血管生成
贝伐单抗
医学
血管内皮生长因子
癌症研究
新生血管
伤口愈合
癌症
血管内皮生长因子A
内皮干细胞
免疫学
血管内皮生长因子受体
内科学
病理
化疗
生物
体外
生物化学
标识
DOI:10.1016/s0093-7754(02)70064-x
摘要
Angiogenesis, or formation of new blood vessels from pre-existing ones, is essential for normal development and wound healing/reproductive functions in adults. Abnormal regulation of angiogenesis has been implicated in the pathogenesis of several disorders, including cancer. Vascular endothelial growth factor (VEGF)-A is a pivotal stimulator of angiogenesis because its binding to VEGF receptors has been shown to promote endothelial cell migration and proliferation, two key features required for the development of new blood vessels. In addition, VEGF-A increases vascular permeability, which may also contribute to angiogenesis and tumor growth. Recognition of the central role of VEGF-A in angiogenesis has led to the hypothesis that its inhibition may represent a novel and effective approach to the treatment of cancer and other conditions characterized by pathologic angiogenesis. Several lines of evidence support this idea, and early clinical experience with the humanized anti-VEGF–A monoclonal antibody bevacizumab (Avastin, rhuMAb-VEGF; Genentech, South San Francisco, CA) has been encouraging. Clinical efficacy of antiangiogenic therapy with bevacizumab is being evaluated in several phase 3 trials in various types of cancer, as well as in patients with age-related macular degeneration. Semin Oncol 29 (suppl 16):10-14. Copyright 2002, Elsevier Science (USA). All rights reserved.
科研通智能强力驱动
Strongly Powered by AbleSci AI