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Microsatellite instability analysis in hereditary non-polyposis colon cancer using the Bethesda consensus panel of microsatellite markers in the absence of proband normal tissue

机译:在没有先证者正常组织的情况下使用贝塞斯达(Bethesda)共识性微卫星标记物组对遗传性非息肉性结肠癌的微卫星不稳定性分析

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摘要

BackgroundHereditary non-polyposis colon cancer (HNPCC) is an autosomal dominant syndrome predisposing to the early development of various cancers including those of colon, rectum, endometrium, ovarium, small bowel, stomach and urinary tract. HNPCC is caused by germline mutations in the DNA mismatch repair genes, mostly hMSH2 or hMLH1.In this study, we report the analysis for genetic counseling of three first-degree relatives (the mother and two sisters) of a male who died of colorectal adenocarcinoma at the age of 23. The family fulfilled strict Amsterdam-I criteria (AC-I) with the presence of extracolonic tumors in the extended pedigree. We overcame the difficulty of having a proband post-mortem non-tumor tissue sample for MSI testing by studying the alleles carried by his progenitors.
机译:背景遗传性非息肉性结肠癌(HNPCC)是常染色体显性综合征,易患各种癌症,包括结肠癌,直肠癌,子宫内膜癌,卵巢癌,小肠癌,胃癌和泌尿道癌。 HNPCC是由DNA错配修复基因中的种系突变引起的,主要是hMSH2或hMLH1。在这项研究中,我们报告了对死于结肠直肠腺癌的男性的三个一级亲属(母亲和两个姐妹)进行遗传咨询的分析。在23岁时,这个家庭符合严格的Amsterdam-I标准(AC-I),而家系中存在结肠外肿瘤。我们通过研究其祖先携带的等位基因,克服了先证者死后非肿瘤组织样品用于MSI测试的难题。

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