Ding Xinyi, Huang Hao, Fang Zhang, Jiang Jingting
Department of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, 213003, Jiangsu Province, China.
Jiangsu Engineering Research Center for Tumor Immunotherapy, The Third Affiliated Hospital of Soochow University, Changzhou, 213003, Jiangsu, China.
Curr Treat Options Oncol. 2024 Dec;25(12):1580-1593. doi: 10.1007/s11864-024-01282-5. Epub 2024 Nov 26.
The biological heterogeneity of colorectal cancer makes its molecular characteristics essential for therapeutic decision-making and prognostic evaluation. Recent advancements in consensus molecular subtyping, based on gene expression profiling, have provided deeper insights into the heterogeneity of CRC. CMS1, known as the immune subtype, is characterized by robust immune activity and microsatellite instability. CMS2, the canonical subtype, exhibits significant activation of the WNT and MYC signaling pathways. CMS3, the metabolic subtype, features unique metabolic dysregulations. CMS4, the mesenchymal subtype, is recognized for its stromal invasion and angiogenesis, which are associated with a poorer prognosis. This review delivers a thorough analysis of the biological and clinical responses of each CMS subtype in colorectal cancer, highlighting their therapeutic vulnerabilities. It integrates data and clinical trial results to suggest potential new therapies for each subtype. The goal is to improve therapeutic efficacy, minimize treatment disparities, and offer CRC patients more precise treatment options.
结直肠癌的生物学异质性使其分子特征对于治疗决策和预后评估至关重要。基于基因表达谱的共识分子亚型分类法的最新进展,为深入了解结直肠癌的异质性提供了更多见解。CMS1,即免疫亚型,其特征是强大的免疫活性和微卫星不稳定性。CMS2,即经典亚型,表现出WNT和MYC信号通路的显著激活。CMS3,即代谢亚型,具有独特的代谢失调特征。CMS4,即间充质亚型,因其基质侵袭和血管生成而被识别,这与较差的预后相关。本综述对结直肠癌中各CMS亚型的生物学和临床反应进行了全面分析,突出了它们在治疗上的脆弱性。它整合了数据和临床试验结果,为每个亚型提出了潜在的新疗法。目标是提高治疗效果,尽量减少治疗差异,并为结直肠癌患者提供更精确的治疗选择。