Department of Clinical Biochemistry, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad,Iran.
Medical Plants Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord,Iran.
Curr Cancer Drug Targets. 2021;21(11):932-943. doi: 10.2174/1568009621666211103113339.
The MAPK/ERK signaling pathway regulates cancer cell proliferation, apoptosis, inflammation, angiogenesis, metastasis and drug resistance. Mutations and up-regulation of components of the MAPK/ERK signaling pathway, as well as over-activation of this critical signaling pathway, are frequently observed in colorectal carcinomas. Targeting the MAPK/ERK signaling pathway, using specific pharmacological inhibitors, elicits potent anti-tumor effects, supporting the therapeutic potential of these inhibitors in the treatment of CRC. Several drugs have recently been developed for the inhibition of the MEK/ERK pathway in preclinical and clinical settings, such as MEK162 and MK-2206. MEK1/2 inhibitors demonstrate promising efficacy and anticancer activity for the treatment of this malignancy. This review summarizes the current knowledge on the role of the MAPK/ERK signaling pathway in the pathogenesis of CRC and the potential clinical value of synthetic inhibitors of this pathway in preventing CRC progression for a better understanding, and hence, better management of colorectal cancer.
MAPK/ERK 信号通路调节癌细胞的增殖、凋亡、炎症、血管生成、转移和耐药性。在结直肠癌中,经常观察到 MAPK/ERK 信号通路的组成部分发生突变和上调,以及该关键信号通路的过度激活。使用特定的药理抑制剂靶向 MAPK/ERK 信号通路,可产生强大的抗肿瘤作用,支持这些抑制剂在 CRC 治疗中的治疗潜力。近年来,已有几种药物在临床前和临床环境中被开发用于抑制 MEK/ERK 通路,如 MEK162 和 MK-2206。MEK1/2 抑制剂在治疗这种恶性肿瘤方面表现出有希望的疗效和抗癌活性。本文综述了 MAPK/ERK 信号通路在 CRC 发病机制中的作用以及该通路合成抑制剂在预防 CRC 进展中的潜在临床价值,以更好地理解并因此更好地管理结直肠癌。