VEGF受体酪氨酸激酶活性选择性小分子抑制剂SU5416的研究进展。

Anti-cancer drug design Pub Date : 2000-02-01
D B Mendel, A D Laird, B D Smolich, R A Blake, C Liang, A L Hannah, R M Shaheen, L M Ellis, S Weitman, L K Shawver, J M Cherrington
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引用次数: 0

摘要

血管生成,或新血管的发芽,是实体瘤生长的核心过程。对于许多癌症,肿瘤血管化的程度是一个负面的预后指标,表明疾病的侵袭性和转移的可能性增加。最近对肿瘤相关血管生成的分子基础的研究已经确定了几个潜在的治疗靶点,包括血管生成因子血管内皮生长因子(VEGF)的受体酪氨酸激酶。在这里,我们回顾了SUGEN公司发现和开发受体酪氨酸激酶小分子抑制剂作为抗血管生成药物的方法。我们专注于SU5416,一种VEGF受体的选择性抑制剂,目前正处于临床开发阶段,用于治疗晚期恶性肿瘤。综述了其生物化学、生物学和药理学特性,并讨论了其临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of SU5416, a selective small molecule inhibitor of VEGF receptor tyrosine kinase activity, as an anti-angiogenesis agent.

Angiogenesis, or the sprouting of new blood vessels, is a central process in the growth of solid tumors. For many cancers, the extent of vascularization of a tumor is a negative prognostic indicator signifying aggressive disease and increased potential for metastasis. Recent efforts to understand the molecular basis of tumor-associated angiogenesis have identified several potential therapeutic targets, including the receptor tyrosine kinases for the angiogenic factor vascular endothelial growth factor (VEGF). Here we review the approach taken at SUGEN, Inc. to discover and develop small molecule inhibitors of receptor tyrosine kinases as anti-angiogenic agents. We focus on SU5416, a selective inhibitor of VEGF receptors that is currently in clinical development for the treatment of advanced malignancies. Its biochemical, biological and pharmacological properties are reviewed and clinical implications discussed.

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