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首页> 外文期刊>Familial cancer >Prophylactic total gastrectomy in hereditary diffuse gastric cancer: Identification of two novel CDH1 gene mutations - A clinical observational study
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Prophylactic total gastrectomy in hereditary diffuse gastric cancer: Identification of two novel CDH1 gene mutations - A clinical observational study

机译:遗传性弥漫性胃癌的预防性全胃切除术:鉴定两个新的CDH1基因突变-临床观察性研究

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Inactivating mutations in the CDH1 (E-cadherin) gene are the predisposing cause of gastric cancer in most families with hereditary diffuse gastric cancer (HDGC). The lifetime risk of cancer in mutation positive members is more than 80 % and prophylactic total gastrectomy is recommended. Not all mutations in the CDH1 gene are however pathogenic and it is important to classify mutations before this major operation is performed. Probands from two Danish families with gastric cancer and a history suggesting HDGC were screened for CDH1 gene mutations. Two novel CDH1 gene mutations were identified and found pathogenic. In silico and mini-gene assay were used to predict the functional consequence in one of them. Mutation carriers were offered endoscopy and total gastrectomy. The gastric specimens were completely sectioned and examined histologically. Seven asymptomatic mutation carriers were operated. Hospital stay was 6-8 days and there were no complications. Small foci of diffuse gastric cancer were found in all patients-intramucosal in six and advanced in one. Preoperative endoscopic biopsies had revealed a microscopic cancer focus in two of the patients. Our data confirmed the pathogenic nature of both mutations and strongly support the recommendation of total gastrectomy in asymptomatic CDH1 gene mutation carriers. The functional consequences of novel CDH1 gene mutations with uncertain effects should be tested before correct advice and treatment can be given.
机译:CDH1(E-钙粘着蛋白)基因的失活突变是遗传性弥漫性胃癌(HDGC)的大多数家庭中胃癌的诱因。突变阳性成员的终生癌症风险超过80%,因此建议进行预防性全胃切除术。但是,并非CDH1基因中的所有突变都具有致病性,因此在执行此主要操作之前对突变进行分类非常重要。对来自丹麦两个患有胃癌的家庭的先证者以及有史以来暗示HDGC的患者进行了CDH1基因突变筛查。鉴定出两个新的CDH1基因突变并发现其致病性。在计算机和微型基因分析中,预测其中之一的功能后果。突变载体提供了内窥镜和全胃切除术。将胃标本完全切开并进行组织学检查。七个无症状突变携带者进行了手术。住院时间为6-8天,没有并发症。在所有患者中均发现了弥漫性胃癌的小灶,其中有6例粘膜内粘膜癌,有1例进展。术前内窥镜活检显示两名患者有微小的癌灶。我们的数据证实了这两种突变的致病性,并强烈支持在无症状CDH1基因突变携带者中进行全胃切除的建议。在给予正确建议和治疗之前,应测试具有不确定效果的新型CDH1基因突变的功能后果。

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