Li Nanxin, Batt David, Warmuth Markus
Genomics Institute of the Novartis Research Foundation, Kinase Platform, 10675 John Jay Hopkins Drive, San Diego, CA 92121, USA.
Curr Opin Investig Drugs. 2007 Jun;8(6):452-6.
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.
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。