinase-associated lipocalin: a novel suppressor of invasion and angiogenesis in pancreatic cancer. Cancer Res 68(15):6100–6108PubMedCrossRef
232.
go back to reference Tsuruoka N, Sugiyama M, Tawaragi Y et al (1988) Inhibition of in vitro angiogenesis by lymphotoxin and interferon-gamma. Biochem Biophys Res Commun 155(1):429–435PubMedCrossRef Tsuruoka N, Sugiyama M, Tawaragi Y et al (1988) Inhibition of in vitro angiogenesis by lymphotoxin and interferon-gamma. Biochem Biophys Res Commun 155(1):429–435PubMedCrossRef
233.
go back to reference Strieter RM, Kunkel SL, Arenberg DA et al (1995) Interferon gamma-inducible protein 10 (IP-10), a member of the C-X-C chemokine family, is an inhibitor of angiogenesis. Biochem Biophys Res Commun 210(1):51–57PubMedCrossRef Strieter RM, Kunkel SL, Arenberg DA et al (1995) Interferon gamma-inducible protein 10 (IP-10), a member of the C-X-C chemokine family, is an inhibitor of angiogenesis. Biochem Biophys Res Commun 210(1):51–57PubMedCrossRef
234.
go back to reference Koike F, Satoh J, Miyake S et al (2003) Microarray analysis identifies interferon beta-regulated genes in multiple sclerosis. J Neuroimmunol 139(1–2):109–118PubMedCrossRef Koike F, Satoh J, Miyake S et al (2003) Microarray analysis identifies interferon beta-regulated genes in multiple sclerosis. J Neuroimmunol 139(1–2):109–118PubMedCrossRef
235.
go back to reference Huang T, Tu K, Shyr Y et al (2008) The prediction of interferon treatment effects based on time series microarray gene expression profiles. J Transl Med 6:44PubMedCrossRef Huang T, Tu K, Shyr Y et al (2008) The prediction of interferon treatment effects based on time series microarray gene expression profiles. J Transl Med 6:44PubMedCrossRef
236.
go back to reference Chen Y, Antoniou E, Liu Z et al (2007) A microarray analysis for genes regulated by interferon-tau in ovine luminal epithelial cells. Reproduction 134(1):123–135PubMedCrossRef Chen Y, Antoniou E, Liu Z et al (2007) A microarray analysis for genes regulated by interferon-tau in ovine luminal epithelial cells. Reproduction 134(1):123–135PubMedCrossRef
237.
go back to reference Zou W, Kim JH, Handidu A et al (2007) Microarray analysis reveals that Type I interferon strongly increases the expression of immune-response related genes in Ubp43 (Usp18) deficient macrophages. Biochem Biophys Res Commun 356(1):193–199PubMedCrossRef Zou W, Kim JH, Handidu A et al (2007) Microarray analysis reveals that Type I interferon strongly increases the expression of immune-response related genes in Ubp43 (Usp18) deficient macrophages. Biochem Biophys Res Commun 356(1):193–199PubMedCrossRef
238.
go back to reference Crow MK, Kirou KA, Wohlgemuth J (2003) Microarray analysis of interferon-regulated genes in SLE. Autoimmunity 36(8):481–490PubMedCrossRef Crow MK, Kirou KA, Wohlgemuth J (2003) Microarray analysis of interferon-regulated genes in SLE. Autoimmunity 36(8):481–490PubMedCrossRef
239.
go back to reference Cozzolino F, Torcia M, Aldinucci D et al (1990) Interleukin 1 is an autocrine regulator of human endothelial cell growth. Proc Natl Acad Sci USA 87(17):6487–6491PubMedCrossRef Cozzolino F, Torcia M, Aldinucci D et al (1990) Interleukin 1 is an autocrine regulator of human endothelial cell growth. Proc Natl Acad Sci USA 87(17):6487–6491PubMedCrossRef
240.
go back to reference Tamura T, Nakanishi T, Kimura Y et al (1996) Nitric oxide mediates interleukin-1-induced matrix degradation and basic fibroblast growth factor release in cultured rabbit articular chondrocytes: a possible mechanism of pathological neovascularization in arthritis. Endocrinology 137(9):3729–3737PubMedCrossRef Tamura T, Nakanishi T, Kimura Y et al (1996) Nitric oxide mediates interleukin-1-induced matrix degradation and basic fibroblast growth factor release in cultured rabbit articular chondrocytes: a possible mechanism of pathological neovascularization in arthritis. Endocrinology 137(9):3729–3737PubMedCrossRef
241.
go back to reference Williams MR, Kataoka N, Sakurai Y et al (2008) Gene expression of endothelial cells due to interleukin-1 beta stimulation and neutrophil transmigration. Endothelium 15(1):73–165PubMedCrossRef Williams MR, Kataoka N, Sakurai Y et al (2008) Gene expression of endothelial cells due to interleukin-1 beta stimulation and neutrophil transmigration. Endothelium 15(1):73–165PubMedCrossRef
242.
go back to reference Zhao B, Stavchansky SA, Bowden RA et al (2003) Effect of interleukin-1beta and tumor necrosis factor-alpha on gene expression in human endothelial cells. Am J Physiol Cell Physiol 284(6):C1577–C1583PubMed Zhao B, Stavchansky SA, Bowden RA et al (2003) Effect of interleukin-1beta and tumor necrosis factor-alpha on gene expression in human endothelial cells. Am J Physiol Cell Physiol 284(6):C1577–C1583PubMed
243.
go back to reference Elaraj DM, Weinreich DM, Varghese S et al (2006) The role of interleukin 1 in growth and metastasis of human cancer xenografts. Clin Cancer Res 12(4):1088–1096PubMedCrossRef Elaraj DM, Weinreich DM, Varghese S et al (2006) The role of interleukin 1 in growth and metastasis of human cancer xenografts. Clin Cancer Res 12(4):1088–1096PubMedCrossRef
244.
go back to reference Shi J, Schmitt-Talbot E, DiMattia DA et al (2004) The differential effects of IL-1 and TNF-alpha on proinflammatory cytokine and matrix metalloproteinase expression in human chondrosarcoma cells. Inflamm Res 53(8):377–389PubMedCrossRef Shi J, Schmitt-Talbot E, DiMattia DA et al (2004) The differential effects of IL-1 and TNF-alpha on proinflammatory cytokine and matrix metalloproteinase expression in human chondrosarcoma cells. Inflamm Res 53(8):377–389PubMedCrossRef
245.
go back to reference Berchtold LA, Larsen CM, Vaag A et al (2009) IL-1 receptor antagonism and muscle gene expression in patients with type 2 diabetes. Eur Cytokine Netw 20(2):81–87PubMed Berchtold LA, Larsen CM, Vaag A et al (2009) IL-1 receptor antagonism and muscle gene expression in patients with type 2 diabetes. Eur Cytokine Netw 20(2):81–87PubMed
246.
go back to reference Ching S, Zhang H, Chen Q et al (2007) Differential expression of extracellular matrix and adhesion molecule genes in the brain of juvenile versus adult mice in responses to intracerebroventricular administration of IL-1. Neuroimmunomodulation 14(1):46–56PubMedCrossRef Ching S, Zhang H, Chen Q et al (2007) Differential expression of extracellular matrix and adhesion molecule genes in the brain of juvenile versus adult mice in responses to intracerebroventricular administration of IL-1. Neuroimmunomodulation 14(1):46–56PubMedCrossRef
247.
go back to reference Volpert OV, Fong T, Koch AE et al (1998) Inhibition of angiogenesis by interleukin 4. J Exp Med 188(6):1039–1046PubMedCrossRef Volpert OV, Fong T, Koch AE et al (1998) Inhibition of angiogenesis by interleukin 4. J Exp Med 188(6):1039–1046PubMedCrossRef
248.
go back to reference Schnyder B, Lugli S, Feng N et al (1996) Interleukin-4 (IL-4) and IL-13 bind to a shared heterodimeric complex on endothelial cells mediating vascular cell adhesion molecule-1 induction in the absence of the common gamma chain. Blood 87(10):4286–4295PubMed Schnyder B, Lugli S, Feng N et al (1996) Interleukin-4 (IL-4) and IL-13 bind to a shared heterodimeric complex on endothelial cells mediating vascular cell adhesion molecule-1 induction in the absence of the common gamma chain. Blood 87(10):4286–4295PubMed
249.
go back to reference Matsumoto K, Ohi H, Kanmatsuse K (1999) Interleukin-4 cooperates with interleukin-10 to inhibit vascular permeability factor release by peripheral blood mononuclear cells from patients with minimal-change nephrotic syndrome. Am J Nephrol 19(1):21–27PubMedCrossRef Matsumoto K, Ohi H, Kanmatsuse K (1999) Interleukin-4 cooperates with interleukin-10 to inhibit vascular permeability factor release by peripheral blood mononuclear cells from patients with minimal-change nephrotic syndrome. Am J Nephrol 19(1):21–27PubMedCrossRef
250.
go back to reference Chaitidis P, O’Donnell V, Kuban RJ et al (2005) Gene expression alterations of human peripheral blood monocytes induced by medium-term treatment with the TH2-cytokines interleukin-4 and -13. Cytokine 30(6):366–377PubMedCrossRef Chaitidis P, O’Donnell V, Kuban RJ et al (2005) Gene expression alterations of human peripheral blood monocytes induced by medium-term treatment with the TH2-cytokines interleukin-4 and -13. Cytokine 30(6):366–377PubMedCrossRef
251.
go back to reference Lee YW, Eum SY, Chen KC et al (2004) Gene expression profile in interleukin-4-stimulated human vascular endothelial cells. Mol Med 10(1–6):19–27PubMed Lee YW, Eum SY, Chen KC et al (2004) Gene expression profile in interleukin-4-stimulated human vascular endothelial cells. Mol Med 10(1–6):19–27PubMed
252.
go back to reference Coughlin CM, Salhany KE, Gee MS et al (1998) Tumor cell responses to IFNgamma affect tumorigenicity and response to IL-12 therapy and antiangiogenesis. Immunity 9(1):25–34PubMedCrossRef Coughlin CM, Salhany KE, Gee MS et al (1998) Tumor cell responses to IFNgamma affect tumorigenicity and response to IL-12 therapy and antiangiogenesis. Immunity 9(1):25–34PubMedCrossRef
253.
go back to reference Dias S, Boyd R, Balkwill F (1998) IL-12 regulates VEGF and MMPs in a murine breast cancer model. Int J Cancer 78(3):361–365PubMedCrossRef Dias S, Boyd R, Balkwill F (1998) IL-12 regulates VEGF and MMPs in a murine breast cancer model. Int J Cancer 78(3):361–365PubMedCrossRef
254.
go back to reference Renneson J, Dutta B, Goriely S et al (2009) IL-12 and type I IFN response of neonatal myeloid DC to human cytomegalovirus infection. Eur J Immunol 39(10):2789–2799PubMedCrossRef Renneson J, Dutta B, Goriely S et al (2009) IL-12 and type I IFN response of neonatal myeloid DC to human cytomegalovirus infection. Eur J Immunol 39(10):2789–2799PubMedCrossRef
255.
go back to reference Shi Y, Zou M, Baitei EY et al (2008) Cannabinoid 2 receptor induction by IL-12 and its potential as a therapeutic target for the treatment of anaplastic thyroid carcinoma. Cancer Gene Ther 15(2):101–107PubMedCrossRef Shi Y, Zou M, Baitei EY et al (2008) Cannabinoid 2 receptor induction by IL-12 and its potential as a therapeutic target for the treatment of anaplastic thyroid carcinoma. Cancer Gene Ther 15(2):101–107PubMedCrossRef
256.
go back to reference Hoey T, Zhang S, Schmidt N et al (2003) Distinct requirements for the naturally occurring splice forms Stat4alpha and Stat4beta in IL-12 responses. EMBO J 22(16):4237–4248PubMedCrossRef Hoey T, Zhang S, Schmidt N et al (2003) Distinct requirements for the naturally occurring splice forms Stat4alpha and Stat4beta in IL-12 responses. EMBO J 22(16):4237–4248PubMedCrossRef
257.
go back to reference Hodge DL, Schill WB, Wang JM et al (2002) IL-2 and IL-12 alter NK cell responsiveness to IFN-gamma-inducible protein 10 by down-regulating CXCR3 expression. J Immunol 168(12):6090–6098PubMed Hodge DL, Schill WB, Wang JM et al (2002) IL-2 and IL-12 alter NK cell responsiveness to IFN-gamma-inducible protein 10 by down-regulating CXCR3 expression. J Immunol 168(12):6090–6098PubMed
258.
go back to reference Cao R, Farnebo J, Kurimoto M et al (1999) Interleukin-18 acts as an angiogenesis and tumor suppressor. FASEB J 13(15):2195–2202PubMed Cao R, Farnebo J, Kurimoto M et al (1999) Interleukin-18 acts as an angiogenesis and tumor suppressor. FASEB J 13(15):2195–2202PubMed
259.
go back to reference Kim J, Kim C, Kim TS et al (2006) IL-18 enhances thrombospondin-1 production in human gastric cancer via JNK pathway. Biochem Biophys Res Commun 344(4):1284–1289PubMedCrossRef Kim J, Kim C, Kim TS et al (2006) IL-18 enhances thrombospondin-1 production in human gastric cancer via JNK pathway. Biochem Biophys Res Commun 344(4):1284–1289PubMedCrossRef
260.
go back to reference Coma G, Pena R, Blanco J et al (2006) Treatment of monocytes with interleukin (IL)-12 plus IL-18 stimulates survival, differentiation and the production of CXC chemokine ligands (CXCL)8, CXCL9 and CXCL10. Clin Exp Immunol 145(3):535–544PubMedCrossRef Coma G, Pena R, Blanco J et al (2006) Treatment of monocytes with interleukin (IL)-12 plus IL-18 stimulates survival, differentiation and the production of CXC chemokine ligands (CXCL)8, CXCL9 and CXCL10. Clin Exp Immunol 145(3):535–544PubMedCrossRef
261.
go back to reference Wiener Z, Pocza P, Racz M et al (2008) IL-18 induces a marked gene expression profile change and increased Ccl1 (I-309) production in mouse mucosal mast cell homologs. Int Immunol 20(12):1565–1573PubMedCrossRef Wiener Z, Pocza P, Racz M et al (2008) IL-18 induces a marked gene expression profile change and increased Ccl1 (I-309) production in mouse mucosal mast cell homologs. Int Immunol 20(12):1565–1573PubMedCrossRef
262.
go back to reference Seo M, Park M, Yook Y et al (2008) IL-18 gene expression pattern in exogenously treated AML cells. BMB Rep 41(6):461–465PubMed Seo M, Park M, Yook Y et al (2008) IL-18 gene expression pattern in exogenously treated AML cells. BMB Rep 41(6):461–465PubMed
263.
go back to reference Saha S, Gonzalez J, Rosenfeld G et al (2009) Prolactin alters the mechanisms of B cell tolerance induction. Arthritis Rheum 60(6):1743–1752PubMedCrossRef Saha S, Gonzalez J, Rosenfeld G et al (2009) Prolactin alters the mechanisms of B cell tolerance induction. Arthritis Rheum 60(6):1743–1752PubMedCrossRef
264.
go back to reference Charoenphandhu N, Wongdee K, Teerapornpuntakit J et al (2008) Transcriptome responses of duodenal epithelial cells to prolactin in pituitary-grafted rats. Mol Cell Endocrinol 296(1–2):41–52PubMedCrossRef Charoenphandhu N, Wongdee K, Teerapornpuntakit J et al (2008) Transcriptome responses of duodenal epithelial cells to prolactin in pituitary-grafted rats. Mol Cell Endocrinol 296(1–2):41–52PubMedCrossRef
265.
go back to reference Tomblyn S, Langenheim JF, Jacquemart IC et al (2005) The role of human prolactin and its antagonist, G129R, in mammary gland development and DMBA-initiated tumorigenesis in transgenic mice. Int J Oncol 27(5):1381–1389PubMed Tomblyn S, Langenheim JF, Jacquemart IC et al (2005) The role of human prolactin and its antagonist, G129R, in mammary gland development and DMBA-initiated tumorigenesis in transgenic mice. Int J Oncol 27(5):1381–1389PubMed
266.
go back to reference Gass S, Harris J, Ormandy C et al (2003) Using gene expression arrays to elucidate transcriptional profiles underlying prolactin function. J Mammary Gland Biol Neoplasia 8(3):269–285PubMedCrossRef Gass S, Harris J, Ormandy C et al (2003) Using gene expression arrays to elucidate transcriptional profiles underlying prolactin function. J Mammary Gland Biol Neoplasia 8(3):269–285PubMedCrossRef
267.
go back to reference Dillner K, Kindblom J, Flores-Morales A et al (2003) Gene expression analysis of prostate hyperplasia in mice overexpressing the prolactin gene specifically in the prostate. Endocrinology 144(11):4955–4966PubMedCrossRef Dillner K, Kindblom J, Flores-Morales A et al (2003) Gene expression analysis of prostate hyperplasia in mice overexpressing the prolactin gene specifically in the prostate. Endocrinology 144(11):4955–4966PubMedCrossRef
268.
go back to reference Dillner K, Kindblom J, Flores-Morales A et al (2002) Molecular characterization of prostate hyperplasia in prolactin-transgenic mice by using cDNA representational difference analysis. Prostate 52(2):139–149PubMedCrossRef Dillner K, Kindblom J, Flores-Morales A et al (2002) Molecular characterization of prostate hyperplasia in prolactin-transgenic mice by using cDNA representational difference analysis. Prostate 52(2):139–149PubMedCrossRef
269.
go back to reference Hou Z, Bailey JP, Vomachka AJ et al (2000) Glycosylation-dependent cell adhesion molecule 1 (GlyCAM 1) is induced by prolactin and suppressed by progesterone in mammary epithelium. Endocrinology 141(11):4278–4283PubMedCrossRef Hou Z, Bailey JP, Vomachka AJ et al (2000) Glycosylation-dependent cell adhesion molecule 1 (GlyCAM 1) is induced by prolactin and suppressed by progesterone in mammary epithelium. Endocrinology 141(11):4278–4283PubMedCrossRef
270.
go back to reference Quan H, Xu Y, Lou L (2008) p38 MAPK, but not ERK1/2, is critically involved in the cytotoxicity of the novel vascular disrupting agent combretastatin A4. Int J Cancer 122(8):1730–1737PubMedCrossRef Quan H, Xu Y, Lou L (2008) p38 MAPK, but not ERK1/2, is critically involved in the cytotoxicity of the novel vascular disrupting agent combretastatin A4. Int J Cancer 122(8):1730–1737PubMedCrossRef
271.
go back to reference Wang YQ, Luk JM, Chu AC et al (2006) TNP-470 blockage of VEGF synthesis is dependent on MAPK/COX-2 signaling pathway in PDGF-BB-activated hepatic stellate cells. Biochem Biophys Res Commun 341(1):239–244PubMedCrossRef Wang YQ, Luk JM, Chu AC et al (2006) TNP-470 blockage of VEGF synthesis is dependent on MAPK/COX-2 signaling pathway in PDGF-BB-activated hepatic stellate cells. Biochem Biophys Res Commun 341(1):239–244PubMedCrossRef
272.
go back to reference Chen GJ, Weylie B, Hu C et al (2007) FGFR1/PI3 K/AKT signaling pathway is a novel target for antiangiogenic effects of the cancer drug fumagillin (TNP-470). J Cell Biochem 101(6):1492–1504PubMedCrossRef Chen GJ, Weylie B, Hu C et al (2007) FGFR1/PI3 K/AKT signaling pathway is a novel target for antiangiogenic effects of the cancer drug fumagillin (TNP-470). J Cell Biochem 101(6):1492–1504PubMedCrossRef
273.
go back to reference Koseki Y, Zava DT, Chamness GC et al (1977) Estrogen receptor translocation and replenishment by the antiestrogen tamoxifen. Endocrinology 101(4):1104–1110PubMedCrossRef Koseki Y, Zava DT, Chamness GC et al (1977) Estrogen receptor translocation and replenishment by the antiestrogen tamoxifen. Endocrinology 101(4):1104–1110PubMedCrossRef
274.
go back to reference Inai T, Mancuso M, Hashizume H et al (2004) Inhibition of vascular endothelial growth factor (VEGF) signaling in cancer causes loss of endothelial fenestrations, regression of tumor vessels, and appearance of basement membrane ghosts. Am J Pathol 165(1):35–52PubMed Inai T, Mancuso M, Hashizume H et al (2004) Inhibition of vascular endothelial growth factor (VEGF) signaling in cancer causes loss of endothelial fenestrations, regression of tumor vessels, and appearance of basement membrane ghosts. Am J Pathol 165(1):35–52PubMed
275.
go back to reference Nghiemphu PL, Liu W, Lee Y et al (2009) Bevacizumab and chemotherapy for recurrent glioblastoma: a single-institution experience. Neurology 72(14):1217–1222PubMedCrossRef Nghiemphu PL, Liu W, Lee Y et al (2009) Bevacizumab and chemotherapy for recurrent glioblastoma: a single-institution experience. Neurology 72(14):1217–1222PubMedCrossRef
276.
go back to reference Maier AK, Kociok N, Zahn G et al (2007) Modulation of hypoxia-induced neovascularization by JSM6427, an integrin alpha5beta1 inhibiting molecule. Curr Eye Res 32(9):801–812PubMedCrossRef Maier AK, Kociok N, Zahn G et al (2007) Modulation of hypoxia-induced neovascularization by JSM6427, an integrin alpha5beta1 inhibiting molecule. Curr Eye Res 32(9):801–812PubMedCrossRef
277.
go back to reference Strumberg D (2005) Preclinical and clinical development of the oral multikinase inhibitor sorafenib in cancer treatment. Drugs Today (Barc) 41(12):773–784CrossRef Strumberg D (2005) Preclinical and clinical development of the oral multikinase inhibitor sorafenib in cancer treatment. Drugs Today (Barc) 41(12):773–784CrossRef
278.
go back to reference Gragoudas ES, Adamis AP, Cunningham ET Jr et al (2004) Pegaptanib for neovascular age-related macular degeneration. N Engl J Med 351(27):2805–2816PubMedCrossRef Gragoudas ES, Adamis AP, Cunningham ET Jr et al (2004) Pegaptanib for neovascular age-related macular degeneration. N Engl J Med 351(27):2805–2816PubMedCrossRef
279.
go back to reference Banerjee S, Zvelebil M, Furet P et al (2009) The vascular endothelial growth factor receptor inhibitor PTK787/ZK222584 inhibits aromatase. Cancer Res 69(11):4716–4723PubMedCrossRef Banerjee S, Zvelebil M, Furet P et al (2009) The vascular endothelial growth factor receptor inhibitor PTK787/ZK222584 inhibits aromatase. Cancer Res 69(11):4716–4723PubMedCrossRef
280.
go back to reference Rosenfeld PJ, Brown DM, Heier JS et al (2006) Ranibizumab for neovascular age-related macular degeneration. N Engl J Med 355(14):1419–1431PubMedCrossRef Rosenfeld PJ, Brown DM, Heier JS et al (2006) Ranibizumab for neovascular age-related macular degeneration. N Engl J Med 355(14):1419–1431PubMedCrossRef
281.
go back to reference Hosoi H, Dilling MB, Shikata T et al (1999) Rapamycin causes poorly reversible inhibition of mTOR and induces p53-independent apoptosis in human rhabdomyosarcoma cells. Cancer Res 59(4):886–894PubMed Hosoi H, Dilling MB, Shikata T et al (1999) Rapamycin causes poorly reversible inhibition of mTOR and induces p53-independent apoptosis in human rhabdomyosarcoma cells. Cancer Res 59(4):886–894PubMed
282.
go back to reference Preiss T, Baron-Benhamou J, Ansorge W et al (2003) Homodirectional changes in transcriptome composition and mRNA translation induced by rapamycin and heat shock. Nat Struct Biol 10(12):1039–1047PubMedCrossRef Preiss T, Baron-Benhamou J, Ansorge W et al (2003) Homodirectional changes in transcriptome composition and mRNA translation induced by rapamycin and heat shock. Nat Struct Biol 10(12):1039–1047PubMedCrossRef
283.
go back to reference Palanki MS, Akiyama H, Campochiaro P et al (2008) Development of prodrug 4-chloro-3-(5-methyl-3-{[4-(2-pyrrolidin-1-ylethoxy)phenyl]amino}-1, 2, 4-be nzotriazin-7-yl)phenyl benzoate (TG100801): a topically administered therapeutic candidate in clinical trials for the treatment of age-related macular degeneration. J Med Chem 51(6):1546–1559PubMedCrossRef Palanki MS, Akiyama H, Campochiaro P et al (2008) Development of prodrug 4-chloro-3-(5-methyl-3-{[4-(2-pyrrolidin-1-ylethoxy)phenyl]amino}-1, 2, 4-be nzotriazin-7-yl)phenyl benzoate (TG100801): a topically administered therapeutic candidate in clinical trials for the treatment of age-related macular degeneration. J Med Chem 51(6):1546–1559PubMedCrossRef
284.
go back to reference Fabbrini M, Trachsel E, Soldani P et al (2006) Selective occlusion of tumor blood vessels by targeted delivery of an antibody-photosensitizer conjugate. Int J Cancer 118(7):1805–1813PubMedCrossRef Fabbrini M, Trachsel E, Soldani P et al (2006) Selective occlusion of tumor blood vessels by targeted delivery of an antibody-photosensitizer conjugate. Int J Cancer 118(7):1805–1813PubMedCrossRef
285.
go back to reference Billerey-Larmonier C, Uno JK, Larmonier N et al (2008) Protective effects of dietary curcumin in mouse model of chemically induced colitis are strain dependent. Inflamm Bowel Dis 14(6):780–793PubMedCrossRef Billerey-Larmonier C, Uno JK, Larmonier N et al (2008) Protective effects of dietary curcumin in mouse model of chemically induced colitis are strain dependent. Inflamm Bowel Dis 14(6):780–793PubMedCrossRef
286.
go back to reference Nguyen KT, Shaikh N, Shukla KP et al (2004) Molecular responses of vascular smooth muscle cells and phagocytes to curcumin-eluting bioresorbable stent materials. Biomaterials 25(23):5333–5346PubMedCrossRef Nguyen KT, Shaikh N, Shukla KP et al (2004) Molecular responses of vascular smooth muscle cells and phagocytes to curcumin-eluting bioresorbable stent materials. Biomaterials 25(23):5333–5346PubMedCrossRef
287.
go back to reference Chen HW, Yu SL, Chen JJ et al (2004) Anti-invasive gene expression profile of curcumin in lung adenocarcinoma based on a high throughput microarray analysis. Mol Pharmacol 65(1):99–110PubMedCrossRef Chen HW, Yu SL, Chen JJ et al (2004) Anti-invasive gene expression profile of curcumin in lung adenocarcinoma based on a high throughput microarray analysis. Mol Pharmacol 65(1):99–110PubMedCrossRef
288.
go back to reference Mariadason JM, Corner GA, Augenlicht LH (2000) Genetic reprogramming in pathways of colonic cell maturation induced by short chain fatty acids: comparison with trichostatin A, sulindac, and curcumin and implications for chemoprevention of colon cancer. Cancer Res 60(16):4561–4572PubMed Mariadason JM, Corner GA, Augenlicht LH (2000) Genetic reprogramming in pathways of colonic cell maturation induced by short chain fatty acids: comparison with trichostatin A, sulindac, and curcumin and implications for chemoprevention of colon cancer. Cancer Res 60(16):4561–4572PubMed
289.
go back to reference Papoutsi Z, Kassi E, Chinou I et al (2008) Walnut extract (Juglans regia L.) and its component ellagic acid exhibit anti-inflammatory activity in human aorta endothelial cells and osteoblastic activity in the cell line KS483. Br J Nutr 99(4):715–722 Papoutsi Z, Kassi E, Chinou I et al (2008) Walnut extract (Juglans regia L.) and its component ellagic acid exhibit anti-inflammatory activity in human aorta endothelial cells and osteoblastic activity in the cell line KS483. Br J Nutr 99(4):715–722
290.
go back to reference Fassina G, Vene R, Morini M et al (2004) Mechanisms of inhibition of tumor angiogenesis and vascular tumor growth by epigallocatechin-3-gallate. Clin Cancer Res 10(14):4865–4873PubMedCrossRef Fassina G, Vene R, Morini M et al (2004) Mechanisms of inhibition of tumor angiogenesis and vascular tumor growth by epigallocatechin-3-gallate. Clin Cancer Res 10(14):4865–4873PubMedCrossRef
291.
go back to reference Garbisa S, Sartor L, Biggin S et al (2001) Tumor gelatinases and invasion inhibited by the green tea flavanol epigallocatechin-3-gallate. Cancer 91(4):822–832PubMedCrossRef Garbisa S, Sartor L, Biggin S et al (2001) Tumor gelatinases and invasion inhibited by the green tea flavanol epigallocatechin-3-gallate. Cancer 91(4):822–832PubMedCrossRef
292.
go back to reference Vittal R, Selvanayagam ZE, Sun Y et al (2004) Gene expression changes induced by green tea polyphenol (-)-epigallocatechin-3-gallate in human bronchial epithelial 21BES cells analyzed by DNA microarray. Mol Cancer Ther 3(9):1091–1099PubMed Vittal R, Selvanayagam ZE, Sun Y et al (2004) Gene expression changes induced by green tea polyphenol (-)-epigallocatechin-3-gallate in human bronchial epithelial 21BES cells analyzed by DNA microarray. Mol Cancer Ther 3(9):1091–1099PubMed
293.
go back to reference Weinreb O, Mandel S, Youdim MB (2003) Gene and protein expression profiles of anti- and pro-apoptotic actions of dopamine, R-apomorphine, green tea polyphenol (-)-epigallocatechine-3-gallate, and melatonin. Ann NY Acad Sci 993:351–61 (discussion 87–93) Weinreb O, Mandel S, Youdim MB (2003) Gene and protein expression profiles of anti- and pro-apoptotic actions of dopamine, R-apomorphine, green tea polyphenol (-)-epigallocatechine-3-gallate, and melatonin. Ann NY Acad Sci 993:351–61 (discussion 87–93)
294.
go back to reference Wang SI, Mukhtar H (2002) Gene expression profile in human prostate LNCaP cancer cells by (–) epigallocatechin-3-gallate. Cancer Lett 182(1):43–51PubMedCrossRef Wang SI, Mukhtar H (2002) Gene expression profile in human prostate LNCaP cancer cells by (–) epigallocatechin-3-gallate. Cancer Lett 182(1):43–51PubMedCrossRef
295.
go back to reference Schempp CM, Kiss J, Kirkin V et al (2005) Hyperforin acts as an angiogenesis inhibitor. Planta Med 71(11):999–1004PubMedCrossRef Schempp CM, Kiss J, Kirkin V et al (2005) Hyperforin acts as an angiogenesis inhibitor. Planta Med 71(11):999–1004PubMedCrossRef
296.
go back to reference Martinez-Poveda B, Quesada AR, Medina MA (2005) Hyperforin, a bio-active compound of St. John’s Wort, is a new inhibitor of angiogenesis targeting several key steps of the process. Int J Cancer 117(5):775–780 Martinez-Poveda B, Quesada AR, Medina MA (2005) Hyperforin, a bio-active compound of St. John’s Wort, is a new inhibitor of angiogenesis targeting several key steps of the process. Int J Cancer 117(5):775–780
297.
go back to reference Quiney C, Billard C, Mirshahi P et al (2006) Hyperforin inhibits MMP-9 secretion by B-CLL cells and microtubule formation by endothelial cells. Leukemia 20(4):583–589PubMedCrossRef Quiney C, Billard C, Mirshahi P et al (2006) Hyperforin inhibits MMP-9 secretion by B-CLL cells and microtubule formation by endothelial cells. Leukemia 20(4):583–589PubMedCrossRef
298.
go back to reference Rakshit S, Bagchi J, Mandal L et al (2009) N-acetyl cysteine enhances imatinib-induced apoptosis of Bcr-Abl + cells by endothelial nitric oxide synthase-mediated production of nitric oxide. Apoptosis 14(3):298–308PubMedCrossRef Rakshit S, Bagchi J, Mandal L et al (2009) N-acetyl cysteine enhances imatinib-induced apoptosis of Bcr-Abl + cells by endothelial nitric oxide synthase-mediated production of nitric oxide. Apoptosis 14(3):298–308PubMedCrossRef
299.
go back to reference Yi T, Cho SG, Yi Z et al (2008) Thymoquinone inhibits tumor angiogenesis and tumor growth through suppressing AKT and extracellular signal-regulated kinase signaling pathways. Mol Cancer Ther 7(7):1789–1796PubMedCrossRef Yi T, Cho SG, Yi Z et al (2008) Thymoquinone inhibits tumor angiogenesis and tumor growth through suppressing AKT and extracellular signal-regulated kinase signaling pathways. Mol Cancer Ther 7(7):1789–1796PubMedCrossRef
300.
go back to reference Su SJ, Yeh TM, Chuang WJ et al (2005) The novel targets for anti-angiogenesis of genistein on human cancer cells. Biochem Pharmacol 69(2):307–318PubMedCrossRef Su SJ, Yeh TM, Chuang WJ et al (2005) The novel targets for anti-angiogenesis of genistein on human cancer cells. Biochem Pharmacol 69(2):307–318PubMedCrossRef
301.
go back to reference Wang TT, Sathyamoorthy N, Phang JM (1996) Molecular effects of genistein on estrogen receptor mediated pathways. Carcinogenesis 17(2):271–275PubMedCrossRef Wang TT, Sathyamoorthy N, Phang JM (1996) Molecular effects of genistein on estrogen receptor mediated pathways. Carcinogenesis 17(2):271–275PubMedCrossRef
302.
go back to reference Li Y, Sarkar FH (2002) Down-regulation of invasion and angiogenesis-related genes identified by cDNA microarray analysis of PC3 prostate cancer cells treated with genistein. Cancer Lett 186(2):157–164PubMedCrossRef Li Y, Sarkar FH (2002) Down-regulation of invasion and angiogenesis-related genes identified by cDNA microarray analysis of PC3 prostate cancer cells treated with genistein. Cancer Lett 186(2):157–164PubMedCrossRef
303.
go back to reference Regenbrecht CR, Jung M, Lehrach H et al (2008) The molecular basis of genistein-induced mitotic arrest, exit of self-renewal in embryonal carcinoma, primary cancer cell lines. BMC Med Genomics 1:49PubMedCrossRef Regenbrecht CR, Jung M, Lehrach H et al (2008) The molecular basis of genistein-induced mitotic arrest, exit of self-renewal in embryonal carcinoma, primary cancer cell lines. BMC Med Genomics 1:49PubMedCrossRef
304.
go back to reference Pie JE, Park JH, Park YH et al (2006) Effect of genistein on the expression of bone metabolism genes in ovariectomized mice using a cDNA microarray. J Nutr Biochem 17(3):157–164PubMedCrossRef Pie JE, Park JH, Park YH et al (2006) Effect of genistein on the expression of bone metabolism genes in ovariectomized mice using a cDNA microarray. J Nutr Biochem 17(3):157–164PubMedCrossRef
305.
go back to reference Takahashi Y, Lavigne JA, Hursting SD et al (2004) Using DNA microarray analyses to elucidate the effects of genistein in androgen-responsive prostate cancer cells: identification of novel targets. Mol Carcinog 41(2):108–119PubMedCrossRef Takahashi Y, Lavigne JA, Hursting SD et al (2004) Using DNA microarray analyses to elucidate the effects of genistein in androgen-responsive prostate cancer cells: identification of novel targets. Mol Carcinog 41(2):108–119PubMedCrossRef
306.
go back to reference Adachi T, Ono Y, Koh KB et al (2004) Long-term alteration of gene expression without morphological change in testis after neonatal exposure to genistein in mice: toxicogenomic analysis using cDNA microarray. Food Chem Toxicol 42(3):445–452PubMedCrossRef Adachi T, Ono Y, Koh KB et al (2004) Long-term alteration of gene expression without morphological change in testis after neonatal exposure to genistein in mice: toxicogenomic analysis using cDNA microarray. Food Chem Toxicol 42(3):445–452PubMedCrossRef
307.
go back to reference Chen WF, Huang MH, Tzang CH et al (2003) Inhibitory actions of genistein in human breast cancer (MCF-7) cells. Biochim Biophys Acta 1638(2):187–196PubMed Chen WF, Huang MH, Tzang CH et al (2003) Inhibitory actions of genistein in human breast cancer (MCF-7) cells. Biochim Biophys Acta 1638(2):187–196PubMed
308.
go back to reference Naciff JM, Jump ML, Torontali SM et al (2002) Gene expression profile induced by 17alpha-ethynyl estradiol, bisphenol A, and genistein in the developing female reproductive system of the rat. Toxicol Sci 68(1):184–199PubMedCrossRef Naciff JM, Jump ML, Torontali SM et al (2002) Gene expression profile induced by 17alpha-ethynyl estradiol, bisphenol A, and genistein in the developing female reproductive system of the rat. Toxicol Sci 68(1):184–199PubMedCrossRef
309.
go back to reference Chen CC, Shieh B, Jin YT et al (2001) Microarray profiling of gene expression patterns in bladder tumor cells treated with genistein. J Biomed Sci 8(2):214–222PubMedCrossRef Chen CC, Shieh B, Jin YT et al (2001) Microarray profiling of gene expression patterns in bladder tumor cells treated with genistein. J Biomed Sci 8(2):214–222PubMedCrossRef
310.
go back to reference Kobori M, Masumoto S, Akimoto Y et al (2009) Dietary quercetin alleviates diabetic symptoms and reduces streptozotocin-induced disturbance of hepatic gene expression in mice. Mol Nutr Food Res 53(7):859–868PubMedCrossRef Kobori M, Masumoto S, Akimoto Y et al (2009) Dietary quercetin alleviates diabetic symptoms and reduces streptozotocin-induced disturbance of hepatic gene expression in mice. Mol Nutr Food Res 53(7):859–868PubMedCrossRef
311.
go back to reference Natsume Y, Kadota K, Satsu H et al (2009) Effect of quercetin on the gene expression profile of the mouse intestine. Biosci Biotechnol Biochem 73(3):722–725PubMedCrossRef Natsume Y, Kadota K, Satsu H et al (2009) Effect of quercetin on the gene expression profile of the mouse intestine. Biosci Biotechnol Biochem 73(3):722–725PubMedCrossRef
312.
go back to reference Odbayar TO, Kimura T, Tsushida T et al (2009) Isoenzyme-specific up-regulation of glutathione transferase and aldo-keto reductase mRNA expression by dietary quercetin in rat liver. Mol Cell Biochem 325(1–2):121–130PubMedCrossRef Odbayar TO, Kimura T, Tsushida T et al (2009) Isoenzyme-specific up-regulation of glutathione transferase and aldo-keto reductase mRNA expression by dietary quercetin in rat liver. Mol Cell Biochem 325(1–2):121–130PubMedCrossRef
313.
go back to reference Soundararajan R, Wishart AD, Rupasinghe HP et al (2008) Quercetin 3-glucoside protects neuroblastoma (SH-SY5Y) cells in vitro against oxidative damage by inducing sterol regulatory element-binding protein-2-mediated cholesterol biosynthesis. J Biol Chem 283(4):2231–2245PubMedCrossRef Soundararajan R, Wishart AD, Rupasinghe HP et al (2008) Quercetin 3-glucoside protects neuroblastoma (SH-SY5Y) cells in vitro against oxidative damage by inducing sterol regulatory element-binding protein-2-mediated cholesterol biosynthesis. J Biol Chem 283(4):2231–2245PubMedCrossRef
314.
go back to reference Murtaza I, Marra G, Schlapbach R et al (2006) A preliminary investigation demonstrating the effect of quercetin on the expression of genes related to cell-cycle arrest, apoptosis and xenobiotic metabolism in human CO115 colon-adenocarcinoma cells using DNA microarray. Biotechnol Appl Biochem 45(Pt 1):29–36PubMed Murtaza I, Marra G, Schlapbach R et al (2006) A preliminary investigation demonstrating the effect of quercetin on the expression of genes related to cell-cycle arrest, apoptosis and xenobiotic metabolism in human CO115 colon-adenocarcinoma cells using DNA microarray. Biotechnol Appl Biochem 45(Pt 1):29–36PubMed
315.
go back to reference Whyte L, Huang YY, Torres K et al (2007) Molecular mechanisms of resveratrol action in lung cancer cells using dual protein and microarray analyses. Cancer Res 67(24):12007–12017PubMedCrossRef Whyte L, Huang YY, Torres K et al (2007) Molecular mechanisms of resveratrol action in lung cancer cells using dual protein and microarray analyses. Cancer Res 67(24):12007–12017PubMedCrossRef
316.
go back to reference Golkar L, Ding XZ, Ujiki MB et al (2007) Resveratrol inhibits pancreatic cancer cell proliferation through transcriptional induction of macrophage inhibitory cytokine-1. J Surg Res 138(2):163–169PubMedCrossRef Golkar L, Ding XZ, Ujiki MB et al (2007) Resveratrol inhibits pancreatic cancer cell proliferation through transcriptional induction of macrophage inhibitory cytokine-1. J Surg Res 138(2):163–169PubMedCrossRef
317.
go back to reference Jones SB, DePrimo SE, Whitfield ML et al (2005) Resveratrol-induced gene expression profiles in human prostate cancer cells. Cancer Epidemiol Biomarkers Prev 14(3):596–604PubMedCrossRef Jones SB, DePrimo SE, Whitfield ML et al (2005) Resveratrol-induced gene expression profiles in human prostate cancer cells. Cancer Epidemiol Biomarkers Prev 14(3):596–604PubMedCrossRef
318.
go back to reference Yang SH, Kim JS, Oh TJ et al (2003) Genome-scale analysis of resveratrol-induced gene expression profile in human ovarian cancer cells using a cDNA microarray. Int J Oncol 22(4):741–750PubMed Yang SH, Kim JS, Oh TJ et al (2003) Genome-scale analysis of resveratrol-induced gene expression profile in human ovarian cancer cells using a cDNA microarray. Int J Oncol 22(4):741–750PubMed
319.
go back to reference Narayanan BA, Narayanan NK, Re GG et al (2003) Differential expression of genes induced by resveratrol in LNCaP cells: P53-mediated molecular targets. Int J Cancer 104(2):204–212PubMedCrossRef Narayanan BA, Narayanan NK, Re GG et al (2003) Differential expression of genes induced by resveratrol in LNCaP cells: P53-mediated molecular targets. Int J Cancer 104(2):204–212PubMedCrossRef
Metadata
Title
Functional genomics of endothelial cells treated with anti-angiogenic or angiopreventive drugs
Authors
Adriana Albini
Stefano Indraccolo
Douglas M. Noonan
Ulrich Pfeffer
Publication date
01-08-2010
Publisher
Springer Netherlands
Published in
Clinical & Experimental Metastasis / Issue 6/2010
Print ISSN: 0262-0898
Electronic ISSN: 1573-7276
DOI
https://doi.org/10.1007/s10585-010-9312-5

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