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胃癌易感性基因的疾病谱。

Disease spectrum of gastric cancer susceptibility genes.

机构信息

Department of Surgery, Massachusetts General Hospital, Boston, MA, USA.

Division of Surgical Oncology, Massachusetts General Hospital and Harvard Medical School, 55 Fruit Street, Yawkey 7, Boston, MA, 02114, USA.

出版信息

Med Oncol. 2021 Mar 24;38(5):46. doi: 10.1007/s12032-021-01495-w.

Abstract

Pathogenic variants in germline cancer susceptibility genes can increase the risk of a large number of diseases. Our study aims to assess the disease spectrum of gastric cancer susceptibility genes and to develop a comprehensive resource of gene-disease associations for clinicians. Twenty-seven potential germline gastric cancer susceptibility genes were identified from three review articles and from six commonly used genetic information resources. The diseases associated with each gene were evaluated via a semi-structured review of six genetic resources and an additional literature review using a natural language processing (NLP)-based procedure. Out of 27 candidate genes, 13 were identified as gastric cancer susceptibility genes (APC, ATM, BMPR1A, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH-Biallelic, PALB2, SMAD4, and STK11). A total of 145 gene-disease associations (with 45 unique diseases) were found to be associated with these 13 genes. Other gastrointestinal cancers were prominent among identified associations, with 11 of 13 gastric cancer susceptibility genes also associated with colorectal cancer, eight genes associated with pancreatic cancer, and seven genes associated with small intestine cancer. Gastric cancer susceptibility genes are frequently associated with other diseases as well as gastric cancer, with potential implications for how carriers of these genes are screened and managed. Unfortunately, commonly used genetic resources provide heterogeneous information with regard to these genes and their associated diseases, highlighting the importance of developing guides for clinicians that integrate data across available resources and the medical literature.

摘要

种系癌症易感性基因中的致病变异可增加多种疾病的风险。我们的研究旨在评估胃癌易感性基因的疾病谱,并为临床医生开发一个全面的基因-疾病关联资源。从三篇综述文章和六个常用的遗传信息资源中确定了 27 个潜在的种系胃癌易感性基因。通过对六个遗传资源进行半结构化审查以及使用基于自然语言处理 (NLP) 的程序进行额外的文献综述,评估了与每个基因相关的疾病。在 27 个候选基因中,确定了 13 个胃癌易感性基因 (APC、ATM、BMPR1A、CDH1、CHEK2、EPCAM、MLH1、MSH2、MSH6、MUTYH-Biallelic、PALB2、SMAD4 和 STK11)。发现这些基因与 145 种基因-疾病关联(45 种独特疾病)有关。确定的关联中以其他胃肠道癌为主,13 个胃癌易感性基因中有 11 个与结直肠癌相关,8 个与胰腺癌相关,7 个与小肠癌相关。胃癌易感性基因也经常与其他疾病以及胃癌相关,这对这些基因携带者的筛查和管理方式有潜在影响。不幸的是,常用的遗传资源在这些基因及其相关疾病方面提供了异构信息,这突出了为临床医生开发整合可用资源和医学文献中数据的指南的重要性。

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