中国错配修复基因(MMR)种系突变携带者群体筛查综述

IF 2 4区 医学 Q3 ONCOLOGY Hereditary Cancer in Clinical Practice Pub Date : 2021-05-01 DOI:10.1186/s13053-021-00182-1
Min Zhang, Tianhui Chen
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引用次数: 4

摘要

DNA错配修复(DNA mismatch repair, MMR)基因在维持基因组稳定性中起着重要作用。MMR基因的种系突变破坏错配修复功能并导致基因组不稳定。与非携带者相比,携带MMR种系突变的携带者更容易出现MMR缺陷和微卫星不稳定性(MSI),并且更容易发生结直肠癌(CRC)和结直肠外恶性肿瘤,即Lynch综合征(LS)。对疑似突变携带者进行MMR基因检测是鉴定突变类型和发现突变携带者的可靠方法。鉴于MMR种系突变携带者发生ls相关癌症(LS-RC)的风险高于非携带者,且发病年龄更小,因此对携带者的相关器官进行早期监测和定期筛查对于早期发现相关癌症非常重要。本文主要综述了中国MMR突变携带者的概况、早期发现和筛查方法以及MMR突变携带者的监测情况。对中国MMR种系突变携带者进行人群筛查,有助于MMR突变携带者的早期发现、早期诊断和早期治疗,提高5年生存率,长期降低死亡率和发病率。
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Overview on population screening for carriers with germline mutations in mismatch repair (MMR) genes in China.

DNA mismatch repair (MMR) genes play an important role in maintaining genome stability. Germline mutations in MMR genes disrupt the mismatch repair function and cause genome instability. Carriers with MMR germline mutations are more likely to have MMR deficiency and microsatellite instability (MSI) than non-carriers and are prone to develop colorectal cancer (CRC) and extracolorectal malignancies, known as Lynch syndrome (LS). MMR gene testing for suspected mutation carriers is a reliable method to identify the mutation types and to discover mutation carriers. Given that carriers of MMR germline mutations have a higher risk of LS-related cancers (LS-RC) and a younger age at onset than non-carriers, early surveillance and regular screening of relevant organs of carriers are very important for early detection of related cancers. This review mainly focuses on the general status of MMR carriers, the approaches for early detection and screening, and the surveillance of MMR mutation carriers in China. Population screening of MMR germline mutation carriers in China will be helpful for early detection, early diagnosis and treatment of MMR mutation carriers, which may improve the 5-year survival, and reduce mortality and incidence rate in the long term.

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来源期刊
CiteScore
3.10
自引率
5.90%
发文量
38
审稿时长
>12 weeks
期刊介绍: Hereditary Cancer in Clinical Practice is an open access journal that publishes articles of interest for the cancer genetics community and serves as a discussion forum for the development appropriate healthcare strategies. Cancer genetics encompasses a wide variety of disciplines and knowledge in the field is rapidly growing, especially as the amount of information linking genetic differences to inherited cancer predispositions continues expanding. With the increased knowledge of genetic variability and how this relates to cancer risk there is a growing demand not only to disseminate this information into clinical practice but also to enable competent debate concerning how such information is managed and what it implies for patient care. Topics covered by the journal include but are not limited to: Original research articles on any aspect of inherited predispositions to cancer. Reviews of inherited cancer predispositions. Application of molecular and cytogenetic analysis to clinical decision making. Clinical aspects of the management of hereditary cancers. Genetic counselling issues associated with cancer genetics. The role of registries in improving health care of patients with an inherited predisposition to cancer.
期刊最新文献
BRCA2 germline mutation carrier with five malignancies: a case report. A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives. Breast cancer and ATM mutations: treatment implications. Meeting abstracts from the Annual Conference "Clinical Genetics of Cancer 2023". Validation of a guidelines-based digital tool to assess the need for germline cancer genetic testing.
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