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“不可成药的KRAS”:终究是可成药的。

"Undruggable KRAS": druggable after all.

作者信息

Cox Adrienne D, Der Channing J

机构信息

Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA;

Department of Radiation Oncology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.

出版信息

Genes Dev. 2025 Jan 7;39(1-2):132-162. doi: 10.1101/gad.352081.124.

Abstract

The three genes (, , and ) comprise the most frequently mutated oncogene family in cancer. is the predominant isoform mutated in cancer and is most prevalently mutated in major causes of cancer deaths including lung, colorectal, and pancreatic cancers. Despite extensive academic and industry efforts to target KRAS, it would take nearly four decades before approval of the first clinically effective KRAS inhibitors for the treatment of KRAS mutant lung cancer. We revisit past anti-KRAS strategies and painful lessons learned and then focus on the rapidly evolving landscape of direct RAS inhibitors, resistance mechanisms, and potential combination treatments.

摘要

这三个基因( 、 和 )构成了癌症中最常发生突变的癌基因家族。 是癌症中突变的主要异构体,在包括肺癌、结直肠癌和胰腺癌在内的主要癌症死亡原因中突变最为普遍。尽管学术界和业界为靶向KRAS付出了巨大努力,但在首个治疗KRAS突变型肺癌的临床有效KRAS抑制剂获批之前,仍花费了近四十年时间。我们回顾过去的抗KRAS策略以及吸取的惨痛教训,然后重点关注直接RAS抑制剂、耐药机制和潜在联合治疗快速发展的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1e9/11789494/3efdc06dc274/132f02.jpg

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