Department of Cancer Biology and Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.
Department of Cancer Biology and Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA; Department of Internal Medicine, Division of Human Genetics, The Ohio State University, Columbus, OH, USA.
Trends Cancer. 2024 May;10(5):444-456. doi: 10.1016/j.trecan.2024.01.008. Epub 2024 Feb 14.
Immunotherapy shows efficacy for multiple cancer types and potential for expanded use. However, current immune checkpoint inhibitors (ICIs) are ineffective against microsatellite-stable colorectal cancer (CRC), which is more commonly diagnosed. Immunotherapy strategies for non-responsive CRC, including new targets and new combination therapies, are being tested to address this need. Importantly, a subset of inherited germline genetic variants associated with CRC risk are predicted to regulate genes with immune functions, including genes related to existing ICIs, as well as new potential targets in the major histocompatibility complex (MHC) region and immunoregulatory cytokines. We review discoveries in the inherited genetics of CRC related to the immune system and draw connections with ongoing developments and emerging immunotherapy targets.
免疫疗法在多种癌症类型中显示出疗效,并具有扩大应用的潜力。然而,目前的免疫检查点抑制剂(ICIs)对微卫星稳定的结直肠癌(CRC)无效,而 CRC 的诊断更为常见。正在测试针对非应答性 CRC 的免疫治疗策略,包括新的靶点和新的联合疗法,以满足这一需求。重要的是,与 CRC 风险相关的一组遗传性种系遗传变异被预测可调节具有免疫功能的基因,包括与现有 ICIs 相关的基因,以及主要组织相容性复合体(MHC)区域和免疫调节细胞因子中的新潜在靶点。我们回顾了结直肠癌与免疫系统相关的遗传发现,并将其与正在进行的发展和新兴免疫治疗靶点联系起来。