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用于癌症治疗的B-Raf激酶抑制剂。

B-Raf kinase inhibitors for cancer treatment.

作者信息

Li Nanxin, Batt David, Warmuth Markus

机构信息

Genomics Institute of the Novartis Research Foundation, Kinase Platform, 10675 John Jay Hopkins Drive, San Diego, CA 92121, USA.

出版信息

Curr Opin Investig Drugs. 2007 Jun;8(6):452-6.

Abstract

The Raf-MEK-ERK signaling pathway is critical for cell survival, growth, proliferation and tumorigenesis. Among the three isoforms of Raf protein kinases, in vitro and in vivo studies have shown that B-Raf functions as the primary MEK activator. B-Raf is one of the most frequently mutated genes in human cancers with a high prevalence in melanoma, and many of the B-Raf mutations activate the kinase activity of B-Raf. B-Raf kinase represents an excellent target for anticancer therapy based on preclinical target validation, epidemiology and drugability. Several small-molecule inhibitors of B-Raf kinase are currently undergoing clinical evaluation, with others due to enter clinical development in the near future.

摘要

Raf-MEK-ERK信号通路对细胞存活、生长、增殖和肿瘤发生至关重要。在Raf蛋白激酶的三种同工型中,体外和体内研究表明,B-Raf作为主要的MEK激活剂发挥作用。B-Raf是人类癌症中最常发生突变的基因之一,在黑色素瘤中具有很高的发生率,并且许多B-Raf突变激活了B-Raf的激酶活性。基于临床前靶点验证、流行病学和药物可及性,B-Raf激酶是抗癌治疗的一个极佳靶点。目前有几种B-Raf激酶的小分子抑制剂正在进行临床评估,其他一些抑制剂也将在不久的将来进入临床开发阶段。

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