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Published in: Clinical & Experimental Metastasis 8/2007

01-11-2007 | Research Paper

Soluble cadherins as cancer biomarkers

Authors: Olivier De Wever, Lara Derycke, An Hendrix, Gert De Meerleer, François Godeau, Herman Depypere, Marc Bracke

Published in: Clinical & Experimental Metastasis | Issue 8/2007

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Abstract

Molecular activities, regulating a balanced tissue organisation, are frequently disturbed during cancer progression. These include protein ectodomain shedding, a post-translational process that substantially changes the functional properties of the substrate protein. In comparison with normal epithelia, cancer cells almost invariably show diminished cadherin-mediated intercellular adhesion. This review will address cadherin ectodomain shedding and its functional consequence in normal physiology and in the tumor environment. Soluble cadherin fragments may retain specific biological activities during cancer cell invasion, angiogenesis and perineural invasion. When diffusion barriers disappear, soluble cadherins are detected in sera from cancer patients. Soluble N-(neural) cadherin may represent a novel diagnosis/prognostic biomarker showing a correlation with PSA in sera of prostate cancer patients. Furthermore, therapeutic monitoring in pancreas adenomacarcinoma revealed a correlation between circulating soluble N-cadherin and CA 19-9. A better understanding of cadherin regulation in cancer progression will likely increase our awareness of the importance of the combinatorial signals that regulate tissue integrity and eventually result in the identification of new therapeutics targeting cadherins.
Literature
2.
go back to reference Van Aken E, De Wever O, Correia da Rocha AS, Mareel M (2001) Defective E-cadherin/catenin complexes in human cancer. Virchows Arch 439:725–751PubMed Van Aken E, De Wever O, Correia da Rocha AS, Mareel M (2001) Defective E-cadherin/catenin complexes in human cancer. Virchows Arch 439:725–751PubMed
3.
4.
go back to reference Blobel CP (2005) ADAMs: key components in EGFR signalling and development. Nat Rev Mol Cell Biol 6:32–43PubMedCrossRef Blobel CP (2005) ADAMs: key components in EGFR signalling and development. Nat Rev Mol Cell Biol 6:32–43PubMedCrossRef
5.
go back to reference Seals DF, Courtneidge SA (2003) The ADAMs family of metalloproteases: multidomain proteins with multiple functions. Genes Dev 17:7–30PubMedCrossRef Seals DF, Courtneidge SA (2003) The ADAMs family of metalloproteases: multidomain proteins with multiple functions. Genes Dev 17:7–30PubMedCrossRef
6.
go back to reference Levi E, Fridman R, Miao H-Q et al (1996) Matrix metalloproteinase 2 releases active soluble ectodomain of fibroblast growth factor receptor 1. Proc Natl Acad Sci USA 93:7069–7074PubMedCrossRef Levi E, Fridman R, Miao H-Q et al (1996) Matrix metalloproteinase 2 releases active soluble ectodomain of fibroblast growth factor receptor 1. Proc Natl Acad Sci USA 93:7069–7074PubMedCrossRef
7.
go back to reference Vecchi M, Rudolph-Owen LA, Brown CL et al (1998) Tyrosine phosphorylation and proteolysis. Pervanadate-induced, metalloprotease-dependent cleavage of the ErbB-4 receptor and amphiregulin. J Biol Chem 273:20589–20595PubMedCrossRef Vecchi M, Rudolph-Owen LA, Brown CL et al (1998) Tyrosine phosphorylation and proteolysis. Pervanadate-induced, metalloprotease-dependent cleavage of the ErbB-4 receptor and amphiregulin. J Biol Chem 273:20589–20595PubMedCrossRef
8.
go back to reference Codony-Servat J, Albanell J, Lopez-Talavera JC et al (1999) Cleavage of the HER2 ectodomain is a pervanadate-activable process that is inhibited by the tissue inhibitor of metalloproteases-1 in breast cancer cells. Cancer Res 59:1196–1201PubMed Codony-Servat J, Albanell J, Lopez-Talavera JC et al (1999) Cleavage of the HER2 ectodomain is a pervanadate-activable process that is inhibited by the tissue inhibitor of metalloproteases-1 in breast cancer cells. Cancer Res 59:1196–1201PubMed
9.
go back to reference Nath D, Williamson NJ, Jarvis R, Murphy G (2001) Shedding of c-Met is regulated by crosstalk between a G-protein coupled receptor and the EGF receptor and is mediated by a TIMP-3 sensitive metalloproteinase. J Cell Sci 114:1213–1220PubMed Nath D, Williamson NJ, Jarvis R, Murphy G (2001) Shedding of c-Met is regulated by crosstalk between a G-protein coupled receptor and the EGF receptor and is mediated by a TIMP-3 sensitive metalloproteinase. J Cell Sci 114:1213–1220PubMed
10.
go back to reference Cavallaro U et al (2004) N-cadherin as an invasion promoter: a novel target for antitumor therapy? Curr Opin Investig Drugs 5:1274–1278PubMed Cavallaro U et al (2004) N-cadherin as an invasion promoter: a novel target for antitumor therapy? Curr Opin Investig Drugs 5:1274–1278PubMed
11.
go back to reference Noë V, Fingleton B, Jacobs K et al (2001) Release of an invasion promotor E-cadherin fragment by matrilysin and stromelysin-1. J Cell Sci 114:111–118PubMed Noë V, Fingleton B, Jacobs K et al (2001) Release of an invasion promotor E-cadherin fragment by matrilysin and stromelysin-1. J Cell Sci 114:111–118PubMed
12.
go back to reference Damsky CH, Richa J, Solter D et al (1983) Identification and purification of a cell surface glycoprotein mediating intercellular adhesion in embryonic and adult tissue. Cell 34:455–466PubMedCrossRef Damsky CH, Richa J, Solter D et al (1983) Identification and purification of a cell surface glycoprotein mediating intercellular adhesion in embryonic and adult tissue. Cell 34:455–466PubMedCrossRef
13.
go back to reference Wheelock MJ, Buck CA, Bechtol KB, Damsky CH (1987) Soluble 80-kd fragment of cell-CAM 120/80 disrupts cell-cell adhesion. J Cell Biochem 34:187–202PubMedCrossRef Wheelock MJ, Buck CA, Bechtol KB, Damsky CH (1987) Soluble 80-kd fragment of cell-CAM 120/80 disrupts cell-cell adhesion. J Cell Biochem 34:187–202PubMedCrossRef
14.
go back to reference Symowicz J, Adley BP, Gleason KJ et al (2007) Engagement of collagen-binding integrins promotes matrix metalloproteinase-9-dependent E-cadherin ectodomain shedding in ovarian carcinoma cells. Cancer Res 67:2030–2039PubMedCrossRef Symowicz J, Adley BP, Gleason KJ et al (2007) Engagement of collagen-binding integrins promotes matrix metalloproteinase-9-dependent E-cadherin ectodomain shedding in ovarian carcinoma cells. Cancer Res 67:2030–2039PubMedCrossRef
15.
go back to reference Davies G, Jiang WG, Mason MD (2001) Matrilysin mediates extracellular cleavage of E-cadherin from prostate cancer cells: a key mechanism in hepatocyte growth factor/scatter factor-induced cell-cell dissociation and in vitro invasion. Clin Cancer Res 7:3289–3297PubMed Davies G, Jiang WG, Mason MD (2001) Matrilysin mediates extracellular cleavage of E-cadherin from prostate cancer cells: a key mechanism in hepatocyte growth factor/scatter factor-induced cell-cell dissociation and in vitro invasion. Clin Cancer Res 7:3289–3297PubMed
16.
go back to reference Ryniers F, Stove C, Goethals M et al (2002) Plasmin produces an E-cadherin fragment that stimulates cancer cell invasion. Biol Chem 383:159–165PubMedCrossRef Ryniers F, Stove C, Goethals M et al (2002) Plasmin produces an E-cadherin fragment that stimulates cancer cell invasion. Biol Chem 383:159–165PubMedCrossRef
17.
go back to reference Hayashido Y, Hamana T, Yoshioka Y et al (2005) Plasminogen activator/plasmin system suppresses cell-cell adhesion of oral squamous cell carcinoma cells via proteolysis of E-cadherin. Int J Oncol 27:693–698PubMed Hayashido Y, Hamana T, Yoshioka Y et al (2005) Plasminogen activator/plasmin system suppresses cell-cell adhesion of oral squamous cell carcinoma cells via proteolysis of E-cadherin. Int J Oncol 27:693–698PubMed
18.
go back to reference Johnson SK, Ramani VC, Hennings L, Haun RS (2007) Kallikrein 7 enhances pancreatic cancer cell invasion by shedding E-cadherin. Cancer 109:1811–1820PubMedCrossRef Johnson SK, Ramani VC, Hennings L, Haun RS (2007) Kallikrein 7 enhances pancreatic cancer cell invasion by shedding E-cadherin. Cancer 109:1811–1820PubMedCrossRef
19.
go back to reference Covington MD, Burghardt RC, Parrish AR et al (2006) Ischemia-induced cleavage of cadherins in NRK cells requires MT1-MMP (MMP-14). Am J Physiol Renal Physiol 290:F43–F51PubMedCrossRef Covington MD, Burghardt RC, Parrish AR et al (2006) Ischemia-induced cleavage of cadherins in NRK cells requires MT1-MMP (MMP-14). Am J Physiol Renal Physiol 290:F43–F51PubMedCrossRef
20.
go back to reference Maretzky T, Reiss K, Ludwig A et al (2005) ADAM10 mediates E-cadherin shedding and regulates epithelial cell-cell adhesion, migration, and β-catenin translocation. Proc Natl Acad Sci USA 102:9182–9187PubMedCrossRef Maretzky T, Reiss K, Ludwig A et al (2005) ADAM10 mediates E-cadherin shedding and regulates epithelial cell-cell adhesion, migration, and β-catenin translocation. Proc Natl Acad Sci USA 102:9182–9187PubMedCrossRef
21.
go back to reference Steinhusen U, Weiske J, Badock V et al (2001) Cleavage and shedding of E-cadherin after induction of apoptosis. J Biol Chem 276:4972–4980PubMedCrossRef Steinhusen U, Weiske J, Badock V et al (2001) Cleavage and shedding of E-cadherin after induction of apoptosis. J Biol Chem 276:4972–4980PubMedCrossRef
22.
go back to reference Rashid MG, Sanda MG, Vallorosi CJ et al (2001) Posttranslational truncation and inactivation of human E-cadherin distinguishes prostate cancer from matched normal prostate. Cancer Res 61:489–492PubMed Rashid MG, Sanda MG, Vallorosi CJ et al (2001) Posttranslational truncation and inactivation of human E-cadherin distinguishes prostate cancer from matched normal prostate. Cancer Res 61:489–492PubMed
23.
go back to reference Rios-Doria J, Day KC, Kuefer R et al (2003) The role of calpain in the proteolytic cleavage of E-cadherin in prostate and mammary epithelial cells. J Biol Chem 278:1372–1379PubMedCrossRef Rios-Doria J, Day KC, Kuefer R et al (2003) The role of calpain in the proteolytic cleavage of E-cadherin in prostate and mammary epithelial cells. J Biol Chem 278:1372–1379PubMedCrossRef
24.
go back to reference Reiss K, Maretzky T, Ludwig A et al (2005) ADAM10 cleavage of N-cadherin and regulation of cell-cell adhesion and β-catenin nuclear signalling. EMBO J 24:742–752PubMedCrossRef Reiss K, Maretzky T, Ludwig A et al (2005) ADAM10 cleavage of N-cadherin and regulation of cell-cell adhesion and β-catenin nuclear signalling. EMBO J 24:742–752PubMedCrossRef
25.
go back to reference Monea S, Jordan BA, Srivastava S et al (2006) Membrane localization of membrane type 5 matrix metalloproteinase by AMPA receptor binding protein and cleavage of cadherins. J Neurosci 26:2300–2312PubMedCrossRef Monea S, Jordan BA, Srivastava S et al (2006) Membrane localization of membrane type 5 matrix metalloproteinase by AMPA receptor binding protein and cleavage of cadherins. J Neurosci 26:2300–2312PubMedCrossRef
26.
go back to reference Uemura K, Kihara T, Kuzuya A et al (2006) Characterization of sequential N-cadherin cleavage by ADAM10 and PS1. Neurosci Lett 402:278–283PubMedCrossRef Uemura K, Kihara T, Kuzuya A et al (2006) Characterization of sequential N-cadherin cleavage by ADAM10 and PS1. Neurosci Lett 402:278–283PubMedCrossRef
27.
go back to reference Paradies NE, Grunwald GB (1993) Purification and characterization of NCAD90, a soluble endogenous form of N-cadherin, which is generated by proteolysis during retinal development and retains adhesive and neurite-promoting function. J Neurosci Res 36:33–45PubMedCrossRef Paradies NE, Grunwald GB (1993) Purification and characterization of NCAD90, a soluble endogenous form of N-cadherin, which is generated by proteolysis during retinal development and retains adhesive and neurite-promoting function. J Neurosci Res 36:33–45PubMedCrossRef
28.
go back to reference Marambaud P, Wen PH, Dutt A et al (2003) A CBP binding transcriptional repressor produced by the PS1/epsilon-cleavage of N-cadherin is inhibited by PS1 FAD mutations. Cell 114:635–645PubMedCrossRef Marambaud P, Wen PH, Dutt A et al (2003) A CBP binding transcriptional repressor produced by the PS1/epsilon-cleavage of N-cadherin is inhibited by PS1 FAD mutations. Cell 114:635–645PubMedCrossRef
29.
go back to reference Shoval I, Ludwig A, Kalcheim C (2007) Antagonistic roles of full-length N-cadherin and its soluble BMP cleavage product in neural crest delamination. Development 134:491–501PubMedCrossRef Shoval I, Ludwig A, Kalcheim C (2007) Antagonistic roles of full-length N-cadherin and its soluble BMP cleavage product in neural crest delamination. Development 134:491–501PubMedCrossRef
30.
go back to reference Tai C-Y, Mysore SP, Chiu C, Schuman EM (2007) Activity-regulated N-cadherin endocytosis. Neuron 54:771–785PubMedCrossRef Tai C-Y, Mysore SP, Chiu C, Schuman EM (2007) Activity-regulated N-cadherin endocytosis. Neuron 54:771–785PubMedCrossRef
31.
go back to reference Uemura K, Kuzuya A, Aoyagi N et al (2007) Amyloid β inhibits ectodomain shedding of N-cadherin via down-regulation of cell-surface NMDA receptor. Neuroscience 145:5–10PubMedCrossRef Uemura K, Kuzuya A, Aoyagi N et al (2007) Amyloid β inhibits ectodomain shedding of N-cadherin via down-regulation of cell-surface NMDA receptor. Neuroscience 145:5–10PubMedCrossRef
32.
go back to reference Noë V, Willems J, Vandekerckhove J et al (1999) Inhibition of adhesion and induction of epithelial cell invasion by HAV-containing E-cadherin-specific peptides. J Cell Sci 112:127–135PubMed Noë V, Willems J, Vandekerckhove J et al (1999) Inhibition of adhesion and induction of epithelial cell invasion by HAV-containing E-cadherin-specific peptides. J Cell Sci 112:127–135PubMed
33.
go back to reference Nawrocki-Raby B, Gilles C, Polette M et al (2003) Upregulation of MMPs by soluble E-cadherin in human lung tumor cells. Int J Cancer 105:790–795PubMedCrossRef Nawrocki-Raby B, Gilles C, Polette M et al (2003) Upregulation of MMPs by soluble E-cadherin in human lung tumor cells. Int J Cancer 105:790–795PubMedCrossRef
34.
go back to reference Lee KH, Choi EY, Hyun MS et al (2007) Association of extracellular cleavage of E-cadherin mediated by MMP-7 with HGF-induced in vitro invasion in human stomach cancer cells. Eur Surg Res 39:208–215PubMedCrossRef Lee KH, Choi EY, Hyun MS et al (2007) Association of extracellular cleavage of E-cadherin mediated by MMP-7 with HGF-induced in vitro invasion in human stomach cancer cells. Eur Surg Res 39:208–215PubMedCrossRef
35.
go back to reference Derycke L, Morbidelli L, Ziche M et al (2006) Soluble N-cadherin fragment promotes angiogenesis. Clin Exp Metastasis 23:187–201PubMedCrossRef Derycke L, Morbidelli L, Ziche M et al (2006) Soluble N-cadherin fragment promotes angiogenesis. Clin Exp Metastasis 23:187–201PubMedCrossRef
36.
go back to reference De Wever O, Westbroek W, Verloes A et al (2004) Critical role of N-cadherin in myofibroblast invasion and migration in vitro stimulated by colon-cancer-cell-derived TGF-β or wounding. J Cell Sci 117:4691–4703PubMedCrossRef De Wever O, Westbroek W, Verloes A et al (2004) Critical role of N-cadherin in myofibroblast invasion and migration in vitro stimulated by colon-cancer-cell-derived TGF-β or wounding. J Cell Sci 117:4691–4703PubMedCrossRef
37.
go back to reference Utton MA, Eickholt B, Howell FV et al (2001) Soluble N-cadherin stimulates fibroblast growth factor receptor dependent neurite outgrowth and N-cadherin and the fibroblast growth factor receptor co-cluster in cells. J Neurochem 76:1421–1430PubMedCrossRef Utton MA, Eickholt B, Howell FV et al (2001) Soluble N-cadherin stimulates fibroblast growth factor receptor dependent neurite outgrowth and N-cadherin and the fibroblast growth factor receptor co-cluster in cells. J Neurochem 76:1421–1430PubMedCrossRef
38.
go back to reference Cifuentes-Diaz C, Nicolet M, Goudou D et al (1994) N-cadherin expression in developing, adult and denervated chicken neuromuscular system: accumulations at both the neuromuscular junction and the node of Ranvier. Development 120:1–11PubMed Cifuentes-Diaz C, Nicolet M, Goudou D et al (1994) N-cadherin expression in developing, adult and denervated chicken neuromuscular system: accumulations at both the neuromuscular junction and the node of Ranvier. Development 120:1–11PubMed
39.
go back to reference Whittard JD, Craig SE, Mould AP et al (2002) E-cadherin is a ligand for integrin α2ß1. Matrix Biol 21:525–532PubMedCrossRef Whittard JD, Craig SE, Mould AP et al (2002) E-cadherin is a ligand for integrin α2ß1. Matrix Biol 21:525–532PubMedCrossRef
40.
go back to reference De Wever O, Mareel M (2006) Pro-invasive molecular cross-signaling between cancer cells and myofibroblasts. In: Chaponnier C, Desmoulière A, Gabbiani G (eds) Tissue Repair, Contraction and the Myofibroblast, Chapt. 8. Eurekah.com and Springer Science+Business Media, pp 74–87 De Wever O, Mareel M (2006) Pro-invasive molecular cross-signaling between cancer cells and myofibroblasts. In: Chaponnier C, Desmoulière A, Gabbiani G (eds) Tissue Repair, Contraction and the Myofibroblast, Chapt. 8. Eurekah.com and Springer Science+Business Media, pp 74–87
41.
go back to reference De Wever O, Nguyen Q-D, Van Hoorde L et al (2004) Tenascin-C and SF/HGF produced by myofibroblasts in vitro provide convergent pro-invasive signals to human colon cancer cells through RhoA and Rac. FASEB J 18:1016–1018PubMed De Wever O, Nguyen Q-D, Van Hoorde L et al (2004) Tenascin-C and SF/HGF produced by myofibroblasts in vitro provide convergent pro-invasive signals to human colon cancer cells through RhoA and Rac. FASEB J 18:1016–1018PubMed
42.
go back to reference Egeblad M, Werb Z (2002) New functions for the matrix metalloproteinases in cancer progression. Nat Rev Cancer 2:161–174PubMedCrossRef Egeblad M, Werb Z (2002) New functions for the matrix metalloproteinases in cancer progression. Nat Rev Cancer 2:161–174PubMedCrossRef
43.
44.
go back to reference Poulsom R, Pignatelli M, Stetler-Stevenson WG et al (1992) Stromal expression of 72 kDa type IV collagenase (MMP-2) and TIMP-2 mRNAs in colorectal neoplasia. Am J Pathol 141:389–396PubMed Poulsom R, Pignatelli M, Stetler-Stevenson WG et al (1992) Stromal expression of 72 kDa type IV collagenase (MMP-2) and TIMP-2 mRNAs in colorectal neoplasia. Am J Pathol 141:389–396PubMed
45.
go back to reference Pyke C, Ralfkiaer E, Tryggvason K, Danø K (1993) Messenger RNA for two type IV collagenases is located in stromal cells in human colon cancer. Am J Pathol 142:359–365PubMed Pyke C, Ralfkiaer E, Tryggvason K, Danø K (1993) Messenger RNA for two type IV collagenases is located in stromal cells in human colon cancer. Am J Pathol 142:359–365PubMed
46.
go back to reference Shintani Y, Wheelock MJ, Johnson KR (2006) Phosphoinositide-3 kinase-Rac1-c-Jun NH2-terminal kinase signaling mediates collagen I-induced cell scattering and up-regulation of N-cadherin expression in mouse mammary epithelial cells. Mol Biol Cell 17:2963–2975PubMedCrossRef Shintani Y, Wheelock MJ, Johnson KR (2006) Phosphoinositide-3 kinase-Rac1-c-Jun NH2-terminal kinase signaling mediates collagen I-induced cell scattering and up-regulation of N-cadherin expression in mouse mammary epithelial cells. Mol Biol Cell 17:2963–2975PubMedCrossRef
47.
go back to reference Shintani Y, Hollingsworth MA, Wheelock MJ, Johnson KR (2006) Collagen I promotes metastasis in pancreatic cancer by activating c-Jun NH2-terminal kinase 1 and up-regulating N-cadherin expression. Cancer Res 66:11745–11753PubMedCrossRef Shintani Y, Hollingsworth MA, Wheelock MJ, Johnson KR (2006) Collagen I promotes metastasis in pancreatic cancer by activating c-Jun NH2-terminal kinase 1 and up-regulating N-cadherin expression. Cancer Res 66:11745–11753PubMedCrossRef
48.
go back to reference Koenig A, Mueller C, Hasel C et al (2006) Collagen type I induces disruption of E-cadherin-mediated cell-cell contacts and promotes proliferation of pancreatic carcinoma cells. Cancer Res 66:4662–4671PubMedCrossRef Koenig A, Mueller C, Hasel C et al (2006) Collagen type I induces disruption of E-cadherin-mediated cell-cell contacts and promotes proliferation of pancreatic carcinoma cells. Cancer Res 66:4662–4671PubMedCrossRef
49.
go back to reference Navarro P, Ruco L, Dejana E (1998) Differential localization of VE- and N-cadherins in human endothelial cells: VE-cadherin competes with N-cadherin for junctional localization. J Cell Biol 140:1475–1484PubMedCrossRef Navarro P, Ruco L, Dejana E (1998) Differential localization of VE- and N-cadherins in human endothelial cells: VE-cadherin competes with N-cadherin for junctional localization. J Cell Biol 140:1475–1484PubMedCrossRef
50.
go back to reference Gerhardt H, Wolburg H, Redies C (2000) N-cadherin mediates pericytic-endothelial interaction during brain angiogenesis in the chicken. Dev Dyn 218:472–479PubMedCrossRef Gerhardt H, Wolburg H, Redies C (2000) N-cadherin mediates pericytic-endothelial interaction during brain angiogenesis in the chicken. Dev Dyn 218:472–479PubMedCrossRef
51.
go back to reference Luo Y, Radice GL (2005) N-cadherin acts upstream of VE-cadherin in controlling vascular morphogenesis. J Cell Biol 169:29–34PubMedCrossRef Luo Y, Radice GL (2005) N-cadherin acts upstream of VE-cadherin in controlling vascular morphogenesis. J Cell Biol 169:29–34PubMedCrossRef
52.
go back to reference Carmeliet P, Lampugnani M-G, Moons L et al (1999) Targeted deficiency or cytosolic truncation of the VE-cadherin gene in mice impairs VEGF-mediated endothelial survival and angiogenesis. Cell 98:147–157PubMedCrossRef Carmeliet P, Lampugnani M-G, Moons L et al (1999) Targeted deficiency or cytosolic truncation of the VE-cadherin gene in mice impairs VEGF-mediated endothelial survival and angiogenesis. Cell 98:147–157PubMedCrossRef
53.
go back to reference Paik J-H, Skoura A, Chae S-S et al (2004) Sphingosine 1-phosphate receptor regulation of N-cadherin mediates vascular stabilization. Genes Dev 18:2392–2403PubMedCrossRef Paik J-H, Skoura A, Chae S-S et al (2004) Sphingosine 1-phosphate receptor regulation of N-cadherin mediates vascular stabilization. Genes Dev 18:2392–2403PubMedCrossRef
54.
go back to reference Harnden P, Shelley MD, Clements H et al (2007) The prognostic significance of perineural invasion in prostatic cancer biopsies. A systematic review. Cancer 109:13–24PubMedCrossRef Harnden P, Shelley MD, Clements H et al (2007) The prognostic significance of perineural invasion in prostatic cancer biopsies. A systematic review. Cancer 109:13–24PubMedCrossRef
55.
go back to reference Ayala GE, Wheeler TM, Shine HD et al (2001) In vitro dorsal root ganglia and human prostate cell line interaction: redefining perineural invasion in prostate cancer. Prostate 49:213–223PubMedCrossRef Ayala GE, Wheeler TM, Shine HD et al (2001) In vitro dorsal root ganglia and human prostate cell line interaction: redefining perineural invasion in prostate cancer. Prostate 49:213–223PubMedCrossRef
56.
go back to reference Ayala GE, Dai H, Ittmann M et al (2004) Growth and survival mechanisms associated with perineural invasion in prostate cancer. Cancer Res 64:6082–6090PubMedCrossRef Ayala GE, Dai H, Ittmann M et al (2004) Growth and survival mechanisms associated with perineural invasion in prostate cancer. Cancer Res 64:6082–6090PubMedCrossRef
57.
go back to reference Takeichi M (1991) Cadherin cell adhesion receptors as a morphogenetic regulator. Science 251:1451–1455PubMedCrossRef Takeichi M (1991) Cadherin cell adhesion receptors as a morphogenetic regulator. Science 251:1451–1455PubMedCrossRef
58.
go back to reference Tran NL, Adams DG, Vaillancourt RR, Heimark RL (2002) Signal Transduction from N-cadherin Increases Bcl-2. Regulation of the phosphatidylinositol 3-kinase/Akt pathway by homophilic adhesion and actin cytoskeletal organization. J Biol Chem 277:32905–32914PubMedCrossRef Tran NL, Adams DG, Vaillancourt RR, Heimark RL (2002) Signal Transduction from N-cadherin Increases Bcl-2. Regulation of the phosphatidylinositol 3-kinase/Akt pathway by homophilic adhesion and actin cytoskeletal organization. J Biol Chem 277:32905–32914PubMedCrossRef
59.
go back to reference Ayala GE, Dai H, Tahir SA et al (2006) Stromal antiapoptotic paracrine loop in perineural invasion of prostatic carcinoma. Cancer Res 66:5159–5164PubMedCrossRef Ayala GE, Dai H, Tahir SA et al (2006) Stromal antiapoptotic paracrine loop in perineural invasion of prostatic carcinoma. Cancer Res 66:5159–5164PubMedCrossRef
60.
go back to reference Suyama K, Shapiro I, Guttman M, Hazan RB (2002) A signaling pathway leading to metastasis is controlled by N-cadherin and the FGF receptor. Cancer Cell 2:301–314PubMedCrossRef Suyama K, Shapiro I, Guttman M, Hazan RB (2002) A signaling pathway leading to metastasis is controlled by N-cadherin and the FGF receptor. Cancer Cell 2:301–314PubMedCrossRef
61.
go back to reference Weeraratna AT, Jiang Y, Hostetter G et al (2002) Wnt5a signaling directly affects cell motility and invasion of metastatic melanoma. Cancer Cell 1:279–288PubMedCrossRef Weeraratna AT, Jiang Y, Hostetter G et al (2002) Wnt5a signaling directly affects cell motility and invasion of metastatic melanoma. Cancer Cell 1:279–288PubMedCrossRef
62.
go back to reference Rodrigues S, De Wever O, Bruyneel E et al (2007) Opposing roles of netrin-1 and the dependence receptor DCC in cancer cell invasion, tumor growth and metastasis. Oncogene 26:5615–5625PubMedCrossRef Rodrigues S, De Wever O, Bruyneel E et al (2007) Opposing roles of netrin-1 and the dependence receptor DCC in cancer cell invasion, tumor growth and metastasis. Oncogene 26:5615–5625PubMedCrossRef
63.
go back to reference Giordano S, Corso S, Conrotto P et al (2002) The Semaphorin 4D receptor controls invasive growth by coupling with Met. Nat Cell Biol 4:720–724PubMedCrossRef Giordano S, Corso S, Conrotto P et al (2002) The Semaphorin 4D receptor controls invasive growth by coupling with Met. Nat Cell Biol 4:720–724PubMedCrossRef
64.
go back to reference Cornell RJ, Rowley D, Wheeler T et al (2003) Neuroepithelial interactions in prostate cancer are enhanced in the presence ofprostatic stroma. Urology 61:870–875PubMedCrossRef Cornell RJ, Rowley D, Wheeler T et al (2003) Neuroepithelial interactions in prostate cancer are enhanced in the presence ofprostatic stroma. Urology 61:870–875PubMedCrossRef
65.
go back to reference Dalton WS, Friend SH (2006) Cancer biomarkers - an invitation to the table. Science 312:1165–1168PubMedCrossRef Dalton WS, Friend SH (2006) Cancer biomarkers - an invitation to the table. Science 312:1165–1168PubMedCrossRef
66.
go back to reference Joensuu H, Anttonen A, Eriksson M et al (2002) Soluble syndecan-1 and serum basic fibroblast growth factor are new prognostic factors in lung cancer. Cancer Res 62:5210–5217PubMed Joensuu H, Anttonen A, Eriksson M et al (2002) Soluble syndecan-1 and serum basic fibroblast growth factor are new prognostic factors in lung cancer. Cancer Res 62:5210–5217PubMed
67.
go back to reference Seidel C, Sundan A, Hjorth M et al (2000) Serum syndecan-1: a new independent prognostic marker in multiple myeloma. Blood 95:388–392PubMed Seidel C, Sundan A, Hjorth M et al (2000) Serum syndecan-1: a new independent prognostic marker in multiple myeloma. Blood 95:388–392PubMed
68.
go back to reference Tartour E, Mosseri V, Jouffroy T et al (2001) Serum soluble interleukin-2 receptor concentrations as an independent prognostic marker in head and neck cancer. Lancet 357:1263–1264PubMedCrossRef Tartour E, Mosseri V, Jouffroy T et al (2001) Serum soluble interleukin-2 receptor concentrations as an independent prognostic marker in head and neck cancer. Lancet 357:1263–1264PubMedCrossRef
69.
go back to reference Witkowska AM (2005) On the role of sIL-2R measurements in rheumatoid arthritis and cancers. Mediators Inflamm 2005:121–130PubMedCrossRef Witkowska AM (2005) On the role of sIL-2R measurements in rheumatoid arthritis and cancers. Mediators Inflamm 2005:121–130PubMedCrossRef
70.
go back to reference Chan AOO, Lam SK, Chu KM et al (2001) Soluble E-cadherin is a valid prognostic marker in gastric carcinoma. Gut 48:808–811PubMedCrossRef Chan AOO, Lam SK, Chu KM et al (2001) Soluble E-cadherin is a valid prognostic marker in gastric carcinoma. Gut 48:808–811PubMedCrossRef
71.
go back to reference Velikova G, Banks RE, Gearing A et al (1997) Circulating soluble adhesion molecules E-cadherin, E-selectin, intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) in patients with gastric cancer. Br J Cancer 76:1398–1404PubMed Velikova G, Banks RE, Gearing A et al (1997) Circulating soluble adhesion molecules E-cadherin, E-selectin, intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) in patients with gastric cancer. Br J Cancer 76:1398–1404PubMed
72.
go back to reference Gofuku J, Shiozaki H, Doki Y et al (1998) Characterization of soluble E-cadherin as a disease marker in gastric cancer patients. Br J Cancer 78:1095–1101PubMed Gofuku J, Shiozaki H, Doki Y et al (1998) Characterization of soluble E-cadherin as a disease marker in gastric cancer patients. Br J Cancer 78:1095–1101PubMed
73.
go back to reference Chan AO-O, Chu K-M, Lam S-K et al (2003) Soluble E-cadherin is an independent pretherapeutic factor for long-term survival in gastric cancer. J Clin Oncol 21:2288–2293PubMedCrossRef Chan AO-O, Chu K-M, Lam S-K et al (2003) Soluble E-cadherin is an independent pretherapeutic factor for long-term survival in gastric cancer. J Clin Oncol 21:2288–2293PubMedCrossRef
74.
go back to reference Juhasz M, Ebert MPA, Schulz HU et al (2003) Dual role of serum soluble E-cadherin as a biological marker of metastatic development in gastric cancer. Scand J Gastroenterol 38:850–855PubMedCrossRef Juhasz M, Ebert MPA, Schulz HU et al (2003) Dual role of serum soluble E-cadherin as a biological marker of metastatic development in gastric cancer. Scand J Gastroenterol 38:850–855PubMedCrossRef
75.
go back to reference Chan AOO, Chu K-M, Lam SK et al (2005) Early prediction of tumor recurrence after curative resection of gastric carcinoma by measuring soluble E-cadherin. Cancer 104:740–746PubMedCrossRef Chan AOO, Chu K-M, Lam SK et al (2005) Early prediction of tumor recurrence after curative resection of gastric carcinoma by measuring soluble E-cadherin. Cancer 104:740–746PubMedCrossRef
76.
go back to reference Griffiths TRL, Brotherick I, Bishop RI et al (1996) Cell adhesion molecules in bladder cancer: soluble serum E-cadherin correlates with predictors of recurrence. Br J Cancer 74:579–584PubMed Griffiths TRL, Brotherick I, Bishop RI et al (1996) Cell adhesion molecules in bladder cancer: soluble serum E-cadherin correlates with predictors of recurrence. Br J Cancer 74:579–584PubMed
77.
go back to reference Durkan GC, Brotherick I, Mellon JK (1999) The impact of transurethral resection of bladder tumour on serum levels of soluble E-cadherin. BJU Int 83:424–428PubMedCrossRef Durkan GC, Brotherick I, Mellon JK (1999) The impact of transurethral resection of bladder tumour on serum levels of soluble E-cadherin. BJU Int 83:424–428PubMedCrossRef
78.
go back to reference Matsumoto K, Shariat SF, Casella R et al (2003) Preoperative plasma soluble E-cadherin predicts metastases to lymph nodes and prognosis in patients undergoing radical cystectomy. J Urol 170:2248–2252PubMedCrossRef Matsumoto K, Shariat SF, Casella R et al (2003) Preoperative plasma soluble E-cadherin predicts metastases to lymph nodes and prognosis in patients undergoing radical cystectomy. J Urol 170:2248–2252PubMedCrossRef
79.
go back to reference Kuefer R, Hofer MD, Gschwend JE et al (2003) The role of an 80 kDa fragment of E-cadherin in the metastatic progression of prostate cancer. Clin Cancer Res 9:6447–6452PubMed Kuefer R, Hofer MD, Gschwend JE et al (2003) The role of an 80 kDa fragment of E-cadherin in the metastatic progression of prostate cancer. Clin Cancer Res 9:6447–6452PubMed
80.
go back to reference Kuefer R, Hofer MD, Zorn CSM et al (2005) Assessment of a fragment of e-cadherin as a serum biomarker with predictive value for prostate cancer. Br J Cancer 92:2018–2023PubMedCrossRef Kuefer R, Hofer MD, Zorn CSM et al (2005) Assessment of a fragment of e-cadherin as a serum biomarker with predictive value for prostate cancer. Br J Cancer 92:2018–2023PubMedCrossRef
81.
go back to reference Gadducci A, Ferdeghini M, Cosio S et al (1999) Preoperative serum E-cadherin assay in patients with ovarian carcinoma. Anticancer Res 19:769–772PubMed Gadducci A, Ferdeghini M, Cosio S et al (1999) Preoperative serum E-cadherin assay in patients with ovarian carcinoma. Anticancer Res 19:769–772PubMed
82.
go back to reference Velikova G, Banks RE, Gearing A et al (1998) Serum concentrations of soluble adhesion molecules in patients with colorectal cancer. Br J Cancer 77:1857–1863PubMed Velikova G, Banks RE, Gearing A et al (1998) Serum concentrations of soluble adhesion molecules in patients with colorectal cancer. Br J Cancer 77:1857–1863PubMed
83.
go back to reference Wilmanns C, Grossmann J, Steinhauer S et al (2004) Soluble serum E-cadherin as a marker of tumour progression in colorectal cancer patients. Clin Exp Metastasis 21:75–78PubMedCrossRef Wilmanns C, Grossmann J, Steinhauer S et al (2004) Soluble serum E-cadherin as a marker of tumour progression in colorectal cancer patients. Clin Exp Metastasis 21:75–78PubMedCrossRef
84.
go back to reference Shirahama S, Furukawa F, Wakita H, Takigawa M (1996) E- and P-cadherin expression in tumor tissues and soluble E-cadherin levels in sera of patients with skin cancer. J Dermatol Sci 13:30–36PubMedCrossRef Shirahama S, Furukawa F, Wakita H, Takigawa M (1996) E- and P-cadherin expression in tumor tissues and soluble E-cadherin levels in sera of patients with skin cancer. J Dermatol Sci 13:30–36PubMedCrossRef
85.
go back to reference Billion K, Ibrahim H, Mauch C, Niessen CM (2006) Increased soluble E-cadherin in melanoma patients. Skin Pharmacol Physiol 19:65–70PubMedCrossRef Billion K, Ibrahim H, Mauch C, Niessen CM (2006) Increased soluble E-cadherin in melanoma patients. Skin Pharmacol Physiol 19:65–70PubMedCrossRef
86.
go back to reference Charalabopoulos K, Gogali A, Dalavaga Y et al (2006) The clinical significance of soluble E-cadherin in nonsmall cell lung cancer. Exp Oncol 28:83–85PubMed Charalabopoulos K, Gogali A, Dalavaga Y et al (2006) The clinical significance of soluble E-cadherin in nonsmall cell lung cancer. Exp Oncol 28:83–85PubMed
87.
go back to reference Banks RE, Porter WH, Whelan P et al (1995) Soluble forms of the adhesion molecule E-cadherin in urine. J Clin Pathol 48:179–180PubMedCrossRef Banks RE, Porter WH, Whelan P et al (1995) Soluble forms of the adhesion molecule E-cadherin in urine. J Clin Pathol 48:179–180PubMedCrossRef
88.
go back to reference Protheroe AS, Banks RE, Mzimba M et al (1999) Urinary concentrations of the soluble adhesion molecule E-cadherin and total protein in patients with bladder cancer. Br J Cancer 80:273–278PubMedCrossRef Protheroe AS, Banks RE, Mzimba M et al (1999) Urinary concentrations of the soluble adhesion molecule E-cadherin and total protein in patients with bladder cancer. Br J Cancer 80:273–278PubMedCrossRef
89.
go back to reference Daraï E, Bringuier A-F, Walker-Combrouze F et al (1998) Soluble adhesion molecules in serum and cyst fluid from patients with cystic tumours of the ovary. Hum Reprod 13:2831–2835PubMedCrossRef Daraï E, Bringuier A-F, Walker-Combrouze F et al (1998) Soluble adhesion molecules in serum and cyst fluid from patients with cystic tumours of the ovary. Hum Reprod 13:2831–2835PubMedCrossRef
90.
go back to reference Sundfeldt K, Ivarsson K, Rask K et al (2001) Higher levels of soluble E-cadherin in cyst fluid from malignant ovarian tumours than in benign cysts. Anticancer Res 21:65–70PubMed Sundfeldt K, Ivarsson K, Rask K et al (2001) Higher levels of soluble E-cadherin in cyst fluid from malignant ovarian tumours than in benign cysts. Anticancer Res 21:65–70PubMed
91.
go back to reference Knudsen KA, Lin CY, Johnson KR et al (2000) Lack of correlation between serum levels of E- and P-cadherin fragments and the presence of breast cancer. Hum Pathol 31:961–965PubMedCrossRef Knudsen KA, Lin CY, Johnson KR et al (2000) Lack of correlation between serum levels of E- and P-cadherin fragments and the presence of breast cancer. Hum Pathol 31:961–965PubMedCrossRef
92.
go back to reference Sulkowska M, Famulski W, Wincewicz A et al (2006) Levels of VE-cadherin increase independently of VEGF in preoperative sera of patients with colorectal cancer. Tumori 92:67–71PubMed Sulkowska M, Famulski W, Wincewicz A et al (2006) Levels of VE-cadherin increase independently of VEGF in preoperative sera of patients with colorectal cancer. Tumori 92:67–71PubMed
93.
go back to reference Derycke L, De Wever O, Stove V et al (2006) Soluble N-cadherin in human biological fluids. Int J Cancer 119:2895–2900PubMedCrossRef Derycke L, De Wever O, Stove V et al (2006) Soluble N-cadherin in human biological fluids. Int J Cancer 119:2895–2900PubMedCrossRef
94.
go back to reference Pittard AJ, Banks RE, Galley HF, Webster NR (1996) Soluble E-cadherin concentrations in patients with systemic inflammatory response syndrome and multiorgan dysfunction syndrome. Br J Anaesth 76:629–631PubMed Pittard AJ, Banks RE, Galley HF, Webster NR (1996) Soluble E-cadherin concentrations in patients with systemic inflammatory response syndrome and multiorgan dysfunction syndrome. Br J Anaesth 76:629–631PubMed
95.
go back to reference Soler AP, Russo J, Russo IH, Knudsen KA (2002) Soluble fragment of P-cadherin adhesion protein found in human milk. J Cell Biochem 85:180–184PubMedCrossRef Soler AP, Russo J, Russo IH, Knudsen KA (2002) Soluble fragment of P-cadherin adhesion protein found in human milk. J Cell Biochem 85:180–184PubMedCrossRef
96.
go back to reference De Paul AL, Bonaterra M, Soler AP et al (2005) Soluble P-cadherin found in human semen. J Androl 26:44–47PubMed De Paul AL, Bonaterra M, Soler AP et al (2005) Soluble P-cadherin found in human semen. J Androl 26:44–47PubMed
97.
go back to reference Soeki T, Tamura Y, Shinohara H et al (2004) Elevated concentration of soluble vascular endothelial cadherin is associated with coronary atherosclerosis. Circ J 68:1–5PubMedCrossRef Soeki T, Tamura Y, Shinohara H et al (2004) Elevated concentration of soluble vascular endothelial cadherin is associated with coronary atherosclerosis. Circ J 68:1–5PubMedCrossRef
98.
go back to reference Lafky JM, Baron AT, Cora EM et al (2005) Serum soluble epidermal growth factor receptor concentrations decrease in postmenopausal metastatic breast cancer patients treated with letrozole. Cancer Res 65:3059–3062PubMed Lafky JM, Baron AT, Cora EM et al (2005) Serum soluble epidermal growth factor receptor concentrations decrease in postmenopausal metastatic breast cancer patients treated with letrozole. Cancer Res 65:3059–3062PubMed
99.
go back to reference Derycke LDM, Bracke ME (2004) N-cadherin in the spotlight of cell-cell adhesion, differentiation, embryogenesis, invasion and signalling. Int J Dev Biol 48:463–476PubMedCrossRef Derycke LDM, Bracke ME (2004) N-cadherin in the spotlight of cell-cell adhesion, differentiation, embryogenesis, invasion and signalling. Int J Dev Biol 48:463–476PubMedCrossRef
100.
go back to reference Zhang B, Groffen J, Heisterkamp N (2007) Increased resistance to a farnesyltransferase inhibitor by N-cadherin expression in Bcr/Abl-P190 lymphoblastic leukemia cells. Leukemia 21:1189–1197PubMedCrossRef Zhang B, Groffen J, Heisterkamp N (2007) Increased resistance to a farnesyltransferase inhibitor by N-cadherin expression in Bcr/Abl-P190 lymphoblastic leukemia cells. Leukemia 21:1189–1197PubMedCrossRef
101.
go back to reference Hulit J, Suyama K, Chung S et al (2007) N-cadherin signaling potentiates mammary tumor metastasis via enhanced extracellular signal-regulated kinase activation. Cancer Res 67:3106–3116PubMedCrossRef Hulit J, Suyama K, Chung S et al (2007) N-cadherin signaling potentiates mammary tumor metastasis via enhanced extracellular signal-regulated kinase activation. Cancer Res 67:3106–3116PubMedCrossRef
102.
go back to reference Williams E, Williams G, Gour BJ et al (2000) A novel family of cyclic peptide antagonists suggests that N-cadherin specificity is determined by amino acids that flank the HAV motif. J Biol Chem 275:4007–4012PubMedCrossRef Williams E, Williams G, Gour BJ et al (2000) A novel family of cyclic peptide antagonists suggests that N-cadherin specificity is determined by amino acids that flank the HAV motif. J Biol Chem 275:4007–4012PubMedCrossRef
103.
go back to reference Williams G, Williams E-J, Doherty P (2002) Dimeric versions of two short N-cadherin binding motifs (HAVDI and INPISG) function as N-cadherin agonists. J Biol Chem 277:4361–4367PubMedCrossRef Williams G, Williams E-J, Doherty P (2002) Dimeric versions of two short N-cadherin binding motifs (HAVDI and INPISG) function as N-cadherin agonists. J Biol Chem 277:4361–4367PubMedCrossRef
104.
go back to reference Mariotti A, Perotti A, Sessa C, Rüegg C (2007) N-cadherin as a therapeutic target in cancer. Expert Opin Investig Drugs 16:451–465PubMedCrossRef Mariotti A, Perotti A, Sessa C, Rüegg C (2007) N-cadherin as a therapeutic target in cancer. Expert Opin Investig Drugs 16:451–465PubMedCrossRef
105.
go back to reference Tomita K, van Bokhoven A, van Leenders GJLH et al (2000) Cadherin switching in human prostate cancer progression. Cancer Res 60:3650–3654PubMed Tomita K, van Bokhoven A, van Leenders GJLH et al (2000) Cadherin switching in human prostate cancer progression. Cancer Res 60:3650–3654PubMed
106.
go back to reference Lee DM, Kiener HP, Agarwal SK et al (2007) Cadherin-11 in synovial lining formation and pathology in arthritis. Science 315:1006–1010PubMedCrossRef Lee DM, Kiener HP, Agarwal SK et al (2007) Cadherin-11 in synovial lining formation and pathology in arthritis. Science 315:1006–1010PubMedCrossRef
107.
go back to reference Williams E-J, Williams G, Howell FV et al (2001) Identification of an N-cadherin motif that can interact with the fibroblast growth factor receptor and is required for axonal growth. J Biol Chem 276:43879–43886PubMedCrossRef Williams E-J, Williams G, Howell FV et al (2001) Identification of an N-cadherin motif that can interact with the fibroblast growth factor receptor and is required for axonal growth. J Biol Chem 276:43879–43886PubMedCrossRef
108.
go back to reference Kim J-B, Islam S, Kim YJ et al (2000) N-Cadherin extracellular repeat 4 mediates epithelial to mesenchymal transition and increased motility. J Cell Biol 151:1193–1206PubMedCrossRef Kim J-B, Islam S, Kim YJ et al (2000) N-Cadherin extracellular repeat 4 mediates epithelial to mesenchymal transition and increased motility. J Cell Biol 151:1193–1206PubMedCrossRef
109.
go back to reference D’Amato RJ, Loughnan MS, Flynn E, Folkman J (1994) Thalidomide is an inhibitor of angiogenesis. Proc Natl Acad Sci USA 91:4082–4085PubMedCrossRef D’Amato RJ, Loughnan MS, Flynn E, Folkman J (1994) Thalidomide is an inhibitor of angiogenesis. Proc Natl Acad Sci USA 91:4082–4085PubMedCrossRef
110.
go back to reference Thiele A, Thormann M, Hofmann H-J et al (2000) A possible role of N-cadherin in thalidomide teratogenicity. Life Sci 67:457–461PubMedCrossRef Thiele A, Thormann M, Hofmann H-J et al (2000) A possible role of N-cadherin in thalidomide teratogenicity. Life Sci 67:457–461PubMedCrossRef
111.
go back to reference Anderson KC (2007) Targeted therapy of multiple myeloma based upon tumor-microenvironmental interactions. Exp Hematol 35:155–162PubMedCrossRef Anderson KC (2007) Targeted therapy of multiple myeloma based upon tumor-microenvironmental interactions. Exp Hematol 35:155–162PubMedCrossRef
112.
go back to reference Gupta D, Treon SP, Shima Y et al (2001) Adherence of multiple myeloma cells to bone marrow stromal cells upregulates vascular endothelial growth factor secretion: therapeutic applications. Leukemia 15:1950–1961PubMed Gupta D, Treon SP, Shima Y et al (2001) Adherence of multiple myeloma cells to bone marrow stromal cells upregulates vascular endothelial growth factor secretion: therapeutic applications. Leukemia 15:1950–1961PubMed
113.
go back to reference Visentin B, Vekich JA, Sibbald BJ et al (2006) Validation of an anti-sphingosine-1-phosphate antibody as a potential therapeutic in reducing growth, invasion, and angiogenesis in multiple tumor lineages. Cancer Cell 9:225–238PubMedCrossRef Visentin B, Vekich JA, Sibbald BJ et al (2006) Validation of an anti-sphingosine-1-phosphate antibody as a potential therapeutic in reducing growth, invasion, and angiogenesis in multiple tumor lineages. Cancer Cell 9:225–238PubMedCrossRef
114.
go back to reference Bagnato A, Rosanò L, Spinella F et al (2004) Endothelin B receptor blockade inhibits dynamics of cell interactions and communications in melanoma cell progression. Cancer Res 64:1436–1443PubMedCrossRef Bagnato A, Rosanò L, Spinella F et al (2004) Endothelin B receptor blockade inhibits dynamics of cell interactions and communications in melanoma cell progression. Cancer Res 64:1436–1443PubMedCrossRef
115.
go back to reference Yang Y-a, Dukhanina O, Tang B et al (2002) Lifetime exposure to a soluble TGF-β antagonist protects mice against metastasis without adverse side effects. J Clin Invest 109:1607–1615PubMed Yang Y-a, Dukhanina O, Tang B et al (2002) Lifetime exposure to a soluble TGF-β antagonist protects mice against metastasis without adverse side effects. J Clin Invest 109:1607–1615PubMed
116.
go back to reference Muraoka RS, Dumont N, Ritter CA et al (2002) Blockade of TGF-ß inhibits mammary tumor cell viability, migration, and metastases. J Clin Invest 109:1551–1559PubMed Muraoka RS, Dumont N, Ritter CA et al (2002) Blockade of TGF-ß inhibits mammary tumor cell viability, migration, and metastases. J Clin Invest 109:1551–1559PubMed
117.
go back to reference Won J, Kim H, Park EJ et al (1999) Tumorigenicity of mouse thymoma is suppressed by soluble type II transforming growth factor β receptor therapy. Cancer Res 59:1273–1277PubMed Won J, Kim H, Park EJ et al (1999) Tumorigenicity of mouse thymoma is suppressed by soluble type II transforming growth factor β receptor therapy. Cancer Res 59:1273–1277PubMed
118.
go back to reference Inman GJ, Nicolás FJ, Callahan JF et al (2002) SB-431542 is a potent and specific inhibitor of transforming growth factor-β superfamily type I activin receptor-like kinase (ALK) receptors ALK4, ALK5, and ALK7. Mol Pharmacol 62:65–74PubMedCrossRef Inman GJ, Nicolás FJ, Callahan JF et al (2002) SB-431542 is a potent and specific inhibitor of transforming growth factor-β superfamily type I activin receptor-like kinase (ALK) receptors ALK4, ALK5, and ALK7. Mol Pharmacol 62:65–74PubMedCrossRef
119.
go back to reference Laping NJ, Grygielko E, Mathur A et al (2002) Inhibition of transforming growth factor (TGF)-ß1-induced extracellular matrix with a novel inhibitor of the TGF-ß type I receptor kinase activity: SB-431542. Mol Pharmacol 62:58–64PubMedCrossRef Laping NJ, Grygielko E, Mathur A et al (2002) Inhibition of transforming growth factor (TGF)-ß1-induced extracellular matrix with a novel inhibitor of the TGF-ß type I receptor kinase activity: SB-431542. Mol Pharmacol 62:58–64PubMedCrossRef
120.
go back to reference Hjelmeland MD, Hjelmeland AB, Sathornsumetee S et al (2004) SB-431542, a small molecule transforming growth factor-β-receptor antagonist, inhibits human glioma cell line proliferation and motility. Mol Cancer Ther 3:737–745PubMed Hjelmeland MD, Hjelmeland AB, Sathornsumetee S et al (2004) SB-431542, a small molecule transforming growth factor-β-receptor antagonist, inhibits human glioma cell line proliferation and motility. Mol Cancer Ther 3:737–745PubMed
121.
go back to reference Matsuyama S, Iwadate M, Kondo M et al (2003) SB-431542 and Gleevec inhibit transforming growth factor-β-induced proliferation of human osteosarcoma cells. Cancer Res 63:7791–7798PubMed Matsuyama S, Iwadate M, Kondo M et al (2003) SB-431542 and Gleevec inhibit transforming growth factor-β-induced proliferation of human osteosarcoma cells. Cancer Res 63:7791–7798PubMed
Metadata
Title
Soluble cadherins as cancer biomarkers
Authors
Olivier De Wever
Lara Derycke
An Hendrix
Gert De Meerleer
François Godeau
Herman Depypere
Marc Bracke
Publication date
01-11-2007
Publisher
Springer Netherlands
Published in
Clinical & Experimental Metastasis / Issue 8/2007
Print ISSN: 0262-0898
Electronic ISSN: 1573-7276
DOI
https://doi.org/10.1007/s10585-007-9104-8

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