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Analyses of methylation status of CpG islands in promoters of miR-9 genes family in human gastric adenocarcinoma

机译:人胃腺癌miR-9基因家族启动子中CpG岛甲基化状态的分析

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摘要

In the recent years deregulation for microRNAs expression pattern have emerged as a possible molecular factor for carcinogenesis. It has been reported that the expression of miR-9 was down-regulated in human gastric adenocarcinoma. To figure out the molecular mechanism of this down regulation, the methylation status in promoters of miR-9 family loci were compared in the human gastric adenocarcinoma samples with their normal margins. Using a methylation specific PCR technique the methylation status of miR-9 family loci were compared between 30 pairs of primary human gastric adenocarcinoma samples with their normal margins. The methylation of miR 9-1 status showed no specific difference in promoter methylation pattern in tumor and normal specimens, while in the miR-9-2 locus were unmethylated in both types of tissues. The promoter of miR-9-3 locus seems to be specifically methylated in tumor and their normal margin tissues. Our data revealed methylation of these CpG islands were not meaningfully different between normal and tumor gastric adenocarcinoma specimens and the methylation status of promoter may not be able to account for alteration of miR-9 expression in this type of gastric cancer.
机译:近年来,对microRNA表达模式的放松调控已成为可能的致癌分子因素。据报道,miR-9的表达在人胃腺癌中被下调。为了弄清楚这种下调的分子机制,在人胃腺癌样品中以正常边缘比较了miR-9家族基因启动子的甲基化状态。使用甲基化特异性PCR技术,在30对原发性人胃腺癌样本中,以正常边缘比较了miR-9家族基因座的甲基化状态。在肿瘤和正常标本中,miR 9-1状态的甲基化未显示启动子甲基化模式的特异性差异,而在两种类型的组织中,miR-9-2位点均未甲基化。 miR-9-3基因座的启动子似乎在肿瘤及其正常边缘组织中被特异性甲基化。我们的数据显示这些CpG岛的甲基化在正常和肿瘤胃腺癌标本之间没有显着差异,并且启动子的甲基化状态可能无法解释这种类型的胃癌中miR-9表达的改变。

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