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晚期结直肠癌中的免疫亚型与新抗原相关的免疫逃逸

Immune subtypes and neoantigen-related immune evasion in advanced colorectal cancer.

作者信息

Sugawara Toshitaka, Miya Fuyuki, Ishikawa Toshiaki, Lysenko Artem, Nishino Jo, Kamatani Takashi, Takemoto Akira, Boroevich Keith A, Kakimi Kazuhiro, Kinugasa Yusuke, Tanabe Minoru, Tsunoda Tatsuhiko

机构信息

Department of Hepatobiliary and Pancreatic Surgery, Graduate School of Medicine, Tokyo Medical and Dental University (TMDU), Tokyo 113-8510, Japan.

Department of Medical Science Mathematics, Medical Research Institute, Tokyo Medical and Dental University (TMDU), Tokyo 113-8510, Japan.

出版信息

iScience. 2022 Jan 6;25(2):103740. doi: 10.1016/j.isci.2022.103740. eCollection 2022 Feb 18.

Abstract

Elimination of cancerous cells by the immune system is an important mechanism of protection from cancer, however, its effectiveness can be reduced owing to development of resistance and evasion. To understand the systemic immune response in advanced untreated primary colorectal cancer, we analyze immune subtypes and immune evasion via neoantigen-related mechanisms. We identify a distinctive cancer subtype characterized by immune evasion and very poor overall survival. This subtype has less clonal highly expressed neoantigens and high chromosomal instability, resulting in adaptive immune resistance mediated by the immune checkpoint molecules and neoantigen presentation disorders. We also observe that neoantigen depletion caused by immunoediting and high clonal neoantigen load are correlated with a good overall survival. Our results indicate that the status of the tumor microenvironment and neoantigen composition are promising new prognostic biomarkers with potential relevance for treatment plan decisions in advanced CRC.

摘要

免疫系统清除癌细胞是预防癌症的重要保护机制,然而,由于耐药性和免疫逃逸的发展,其有效性可能会降低。为了解晚期未经治疗的原发性结直肠癌中的全身免疫反应,我们通过新抗原相关机制分析免疫亚型和免疫逃逸。我们鉴定出一种以免疫逃逸和总体生存率极低为特征的独特癌症亚型。该亚型具有较少的克隆性高表达新抗原和高染色体不稳定性,导致由免疫检查点分子介导的适应性免疫抵抗和新抗原呈递障碍。我们还观察到免疫编辑导致的新抗原耗竭和高克隆新抗原负荷与良好的总体生存率相关。我们的结果表明,肿瘤微环境状态和新抗原组成是有前景的新预后生物标志物,可能与晚期结直肠癌的治疗方案决策相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33ef/8800070/dff7a4881555/fx1.jpg

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