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Allosteric modulators of MEK1: drug design and discovery

机译:MEK1的变构调节剂:药物设计和发现

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摘要

Mitogen-activated protein kinase kinase (MAPKK, MEK) mediates signal transduction, controlling cell proliferation and survival. MEK occupies a key downstream position in the Ras-Raf-MEK-ERK signaling pathway, implying that inhibition of MEK will potently suppress tumor cell growth, with potential applications in cancer therapy. Based on the promising therapeutic effects of MEK modulators, continued efforts have been made in this class. Here, we review the discovery and development of MEK1 allosteric modulators, classifying them into four structural groups. The allosteric mechanisms and recent clinical progress involving these modulators are also reviewed.
机译:丝裂原激活的蛋白激酶激酶(MAPKK,MEK)介导信号转导,控制细胞增殖和存活。 MEK在Ras-Raf-MEK-ERK信号传导途径中占据关键的下游位置,这表明对MEK的抑制将有效抑制肿瘤细胞的生长,在癌症治疗中具有潜在的应用前景。基于MEK调节剂的有希望的治疗作用,在此类中已经做出了持续的努力。在这里,我们审查MEK1变构调节剂的发现和发展,将其分为四个结构组。还回顾了涉及这些调节剂的变构机制和近期临床进展。

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