Recent developments in the inhibition of angiogenesis: examples from studies on platelet factor-4 and the VEGF/VEGFR system |
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Authors: | Bikfalvi Andreas |
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Affiliation: | Molecular Mechanisms of Angiogenesis Laboratory (INSERM E0113), Université Bordeaux I, Avenue des Facultés, 33 405 Talence, France. a.bikfalvi@angio.u-bordeaux1.fr |
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Abstract: | Inhibition of angiogenesis is an important strategy to block tumor growth and invasion. We discuss herein results from our ongoing investigations on platelet factor-4 (PF-4) and the VEGF/VEGFR system. Platelet factor-4 (PF-4) is an anti-angiogenic ELR-negative chemokine. PF-4 inhibits endothelial cell proliferation and migration, and angiogenesis in vitro and in vivo. We have studied the structure and anti-angiogenic activities of a C-terminal fragment of PF-4 named PF-4 CTF. This molecule retains anti-angiogenic activity, blocks the interaction of angiogenesis factors with their receptors and may also be improved by mutation or domain-swapping. It seems, therefore, to be a good candidate for further development. Furthermore, we have developed a cyclic vascular endothelial growth inhibitor (Cyclo VEGI) from the structure of VEGF-A. In aqueous solution, cyclo-VEGI adopts an alpha helix conformation. Cyclo-VEGI inhibits binding of iodinated VEGF(165) to endothelial cells and angiogenesis. Furthermore, cyclo-VEGI significantly blocks the growth of established intracranial glioma in nude and syngeneic mice and improves survival. |
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Keywords: | BCE, bovine capillary endothelial cells cyclo-VEGI, cyclic vascular endothelial growth inhibitor CXCR3-B, CXC chemokine receptor 3 variant B FGF, fibroblast growth factor HSPGs, heparan sulfate proteoglycans HUVEC, human umbilical vein endothelial cell PF-4, platelet factor-4 VEGF, vascular endothelial growth factor |
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