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首页> 外文期刊>Molecular Carcinogenesis >CpG site hypermethylation of E-cadherin and Connexin26 genes in hepatocellular carcinomas induced by a choline-deficient L-Amino Acid-defined diet in rats.
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CpG site hypermethylation of E-cadherin and Connexin26 genes in hepatocellular carcinomas induced by a choline-deficient L-Amino Acid-defined diet in rats.

机译:E-钙粘蛋白和连接蛋白26基因在大鼠胆碱缺乏L-氨基酸饮食诱导的肝细胞癌中的CpG位点甲基化。

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摘要

We investigated DNA methylation patterns of E-cadherin and Connexin26 (Cx26) genes in rat hepatocellular carcinomas (HCCs) induced by a choline-deficient L-Amino Acid-defined (CDAA) diet. Six-wks-old F344 male rats were continuously fed with a CDAA diet for 75 wks, and were then killed. A total of five HCCs were obtained, and genomic DNA was extracted from each HCC for assessment of methylation status in the 5' upstream regions of E-cadherin and Cx26 genes by bisulfite sequencing, comparing to two normal liver tissues. The five HCCs showed highly methylated E-cadherin and Cx26 genes, while these genes in two normal liver tissues were all unmethylated. For analysis of gene expression, real-time quantitative reverse transcription (RT)-polymerase chain reaction (PCR) was performed. Expressions of E-cadherin and Cx26 genes were significantly reduced in the five HCCs (P < 0.0001 and P < 0.001, respectively) compared to normal liver tissues, correlating with their methylation statuses. These results suggested that hypermethylation of E-cadherin and Cx26 genes may be involved in the development of HCCs induced by a CDAA diet in rats.
机译:我们调查了胆碱缺乏L-氨基酸定义(CDAA)饮食诱导大鼠肝细胞癌(HCC)中E-钙粘着蛋白和连接蛋白26(Cx26)基因的DNA甲基化模式。六周龄的F344雄性大鼠连续用CDAA饮食喂养75周,然后处死。与两个正常肝脏组织相比,总共获得了五个肝癌,并从每个肝癌中提取了基因组DNA,以通过亚硫酸氢盐测序评估E-钙粘蛋白和Cx26基因的5'上游区域的甲基化状态。五个HCC显示高度甲基化的E-cadherin和Cx26基因,而两个正常肝组织中的这些基因均未甲基化。为了分析基因表达,进行了实时定量逆转录(RT)-聚合酶链反应(PCR)。与正常肝组织相比,五个肝癌中E-cadherin和Cx26基因的表达显着降低(分别为P <0.0001和P <0.001),与它们的甲基化状态相关。这些结果表明,E-钙粘着蛋白和Cx26基因的超甲基化可能参与了CDAA饮食诱导的大鼠肝癌的发生。

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