Suppr超能文献

靶向结直肠癌中的KRAS(综述)。

Targeting KRAS in colorectal cancer (Review).

作者信息

Zhang Minjie, Wu Dawei, Tang Yu, Zhang Li, Zhang Shuquan, Li Wei, Li Ning, Yan Xinhua

机构信息

Clinical Trials Center, Luanzhou People's Hospital, Tangshan, Hebei 063700, P.R. China.

Clinical Trials Center, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, P.R. China.

出版信息

Mol Clin Oncol. 2025 Jul 3;23(3):78. doi: 10.3892/mco.2025.2873. eCollection 2025 Sep.

Abstract

RAS genes play crucial roles in regulating important biological processes such as cell growth, differentiation, and apoptosis in normal cells. When RAS genes undergo mutations or abnormal expression, they can become oncogenic drivers, and the oncogenic mechanism of KRAS mutations which drive cancer progression is highly complex. Colorectal cancer carrying KRAS mutation genes often exhibits poor prognosis. Despite the advent of KRAS G12C inhibitors, monotherapy demonstrates suboptimal clinical efficacy in colorectal cancer, which is attributed to primary resistance and limited coverage of prevalent KRAS mutations (such as G12D and G12V). Notably, combinatorial regimens integrating KRASG12C inhibitors with EGFR monoclonal antibodies (such as cetuximab) have doubled objective response rates, highlighting synergistic therapeutic potential.

摘要

RAS基因在调节正常细胞中的重要生物学过程(如细胞生长、分化和凋亡)中发挥着关键作用。当RAS基因发生突变或异常表达时,它们可能成为致癌驱动因素,而驱动癌症进展的KRAS突变的致癌机制非常复杂。携带KRAS突变基因的结直肠癌通常预后较差。尽管KRAS G12C抑制剂已经出现,但单药治疗在结直肠癌中的临床疗效并不理想,这归因于原发性耐药和对常见KRAS突变(如G12D和G12V)的覆盖有限。值得注意的是,将KRASG12C抑制剂与EGFR单克隆抗体(如西妥昔单抗)联合使用的方案使客观缓解率提高了一倍,突出了协同治疗潜力。

相似文献

1
Targeting KRAS in colorectal cancer (Review).
Mol Clin Oncol. 2025 Jul 3;23(3):78. doi: 10.3892/mco.2025.2873. eCollection 2025 Sep.
2
Epidermal growth factor receptor (EGFR) inhibitors for metastatic colorectal cancer.
Cochrane Database Syst Rev. 2017 Jun 27;6(6):CD007047. doi: 10.1002/14651858.CD007047.pub2.
3
Adagrasib in the treatment of colorectal cancer.
Future Oncol. 2025 Jul 6:1-11. doi: 10.1080/14796694.2025.2524311.
8
SEAMARK: phase II study of first-line encorafenib and cetuximab plus pembrolizumab for MSI-H/dMMR V600E-mutant mCRC.
Future Oncol. 2024 Apr;20(11):653-663. doi: 10.2217/fon-2022-1249. Epub 2023 Oct 10.
9
The RAS-MEK-ERK pathway in low-grade serous ovarian cancer.
Gynecol Oncol. 2025 Jul 17;200:22-32. doi: 10.1016/j.ygyno.2025.06.022.
10
Sotorasib plus Panitumumab in Refractory Colorectal Cancer with Mutated G12C.
N Engl J Med. 2023 Dec 7;389(23):2125-2139. doi: 10.1056/NEJMoa2308795. Epub 2023 Oct 22.

本文引用的文献

1
Divarasib plus cetuximab in KRAS G12C-positive colorectal cancer: a phase 1b trial.
Nat Med. 2024 Jan;30(1):271-278. doi: 10.1038/s41591-023-02696-8. Epub 2023 Dec 5.
2
Targeting KRAS in Colorectal Cancer: A Bench to Bedside Review.
Int J Mol Sci. 2023 Jul 27;24(15):12030. doi: 10.3390/ijms241512030.
3
Differential functions of the KRAS splice variants.
Biochem Soc Trans. 2023 Jun 28;51(3):1191-1199. doi: 10.1042/BST20221347.
4
The Therapeutic Landscape for -Mutated Colorectal Cancers.
Cancers (Basel). 2023 Apr 19;15(8):2375. doi: 10.3390/cancers15082375.
5
Origin and Evolution of RAS Membrane Targeting.
Oncogene. 2023 May;42(21):1741-1750. doi: 10.1038/s41388-023-02672-z. Epub 2023 Apr 8.
7
Targeting mutations in colorectal cancer.
Gastroenterol Rep (Oxf). 2022 Dec 30;11:goac083. doi: 10.1093/gastro/goac083. eCollection 2023.
8
Adagrasib with or without Cetuximab in Colorectal Cancer with Mutated G12C.
N Engl J Med. 2023 Jan 5;388(1):44-54. doi: 10.1056/NEJMoa2212419. Epub 2022 Dec 21.
10
Drugging KRAS: current perspectives and state-of-art review.
J Hematol Oncol. 2022 Oct 25;15(1):152. doi: 10.1186/s13045-022-01375-4.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验