Mendel D B, Laird A D, Smolich B D, Blake R A, Liang C, Hannah A L, Shaheen R M, Ellis L M, Weitman S, Shawver L K, Cherrington J M
SUGEN, Inc., South San Francisco, CA 94080, USA.
Anticancer Drug Des. 2000 Feb;15(1):29-41.
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.
血管生成,即新血管的萌发,是实体瘤生长的核心过程。对于许多癌症来说,肿瘤血管化程度是一个负面预后指标,意味着疾病具有侵袭性且转移可能性增加。最近为了解肿瘤相关血管生成的分子基础所做的努力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公司为发现和开发作为抗血管生成药物的受体酪氨酸激酶小分子抑制剂所采取的方法。我们重点关注SU5416,一种VEGF受体的选择性抑制剂,目前正处于治疗晚期恶性肿瘤的临床开发阶段。本文对其生化、生物学和药理学特性进行了综述,并讨论了其临床意义。