Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Portugal.
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Portugal.
Drug Discov Today. 2016 Oct;21(10):1654-1663. doi: 10.1016/j.drudis.2016.06.010. Epub 2016 Jun 16.
Conventional mitogen-activated protein kinase (MAPK) family members are among the most sought-after oncogenic effectors for the development of novel human cancer treatment strategies. MEK5/ERK5 has been the less-studied MAPK subfamily, despite its increasingly demonstrated relevance in the growth, survival, and differentiation of normal cells. MEK5/ERK5 signalling has already been proposed to have pivotal roles in several cancer hallmarks, and to mediate the effects of a range of oncogenes. Accumulating evidence indicates the contribution of MEK5/ERK5 signalling to therapy resistance and the benefits of using MEK5/ERK5 inhibitory strategies in the treatment of human cancer. Here, we explore the major known contributions of MEK5/ERK5 signalling to the onset and progression of several types of cancer, and highlight the potential clinical relevance of targeting MEK5/ERK5 pathways.
传统的丝裂原活化蛋白激酶(MAPK)家族成员是开发新型人类癌症治疗策略中最受关注的致癌效应物之一。MEK5/ERK5 是研究较少的 MAPK 亚家族,尽管其在正常细胞的生长、存活和分化中的相关性越来越明显。MEK5/ERK5 信号已经被提出在多种癌症特征中具有关键作用,并介导一系列癌基因的作用。越来越多的证据表明 MEK5/ERK5 信号对治疗耐药性的贡献,以及使用 MEK5/ERK5 抑制策略治疗人类癌症的益处。在这里,我们探讨了 MEK5/ERK5 信号对几种类型癌症的发生和进展的主要已知贡献,并强调了靶向 MEK5/ERK5 途径的潜在临床相关性。