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首页> 外文期刊>Japanese Journal of Cancer Research >Hypermethylation of the TSLC1 Gene Promoter in Primary Gastric Cancers and Gastric Cancer Cell Lines.
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Hypermethylation of the TSLC1 Gene Promoter in Primary Gastric Cancers and Gastric Cancer Cell Lines.

机译:TSLC1基因启动子在原发性胃癌和胃癌细胞系中的超甲基化。

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摘要

The TSLC1 (tumor suppressor in lung cancer-1) gene is a novel tumor suppressor gene on chromosomal region 11q23.2, and is frequently inactivated by concordant promoter hypermethylation and loss of heterozygosity (LOH) in non-small cell lung cancer (NSCLC). Because LOH on 11q has also been observed frequently in other human neoplasms including gastric cancer, we investigated the promoter methylation status of TSLC1 in 10 gastric cancer cell lines and 97 primary gastric cancers, as well as the corresponding non-cancerous gastric tissues, by bisulfite-SSCP analysis followed by direct sequencing. Allelic status of the TSLC1 gene was also investigated in these cell lines and primary gastric cancers. The TSLC1 promoter was methylated in two gastric cancer cell lines, KATO-III and ECC10, and in 15 out of 97 (16%) primary gastric cancers. It was not methylated in non-cancerous gastric tissues, suggesting that this hypermethylation is a cancer-specific alteration. KATO-III and ECC10 cells retained two alleles of TSLC1, both of which showed hypermethylation, associated with complete loss of gene expression. Most of the primary gastric cancers with promoter methylation also retained heterozygosity at the TSLC1 locus on 11q23.2. These data indicate that bi-allelic hypermethylation of the TSLC1 promoter and resulting gene silencing occur in a subset of primary gastric cancers.
机译:TSLC1(肺癌1中的肿瘤抑制基因)基因是染色体区域11q23.2上的一种新型肿瘤抑制基因,在非小细胞肺癌(NSCLC)中经常因一致的启动子高甲基化和杂合性丧失(LOH)而失活。 。由于在包括胃癌在内的其他人类肿瘤中也经常观察到11q的LOH,我们通过亚硫酸氢盐研究了10种胃癌细胞系和97种原发性胃癌以及相应的非癌性胃组织中TSLC1的启动子甲基化状态。 -SSCP分析,然后直接测序。在这些细胞系和原发性胃癌中还研究了TSLC1基因的等位基因状态。 TSLC1启动子在两种胃癌细胞系KATO-III和ECC10以及97种原发性胃癌中的15种(16%)中被甲基化。它在非癌性胃组织中没有被甲基化,表明这种高甲基化是癌症特异性的改变。 KATO-III和ECC10细胞保留了TSLC1的两个等位基因,它们都显示出高甲基化,与基因表达的完全丧失有关。大多数具有启动子甲基化的原发性胃癌在11q23.2的TSLC1位点也保留了杂合性。这些数据表明,TSLC1启动子的双等位基因超甲基化和导致的基因沉默发生在原发性胃癌的子集中。

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