4.7 Review

MEK in cancer and cancer therapy

期刊

PHARMACOLOGY & THERAPEUTICS
卷 141, 期 2, 页码 160-171

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pharmthera.2013.10.001

关键词

MAP kinases; ERK inhibitors; Targeted therapy; Resistance; Predictive biomarker; Combination

资金

  1. Foundation Nelia & Amadeo Barleta (FNAB)
  2. Association pour l'Aide a la Recherche & l'Enseignement en Cancerologie (AAREC)

向作者/读者索取更多资源

The mitogen-activated extracellular signal-regulated kinase (MEK) pathway is one of the best-characterized kinase cascades in cancer cell biology. It is triggered by either growth factors or activating mutations of major oncogenic proteins in this pathway, the most common being Ras and Raf. Deregulation of this pathway is frequently observed and plays a central role in the carcinogenesis and maintenance of several cancers, including melanoma, pancreatic, lung, colorectal, and breast cancers. Targeting these kinases offers promise of novel therapies. MEK inhibitors (MEKi) are currently under evaluation in clinical trials and many have shown activity. In this review, we comprehensively examine the role of the MEK pathway in carcinogenesis and its therapeutic potential in cancer patients, with a focus on MEKi. We describe the clinical perspectives of MEKi in the two main models of Ras-ERK driven tumors, BRAF-mutant (addicted to the pathway) and KRAS-mutant (non-addicted). We also highlight the known mechanisms of resistance to MEKi and emerging strategies to overcome it. (C) 2013 Elsevier Inc All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据