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新型丝裂原活化蛋白激酶激酶抑制剂。

Novel mitogen-activated protein kinase kinase inhibitors.

机构信息

Biogen Idec, San Diego, California, USA

出版信息

Expert Opin Investig Drugs. 2011 Feb;20(2):209-20. doi: 10.1517/13543784.2011.548803.

Abstract

INTRODUCTION

the development of new drugs over the last few decades has targeted specific proteins thought to be a key to the disease state. MAPK kinases 1 and 2 (commonly known as MEK1-2) represent such proteins as they lie downstream of important drug targets for oncology, such as EGFR, RAS and RAF. Several MEK1-2 inhibitors are currently in Phase I and II clinical trials in oncology.

AREAS COVERED

this review of current literature and recent conferences provides a background on the RAS-RAF-MEK-ERK signaling pathway and a discussion of early MEK inhibitors. The potential of MEK1-2 inhibitors for the treatment of inflammation is briefly presented. Preclinical and early clinical results are discussed for MEK inhibitors currently in development. Completed clinical trials of MEK inhibitors in oncology include some disappointments as well as some promising signs of the value of these compounds and we discuss the potential for MEK inhibitors as monotherapy and their use in drug combinations.

EXPERT OPINION

the utility of MEK inhibitors as anticancer agents will depend on careful patient selection based on the presence of mutations in genes such as KRAS and BRAF, the identification of additional predictive biomarkers, and an improved understanding of the benefit of drug combinations utilizing both established and emerging therapeutics.

摘要

简介

过去几十年里开发的新药针对的是被认为是疾病状态关键的特定蛋白质。丝裂原活化蛋白激酶激酶 1 和 2(通常称为 MEK1-2)就是这样的蛋白质,因为它们位于肿瘤学的重要药物靶点 EGFR、RAS 和 RAF 的下游。目前有几种 MEK1-2 抑制剂正在肿瘤学的 I 期和 II 期临床试验中。

涵盖领域

本文对当前文献和最近会议进行综述,为 RAS-RAF-MEK-ERK 信号通路提供背景知识,并讨论早期 MEK 抑制剂。简要介绍了 MEK1-2 抑制剂治疗炎症的潜力。讨论了目前正在开发的 MEK 抑制剂的临床前和早期临床结果。已完成的肿瘤学中 MEK 抑制剂临床试验既有一些令人失望的结果,也有一些有前途的迹象表明这些化合物具有价值,我们讨论了 MEK 抑制剂作为单一疗法的潜力及其在药物联合治疗中的应用。

专家意见

MEK 抑制剂作为抗癌药物的效用将取决于根据 KRAS 和 BRAF 等基因的突变、识别其他预测性生物标志物以及更好地了解利用现有和新兴疗法的药物联合治疗的益处来进行仔细的患者选择。

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