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KRAS 抑制剂——是的,但下一步是什么?直接靶向 KRAS——疫苗、过继性 T 细胞疗法及更多

英文原题:KRAS Inhibitors- yes but what next? Direct targeting of KRAS- vaccines, adoptive T cell therapy and beyond.

PubMed 2021/10/21(内容时间) Cancer Treat Rev Q1 · IF 10.6(JCR 2025)

研究概要

Kirsten大鼠肉瘤病毒癌基因同源物(KRAS)是RAS-MAPK通路的原癌基因。

中文摘要

Kirsten大鼠肉瘤病毒癌基因同源物(KRAS)是RAS-MAPK通路的原癌基因。KRAS突变存在于多种恶性肿瘤中,包括肺癌、结直肠癌和胰腺癌。在KRAS G12C抑制剂sotorasib近期获批之前,KRAS缺乏靶向治疗导致携带KRAS突变肿瘤的患者预后较差。虽然sotorasib的条件性批准对携带KRAS G12C突变的患者而言是一项重大突破,但G12C仅占KRAS突变患者的一小部分,且对G12C抑制剂的最终耐药不可避免。这篇关于KRAS抑制剂的综合性综述涵盖了不断积累的证据,不仅涉及G12C抑制剂,还涉及其他针对KRAS的治疗尝试,包括联合治疗以及疫苗、过继性T细胞疗法、蛋白水解靶向嵌合体(PROTAC)和CRISPR/Cas9的直接抑制。

展开英文摘要原文

Kirsten rat sarcoma viral oncogene homolog (KRAS) is a proto-oncogene of the RAS-MAPK pathway. KRAS mutations are present in a variety of malignancies including lung, colorectal, and pancreatic cancer. Until the recent approval of sotorasib, a KRAS G12C inhibitor, lack of targeted therapy for KRAS has resulted in poor prognosis of patients with tumors harboring KRAS mutations. While the conditional approval of sotorasib was a major breakthrough for those patients harboring KRAS G12C mutations, G12C only accounts for a fraction of those with KRAS mutations and eventual resistance to G12C inhibitors are unavoidable. This comprehensive review on KRAS inhibitors covers accumulating evidence on not only the G12C inhibitors but also other therapeutic attempts to tackle KRAS including combination therapy as well as direct inhibition with vaccines, adoptive T cell therapy, proteolysis-targeted chimeras (PROTACs) and CRISPR/Cas9.

论文信息

作者
Nagasaka M、Potugari B、Nguyen A、Sukari A、Azmi AS、Ou SI
单位
University of California Irvine School of Medicine, Orange, CA, USA; Chao Family Comprehensive Cancer Center, Orange, CA, USA; Division of Neurology, Department of Internal Medicine, St. Marianna University, Kawasaki, Japan. Electronic address: nagasakm@hs.uci.edu.United States
文献类型
综述
期刊
Cancer treatment reviews2021 Dec
原文标识
PubMed 34715449 · DOI 10.1016/j.ctrv.2021.102309