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Published in: Investigational New Drugs 2/2012

01-04-2012 | PRECLINICAL STUDIES

New Vandetanib analogs: fused tricyclic quinazolines with antiangiogenic potential

Authors: Maria Teresa Conconi, Giovanni Marzaro, Adriano Guiotto, Luca Urbani, Ilenia Zanusso, Francesca Tonus, Mara Tommasini, Pier Paolo Parnigotto, Adriana Chilin

Published in: Investigational New Drugs | Issue 2/2012

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Summary

The antiangiogenic effects of three novel anilinoquinazoline derivatives were studied with the aim to find new multi-kinase inhibitors as anticancer agents. The compounds are characterized by dioxolane, dioxane and dioxepine rings and bear the same aniline substituent in 4 position as Vandetanib, known antiangiogenic agent. The in vitro assays were carried out on human umbilical vein endothelial cells (HUVECs), whereas in vivo angiogenesis was evaluated by means of Matrigel plug assay. The results showed that these compounds exert, even though to different extents, antiangiogenic activity affecting the various step of the process that leads to the formation of new blood vessels. At high concentrations they induced antiproliferative effects, whereas at non-cytotoxic concentrations they inhibited cell migration and the formation of tubular structures in Matrigel. In in vitro assays the dioxolane derivative 1 was more effective than Vandetanib. Indeed, it inhibited the effects induced by exogenous VEGF and FGF-2 on both cell proliferation and morphogenesis, whereas Vandetanib was completely ineffective. Moreover, all the compounds, as Vandetanib, counteracted the FGF-2-induced increase in the hemoglobin content in the Matrigel plugs. Our results showed that all the three novel derivatives possess both in vitro and in vivo antiangiogenic activity, with compound 1 more effective than Vandetanib to inhibit in vitro angiogenesis induced by exogenous cytokines.
Literature
1.
go back to reference Bazley LA, Gullick WJ (2005) The epidermal growth factor receptor family. Endocr-Relat Cancer 12(Suppl 1):S17–S27PubMedCrossRef Bazley LA, Gullick WJ (2005) The epidermal growth factor receptor family. Endocr-Relat Cancer 12(Suppl 1):S17–S27PubMedCrossRef
2.
go back to reference Citri A, Yarden Y (2006) EGF-ERBB signalling: towards the systems level. Nat Rev 7(7):505–516CrossRef Citri A, Yarden Y (2006) EGF-ERBB signalling: towards the systems level. Nat Rev 7(7):505–516CrossRef
3.
go back to reference Takeuchi K, Ito F (2010) EGF receptor in relation to tumor development: molecular basis of responsiveness of cancer cells to EGFR-targeting tyrosine kinase inhibitors. FEBS J 277(2):316–326PubMedCrossRef Takeuchi K, Ito F (2010) EGF receptor in relation to tumor development: molecular basis of responsiveness of cancer cells to EGFR-targeting tyrosine kinase inhibitors. FEBS J 277(2):316–326PubMedCrossRef
4.
go back to reference Ferrara N, Gerber HP, LeCouter J (2003) The biology of VEGF and its receptors. Nat Med 9(6):669–676PubMedCrossRef Ferrara N, Gerber HP, LeCouter J (2003) The biology of VEGF and its receptors. Nat Med 9(6):669–676PubMedCrossRef
5.
go back to reference Przybylski M (2009) A review of the current research on the role of bFGF and VEGF in angiogenesis. J Wound Care 18(12):516–519PubMed Przybylski M (2009) A review of the current research on the role of bFGF and VEGF in angiogenesis. J Wound Care 18(12):516–519PubMed
6.
go back to reference Folkman J (2007) Angiogenesis: an organizing principle for drug discovery? Nat Rev Drug Discov 6(4):273–286PubMedCrossRef Folkman J (2007) Angiogenesis: an organizing principle for drug discovery? Nat Rev Drug Discov 6(4):273–286PubMedCrossRef
7.
go back to reference Tabernero J (2007) The role of VEGF and EGFR inhibition: implications for combining anti-VEGF and anti-EGFR agents. Mol Cancer Res 5(3):203–220PubMedCrossRef Tabernero J (2007) The role of VEGF and EGFR inhibition: implications for combining anti-VEGF and anti-EGFR agents. Mol Cancer Res 5(3):203–220PubMedCrossRef
8.
go back to reference Ellis LM (2004) Epidermal growth factor receptor in tumor angiogenesis. Hematol Oncol Clin North Am 18(5):1007–1021, viiiPubMedCrossRef Ellis LM (2004) Epidermal growth factor receptor in tumor angiogenesis. Hematol Oncol Clin North Am 18(5):1007–1021, viiiPubMedCrossRef
9.
go back to reference Birk DM, Barbato J, Mureebe L, Chaer RA (2008) Current insights on the biology and clinical aspects of VEGF regulation. Vasc Endovasc Surg 42(6):517–530CrossRef Birk DM, Barbato J, Mureebe L, Chaer RA (2008) Current insights on the biology and clinical aspects of VEGF regulation. Vasc Endovasc Surg 42(6):517–530CrossRef
10.
go back to reference Ryan AJ, Wedge SR (2005) ZD6474–a novel inhibitor of VEGFR and EGFR tyrosine kinase activity. Br J Cancer 92(Suppl 1):S6–S13PubMedCrossRef Ryan AJ, Wedge SR (2005) ZD6474–a novel inhibitor of VEGFR and EGFR tyrosine kinase activity. Br J Cancer 92(Suppl 1):S6–S13PubMedCrossRef
11.
go back to reference Chilin A, Conconi MT, Marzaro G, Guiotto A, Urbani L, Tonus F, Parnigotto P (2010) Exploring epidermal growth factor receptor (EGFR) inhibitor features: the role of fused dioxygenated rings on the quinazoline scaffold. J Med Chem 53(4):1862–1866PubMedCrossRef Chilin A, Conconi MT, Marzaro G, Guiotto A, Urbani L, Tonus F, Parnigotto P (2010) Exploring epidermal growth factor receptor (EGFR) inhibitor features: the role of fused dioxygenated rings on the quinazoline scaffold. J Med Chem 53(4):1862–1866PubMedCrossRef
12.
go back to reference Marzaro G, Guiotto A, Pastorini G, Chilin A (2010) A novel approach to quinazolin-4(3H)-one via quinazoline oxidation: an improved synthesis of 4-anilinoquinazolines. Tetrahedron 66(4):962–968CrossRef Marzaro G, Guiotto A, Pastorini G, Chilin A (2010) A novel approach to quinazolin-4(3H)-one via quinazoline oxidation: an improved synthesis of 4-anilinoquinazolines. Tetrahedron 66(4):962–968CrossRef
13.
go back to reference Fry DW (2003) Mechanism of action of erbB tyrosine kinase inhibitors. Exp Cell Res 284(1):131–139PubMedCrossRef Fry DW (2003) Mechanism of action of erbB tyrosine kinase inhibitors. Exp Cell Res 284(1):131–139PubMedCrossRef
14.
go back to reference Soares R, Guo S, Gartner F, Schmitt FC, Russo J (2003) 17 beta -estradiol-mediated vessel assembly and stabilization in tumor angiogenesis requires TGF beta and EGFR crosstalk. Angiogenesis 6(4):271–281PubMedCrossRef Soares R, Guo S, Gartner F, Schmitt FC, Russo J (2003) 17 beta -estradiol-mediated vessel assembly and stabilization in tumor angiogenesis requires TGF beta and EGFR crosstalk. Angiogenesis 6(4):271–281PubMedCrossRef
15.
go back to reference Jane EP, Premkumar DR, Addo-Yobo SO, Pollack IF (2009) Abrogation of mitogen-activated protein kinase and Akt signaling by vandetanib synergistically potentiates histone deacetylase inhibitor-induced apoptosis in human glioma cells. J Pharmacol Exp Ther 331(1):327–337PubMedCrossRef Jane EP, Premkumar DR, Addo-Yobo SO, Pollack IF (2009) Abrogation of mitogen-activated protein kinase and Akt signaling by vandetanib synergistically potentiates histone deacetylase inhibitor-induced apoptosis in human glioma cells. J Pharmacol Exp Ther 331(1):327–337PubMedCrossRef
16.
go back to reference Jia HY, Wu JX, Zhu XF, Chen JM, Yang SP, Yan HJ, Tan L, Zeng YX, Huang W (2009) ZD6474 inhibits Src kinase leading to apoptosis of imatinib-resistant K562 cells. Leuk Res 33(11):1512–1519PubMedCrossRef Jia HY, Wu JX, Zhu XF, Chen JM, Yang SP, Yan HJ, Tan L, Zeng YX, Huang W (2009) ZD6474 inhibits Src kinase leading to apoptosis of imatinib-resistant K562 cells. Leuk Res 33(11):1512–1519PubMedCrossRef
17.
go back to reference Munoz-Chapuli R, Quesada AR, Angel Medina M (2004) Angiogenesis and signal transduction in endothelial cells. Cell Mol Life Sci 61(17):2224–2243PubMedCrossRef Munoz-Chapuli R, Quesada AR, Angel Medina M (2004) Angiogenesis and signal transduction in endothelial cells. Cell Mol Life Sci 61(17):2224–2243PubMedCrossRef
18.
go back to reference van Wetering S, van den Berk N, van Buul JD, Mul FP, Lommerse I, Mous R, ten Klooster JP, Zwaginga JJ, Hordijk PL (2003) VCAM-1-mediated Rac signaling controls endothelial cell-cell contacts and leukocyte transmigration. Am J Physiol 285(2):C343–C352 van Wetering S, van den Berk N, van Buul JD, Mul FP, Lommerse I, Mous R, ten Klooster JP, Zwaginga JJ, Hordijk PL (2003) VCAM-1-mediated Rac signaling controls endothelial cell-cell contacts and leukocyte transmigration. Am J Physiol 285(2):C343–C352
19.
go back to reference Gerety SS, Wang HU, Chen ZF, Anderson DJ (1999) Symmetrical mutant phenotypes of the receptor EphB4 and its specific transmembrane ligand ephrin-B2 in cardiovascular development. Mol Cell 4(3):403–414PubMedCrossRef Gerety SS, Wang HU, Chen ZF, Anderson DJ (1999) Symmetrical mutant phenotypes of the receptor EphB4 and its specific transmembrane ligand ephrin-B2 in cardiovascular development. Mol Cell 4(3):403–414PubMedCrossRef
20.
go back to reference Ogino H, Yano S, Kakiuchi S, Yamada T, Ikuta K, Nakataki E, Goto H, Hanibuchi M, Nishioka Y, Ryan A, Sone S (2008) Novel dual targeting strategy with vandetanib induces tumor cell apoptosis and inhibits angiogenesis in malignant pleural mesothelioma cells expressing RET oncogenic rearrangement. Cancer Lett 265(1):55–66PubMedCrossRef Ogino H, Yano S, Kakiuchi S, Yamada T, Ikuta K, Nakataki E, Goto H, Hanibuchi M, Nishioka Y, Ryan A, Sone S (2008) Novel dual targeting strategy with vandetanib induces tumor cell apoptosis and inhibits angiogenesis in malignant pleural mesothelioma cells expressing RET oncogenic rearrangement. Cancer Lett 265(1):55–66PubMedCrossRef
21.
go back to reference Lyros O, Mueller A, Heidel F, Schimanski CC, Gockel I, Galle PR, Lang H, Moehler M (2010) Analysis of anti-proliferative and chemosensitizing effects of sunitinib on human esophagogastric cancer cells: synergistic interaction with vandetanib via inhibition of multi-receptor tyrosine kinase pathways. Int J Cancer 127(5):1197–1208PubMedCrossRef Lyros O, Mueller A, Heidel F, Schimanski CC, Gockel I, Galle PR, Lang H, Moehler M (2010) Analysis of anti-proliferative and chemosensitizing effects of sunitinib on human esophagogastric cancer cells: synergistic interaction with vandetanib via inhibition of multi-receptor tyrosine kinase pathways. Int J Cancer 127(5):1197–1208PubMedCrossRef
Metadata
Title
New Vandetanib analogs: fused tricyclic quinazolines with antiangiogenic potential
Authors
Maria Teresa Conconi
Giovanni Marzaro
Adriano Guiotto
Luca Urbani
Ilenia Zanusso
Francesca Tonus
Mara Tommasini
Pier Paolo Parnigotto
Adriana Chilin
Publication date
01-04-2012
Publisher
Springer US
Published in
Investigational New Drugs / Issue 2/2012
Print ISSN: 0167-6997
Electronic ISSN: 1573-0646
DOI
https://doi.org/10.1007/s10637-010-9621-1

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