首页> 外文期刊>European Journal of Surgical Oncology: The Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology >Germline mutational analysis of CDH1 and pathologic features in familial cancer syndrome with diffuse gastric cancer/breast cancer proband in a Chinese family.
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Germline mutational analysis of CDH1 and pathologic features in familial cancer syndrome with diffuse gastric cancer/breast cancer proband in a Chinese family.

机译:中国家庭弥漫性胃癌/乳腺癌先证者的家族性癌症综合征CDH1的种系突变分析和病理特征。

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Aims. Hereditary non-polyposis colorectal cancer, thyroid medullary carcinoma, breast/ovarian cancer and gastric cancer/breast cancer syndrome are encountered in surgery. Some gastric cancer/breast cancer syndrome may be the result of a CDH1 germline mutation. This is the first report of CDH1 germline mutations gastric cancer/breast cancer syndrome in Chinese patients. Methods. Peripheral blood from the proband, as well as, her first and second degree relatives was collected and CDH1 gene exon 1-16 mutations were screened. E-cadherin/beta-catenin proteins expression and histopathologic features were examined on gastric cancer/breast cancer tissues from the proband. Results. A C-->T nucleotide substitution at exon 13 (mRNA 2200 locus, Accession number NM-004360) was found. This was a transition from GCC-->GCT in DNA sequence (Ala154Ala). Diffuse-type gastric cancer and infiltrating ductal breast carcinoma were present. Both tumours preserved E-cadherin/beta-catenin expression immunohistochemically. Conclusions. Familial cancer syndrome with diffuse-type gastric cancer/breast cancer proband in Chinese has a propensity of early onset during lifespan. No truncating or splice-site CDH1 mutations had been identified in this family. A silent nucleotide variation in exon 13 of the CDH1 gene may contribute to some forms of cancer susceptibility.
机译:目的遗传性非息肉性大肠癌,甲状腺髓样癌,乳腺癌/卵巢癌和胃癌/乳腺癌综合征在手术中会遇到。一些胃癌/乳腺癌综合征可能是CDH1种系突变的结果。这是中国患者CDH1种系突变胃癌/乳腺癌综合征的首次报道。方法。先证者及其一级和二级亲戚的外周血均被收集,并筛选了CDH1基因外显子1-16突变。在先证者的胃癌/乳腺癌组织上检查了E-钙黏着蛋白/β-连环蛋白的表达和组织病理学特征。结果。发现在第13外显子(mRNA 2200基因座,登录号NM-004360)处有C→T核苷酸取代。这是DNA序列(Ala154Ala)从GCC→GCT的过渡。存在弥漫型胃癌和浸润性导管癌。两种肿瘤均通过免疫组织化学方法保留了E-钙粘蛋白/β-连环蛋白的表达。结论中国人具有弥漫型胃癌/乳腺癌先兆的家族性癌症综合症在寿命中倾向于早发。该家族中没有发现截短或剪接位点的CDH1突变。 CDH1基因第13外显子的沉默核苷酸变异可能有助于某种形式的癌症易感性。

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