克拉斯
赫拉
神经母细胞瘤RAS病毒癌基因同源物
生物
结直肠癌
可药性
肺癌
癌症
癌症研究
癌基因
胰腺癌
生物信息学
肿瘤科
基因
遗传学
医学
细胞周期
作者
Adrienne D. Cox,Channing J. Der
标识
DOI:10.1101/gad.352081.124
摘要
The three RAS genes ( HRAS , KRAS , and NRAS ) comprise the most frequently mutated oncogene family in cancer. KRAS 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.
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