Department of Gynecologic Oncology & Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Gynecologic Oncology & Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA; The University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, TX, USA.
Cancer Treat Rev. 2021 Jan;92:102137. doi: 10.1016/j.ctrv.2020.102137. Epub 2020 Dec 16.
The mitogen-activated protein kinase (MAPK) pathway plays a vital role in cellular processes such as gene expression, cell proliferation, cell survival, and apoptosis. Also known as the RAS-RAF-MEK-ERK pathway, the MAPK pathway has been implicated in approximately one-third of all cancers. Mutations in RAS or RAF genes such as KRAS and BRAF are common, and these mutations typically promote malignancies by over-activating MEK and ERK downstream, which drives sustained cell proliferation and uninhibited cell growth. Development of drugs targeting this pathway has been a research area of great interest, especially drugs targeting the inhibition of MEK. In vitro and clinical studies have shown promise for certain MEK inhibitors (MEKi) , and MEKi have become the first treatment option for certain cancers. Despite promising results, not all patients have a response to MEKi, and mechanisms of resistance typically arise in patients who do have a positive initial response. This paper summarizes recent developments regarding MEKi, the mechanisms of adaptive resistance to MEKi, and the potential solutions to the issue of adaptive MEKi resistance.
丝裂原活化蛋白激酶(MAPK)通路在细胞过程中发挥着重要作用,如基因表达、细胞增殖、细胞存活和细胞凋亡。MAPK 通路也被称为 RAS-RAF-MEK-ERK 通路,大约三分之一的癌症都与该通路有关。RAS 或 RAF 基因(如 KRAS 和 BRAF)的突变很常见,这些突变通常通过过度激活 MEK 和 ERK 下游来促进恶性肿瘤,从而导致持续的细胞增殖和不受抑制的细胞生长。针对该通路的药物开发一直是一个非常感兴趣的研究领域,特别是针对 MEK 抑制的药物。体外和临床研究表明某些 MEK 抑制剂(MEKi)有一定的应用前景,并且 MEKi 已经成为某些癌症的首选治疗方法。尽管有令人鼓舞的结果,但并非所有患者对 MEKi 都有反应,并且在最初反应阳性的患者中,耐药机制通常会出现。本文总结了 MEKi 的最新进展、对 MEKi 的适应性耐药机制,以及解决适应性 MEKi 耐药问题的潜在方法。