Napoleone Ferrara和血管内皮生长因子的传奇。

Domenico Ribatti
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引用次数: 14

摘要

1989年,基因泰克公司的Napoleone Ferrara和他的同事首次分离并克隆了血管内皮生长因子(VEGF)。他的实验室研究了VEGF生物化学和分子生物学的许多方面。1993年,Ferrara报道了特异性单克隆抗体抑制vegf诱导的血管生成,可显著抑制体内多种肿瘤的生长。这些发现为抑制血管生成可能抑制肿瘤生长和阻断VEGF作用对多种恶性肿瘤具有治疗价值提供了重要证据,并验证了Judah Folkman在1971年提出的抑制肿瘤血管生成可能是控制肿瘤生长的有效方法的观点。进一步的发展是在1997年以合理的方式设计了一种人源化抗vegf单克隆抗体(Avastin),现在在临床试验中作为几种实体瘤的治疗方法,也用于癌症以外的治疗,例如,用于治疗年龄相关性黄斑变性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Napoleone Ferrara and the saga of vascular endothelial growth factor.

Napoleone Ferrara and his colleagues at Genentech were the first to isolate and clone vascular endothelial growth factor (VEGF) in 1989. His laboratory has investigated many aspects of VEGF biochemistry and molecular biology. In 1993, Ferrara reported that inhibition of VEGF-induced angiogenesis by specific monoclonal antibodies resulted in dramatic suppression of the growth of a variety of tumors in vivo. These findings provided an important evidence that inhibition of angiogenesis may suppress tumor growth and blocking VEGF action could have therapeutic value for a variety of malignancies and validate the notion introduced in 1971 by Judah Folkman that inhibition of tumor angiogenesis might be a valid approach to control tumor growth. A further development was the design in a rational fashion in 1997 of a humanized anti-VEGF monoclonal antibody (Avastin), now in clinical trials as a treatment for several solid tumors and also outside of cancer, for example, in the treatment of age-related macular degeneration.

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