RAS抑制剂:潜在的癌症治疗药物

Yoel Kloog PhD (Professor of Biochemistry) , Adrienne D Cox PhD (Assistant Professor)
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引用次数: 87

摘要

由于RAS癌蛋白在人类恶性肿瘤中发挥重要作用,抑制RAS功能是开发抗癌治疗的一种很有前景的方法。这些方法包括法尼基转移酶抑制剂(FTIs)和无毒性法尼基半胱氨酸类似物法尼基硫代水杨酸(FTS)等药物,它们可以将所有RAS亚型从膜上移除,以及恢复RAS - gtp水平的调节和改变RAS - gtp与下游靶点的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RAS inhibitors: potential for cancer therapeutics

As RAS oncoproteins play a major role in human malignancy, inhibiting RAS function is a promising approach for developing anticancer therapies. Among these approaches are agents such as farnesyltransferase inhibitors (FTIs) and the nontoxic farnesylcysteine analogue farnesylthiosalicylic acid (FTS) that dislodges all RAS isoforms from the membrane, as well as methods to restore regulation of RAS–GTP levels and to alter the interaction of RAS–GTP with downstream targets.

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