摘要:肿瘤是可预测的吗?遗传免疫变异限制肿瘤进化

Rachel Marty, S. Kaabinejadian, David Rossel, M. Slifker, J. L. D. Haar, H. Engin, N. Prisco, T. Ideker, W. Hildebrand, Joan Font-Burgada, H. Carter
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引用次数: 0

摘要

最近的研究已经描述了癌症期间出现的广泛的体细胞改变,各种研究已经探索了导致早发性癌症综合征的罕见遗传突变。然而,人们对遗传背景在“散发性”成年癌症中的作用知之甚少。肿瘤的体细胞进化可能受到生殖系中携带的遗传多态性的显著影响。编码主要组织相容性复合体I类(MHC-I)的区域是人类中最可变的区域之一。mhc - 1是一种暴露细胞表面细胞内蛋白质含量的分子,允许T细胞检测突变或外源肽。每个人都携带6个mhc - 1等位基因,这些等位基因定义了一组可以有效地用于免疫监视的肽。我们假设MHC-I的个体差异可能会在免疫监视中造成个人空白,从而产生个体对细胞获得特定致癌突变的特异性易感性。我们通过对9176名癌症患者中1018例复发性致癌突变的残留物为中心的患者表现评分的开发和应用来检验这一假设。该分析发现,当患者基于基因型的评分表明这些突变基于MHC-I的表现较差时,更有可能观察到致癌突变。在大多数患者中表现不佳的突变也更有可能在肿瘤中达到高频率。因此,在临床诊断的肿瘤中观察到的致癌突变景观是由肿瘤形成过程中MHC-I基因型限制性免疫编辑塑造的,而个体MHC-I基因型提供了在生命后期发展的肿瘤中可能出现的突变的信息。引文格式:Rachel Marty, Saghar Kaabinejadian, David Rossel, Michael J. Slifker, Joris Van de Haar, Hattice Billur Engin, Nicola de Prisco, Trey Ideker, William H. Hildebrand, Joan Font-Burgada, Hannah Carter。肿瘤是可预测的吗?遗传免疫变异制约肿瘤进化[摘要]。第五届AACR-IASLC国际联合会议论文集:肺癌转化科学从实验室到临床;2018年1月8日至11日;费城(PA): AACR;临床肿瘤杂志,2018;24(17 -增刊):摘要1 - 24。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract IA24: Are tumors predictable? Inherited immune variation constrains tumor evolution
Recent studies have characterized the extensive somatic alterations that arise during cancer, and various studies have probed rare inherited mutations that lead to early-onset cancer syndromes. However, little is understood about the role of genetic background in “sporadic” adulthood cancers. The somatic evolution of a tumor may be significantly affected by inherited polymorphisms carried in the germline. The region encoding the Major Histocompatibility Complex Class I (MHC-I) is one of the most variable regions in the human population. MHC-I is a molecule that exposes the intracellular protein content of a cell on the cell surface, allowing T cells to detect mutated or foreign peptides. Each individual carries six MHC-I alleles that define the set of peptides that can be effectively presented for immune surveillance. We hypothesized that individual variation in MHC-I could create personal gaps in immune surveillance, generating individual-specific susceptibility for cells to acquire specific oncogenic mutations. We tested this hypothesis through the development and application of a residue-centric patient presentation score to 1,018 recurrent oncogenic mutations in 9,176 cancer patients. This analysis found that cancer-causing mutations were more likely to be observed when a patient’s genotype-based scores suggested poor MHC-I based presentation of those mutations. Mutations that were poorly presented by most patients were also more likely to reach high frequency among tumors. Thus the landscape of oncogenic mutations observed in clinically diagnosed tumors is shaped by MHC-I genotype-restricted immunoediting during tumor formation, and individual MHC-I genotype provides information about the mutations likely to emerge in tumors that develop later in life. Citation Format: Rachel Marty, Saghar Kaabinejadian, David Rossel, Michael J. Slifker, Joris Van de Haar, Hattice Billur Engin, Nicola de Prisco, Trey Ideker, William H. Hildebrand, Joan Font-Burgada, Hannah Carter. Are tumors predictable? Inherited immune variation constrains tumor evolution [abstract]. In: Proceedings of the Fifth AACR-IASLC International Joint Conference: Lung Cancer Translational Science from the Bench to the Clinic; Jan 8-11, 2018; San Diego, CA. Philadelphia (PA): AACR; Clin Cancer Res 2018;24(17_Suppl):Abstract nr IA24.
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