Friday Bret B, Adjei Alex A
Department of Oncology, Mayo Clinic, Rochester, MN, USA.
Clin Cancer Res. 2008 Jan 15;14(2):342-6. doi: 10.1158/1078-0432.CCR-07-4790.
The identification of intracellular signaling cascades important for the growth and survival of cancer cells has led to the development of targeted cancer therapeutics aimed at blocking these signals. The mitogen-activated protein kinase (MAPK) pathway has a well-defined role in cancer biology and has been an important target in the development of targeted therapies. Recently, several small-molecule inhibitors of MAPK/extracellular signal-regulated kinase kinase (MEK), a key intermediary of MAPK signaling, have been developed and are currently being tested in clinical trials. Herein, we review the MAPK pathway, the development of small-molecule MEK inhibitors, and the results obtained to date with MEK inhibitors in human cancer trials.
对癌细胞生长和存活至关重要的细胞内信号级联的识别,促使了旨在阻断这些信号的靶向癌症治疗方法的发展。丝裂原活化蛋白激酶(MAPK)通路在癌症生物学中具有明确的作用,并且一直是靶向治疗开发中的重要靶点。最近,几种丝裂原活化蛋白激酶/细胞外信号调节激酶激酶(MEK)的小分子抑制剂已被开发出来,目前正在临床试验中进行测试。在此,我们综述了MAPK通路、小分子MEK抑制剂的开发以及迄今为止在人类癌症试验中使用MEK抑制剂所获得的结果。