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Germline mutations in hereditary diffuse gastric cancer

机译:遗传性弥漫性胃癌的生殖系突变

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摘要

Gastric cancer is one of the leading causes of cancer-related deaths worldwide.Among which,about 1%-3% of gastric cancer patients were characterized by inherited gastric cancer predisposition syndromes,knowing as hereditary diffuse gastric cancer (HDGC).Studies reported that CDH1 germline mutations are the main cause of HDGC.With the help of rapid development of genetic testing technologies and data analysis tools,more and more researchers focus on seeking candidate susceptibility genes for hereditary cancer syndromes.In addition,National Comprehensive Cancer Network (NCCN) guidelines recommend that the patients of HDGC carrying CDH1 mutations should undergo prophylactic gastrectomy or routine endoscopic surveillances.Therefore,genetic counseling plays a key role in helping individuals with pathogenic mutations make appropriate risk management plans.Moreover,experienced and professional genetic counselors as well as a systematic multidisciplinary team (MDT) are also required to facilitate the development of genetic counseling and benefit pathogenic mutation carriers who are in need of regular and standardized risk management solutions.In this review,we provided an overview about the germline mutations of several genes identified in HDGC,suggesting that these genes may potentially act as susceptibility genes for this malignant cancer syndrome.Furthermore,we introduced information for prevention,diagnosis and risk management of HDGC.Investigations on key factors that may have effect on risk management decision-making and genetic data collection of more cancer syndrome family pedigrees are required for the development of HDGC therapeutic strategies.
机译:胃癌是全球范围内与癌症相关的死亡的主要原因之一。其中,约有1%-3%的胃癌患者具有遗传性胃癌易感综合征,被称为遗传性弥漫性胃癌(HDGC)。研究报道: CDH1种系突变是HDGC的主要原因。借助于基因检测技术和数据分析工具的迅速发展,越来越多的研究人员致力于寻找遗传性癌症综合征的候选易感基因。此外,国家综合癌症网络(NCCN)指南建议携带CDH1突变的HDGC患者应进行预防性胃切除术或常规内窥镜检查。因此,遗传咨询在帮助具有致病性突变的个体制定适当的风险管理计划中起着关键作用。此外,经验丰富且专业的遗传咨询师以及还需要系统的多学科团队(MDT)来促进进行遗传咨询,使需要常规和标准化风险管理解决方案的致病突变携带者受益。在这篇综述中,我们概述了HDGC中鉴定的几种基因的种系突变,表明这些基因可能具有潜在的作用。此外,我们还介绍了HDGC的预防,诊断和风险管理信息。需要对可能影响更多癌症综合征家族谱系的风险管理决策和遗传数据收集的关键因素进行调查。 HDGC治疗策略的发展。

著录项

  • 来源
    《中国癌症研究(英文版)》 |2018年第1期|122-130|共9页
  • 作者单位

    Surgery Laboratory, the Affiliated Hospital of Inner Mongolia Medical University, Hohhot 010050, China;

    Key Laboratory of Carcinogenesis and Translational Research(Ministry of Education/Beijing), Department of Molecular Diagnostics, Peking University Cancer Hospital & Institute,Beijing 100142, China;

    Department of Gynecology, Weifang Maternal and Child Health Hospital, Weifang 261011, China;

    Key Laboratory of Carcinogenesis and Translational Research(Ministry of Education/Beijing), Department of Molecular Diagnostics, Peking University Cancer Hospital & Institute,Beijing 100142, China;

    Key Laboratory of Carcinogenesis and Translational Research(Ministry of Education/Beijing), Center of Gastrointestinal Surgery, Peking University Cancer Hospital &Institute, Beijing 100142, China;

    Key Laboratory of Carcinogenesis and Translational Research(Ministry of Education/Beijing), Center of Gastrointestinal Surgery, Peking University Cancer Hospital &Institute, Beijing 100142, China;

    Surgery Laboratory, the Affiliated Hospital of Inner Mongolia Medical University, Hohhot 010050, China;

    Key Laboratory of Carcinogenesis and Translational Research(Ministry of Education/Beijing), Department of Molecular Diagnostics, Peking University Cancer Hospital & Institute,Beijing 100142, China;

    Key Laboratory of Carcinogenesis and Translational Research(Ministry of Education/Beijing), Center of Gastrointestinal Surgery, Peking University Cancer Hospital &Institute, Beijing 100142, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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