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靶向人类癌症中的RAS-RAF-MEK-ERK信号通路:临床试验现状

Targeting RAS-RAF-MEK-ERK signaling pathway in human cancer: Current status in clinical trials.

作者信息

Song Yanlin, Bi Zhenfei, Liu Yu, Qin Furong, Wei Yuquan, Wei Xiawei

机构信息

Laboratory of Aging Research and Cancer Drug Target, State Key Laboratory of Biotherapy and Cancer Center, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China.

出版信息

Genes Dis. 2022 May 20;10(1):76-88. doi: 10.1016/j.gendis.2022.05.006. eCollection 2023 Jan.

Abstract

Molecular target inhibitors have been regularly approved by Food and Drug Administration (FDA) for tumor treatment, and most of them intervene in tumor cell proliferation and metabolism. The RAS-RAF-MEK-ERK pathway is a conserved signaling pathway that plays vital roles in cell proliferation, survival, and differentiation. The aberrant activation of the RAS-RAF-MEK-ERK signaling pathway induces tumors. About 33% of tumors harbor RAS mutations, while 8% of tumors are driven by RAF mutations. Great efforts have been dedicated to targeting the signaling pathway for cancer treatment in the past decades. In this review, we summarized the development of inhibitors targeting the RAS-RAF-MEK-ERK pathway with an emphasis on those used in clinical treatment. Moreover, we discussed the potential combinations of inhibitors that target the RAS-RAF-MEK-ERK signaling pathway and other signaling pathways. The inhibitors targeting the RAS-RAF-MEK-ERK pathway have essentially modified the therapeutic strategy against various cancers and deserve more attention in the current cancer research and treatment.

摘要

分子靶向抑制剂已被美国食品药品监督管理局(FDA)常规批准用于肿瘤治疗,其中大多数抑制剂可干预肿瘤细胞的增殖和代谢。RAS-RAF-MEK-ERK信号通路是一条保守的信号通路,在细胞增殖、存活和分化中起着至关重要的作用。RAS-RAF-MEK-ERK信号通路的异常激活会诱发肿瘤。约33%的肿瘤存在RAS突变,而8%的肿瘤由RAF突变驱动。在过去几十年中,人们致力于针对该信号通路进行癌症治疗。在这篇综述中,我们总结了靶向RAS-RAF-MEK-ERK通路的抑制剂的发展情况,重点介绍了用于临床治疗的抑制剂。此外,我们还讨论了靶向RAS-RAF-MEK-ERK信号通路的抑制剂与其他信号通路的潜在联合应用。靶向RAS-RAF-MEK-ERK通路的抑制剂已从根本上改变了针对各种癌症的治疗策略,在当前的癌症研究和治疗中值得更多关注。

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