Zhang Minjie, Wu Dawei, Tang Yu, Zhang Li, Zhang Shuquan, Li Wei, Li Ning, Yan Xinhua
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.
Mol Clin Oncol. 2025 Jul 3;23(3):78. doi: 10.3892/mco.2025.2873. eCollection 2025 Sep.
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.
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。