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Array-based profiling of the differential methylation status of CpG islands in hepatocellular carcinoma cell lines

机译:基于阵列的肝癌细胞株中CpG岛甲基化状态差异分析

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摘要

Alterations in the DNA methylation status particularly in CpG islands are involved in the initiation and progression of many types of human cancer. A number of DNA methylation alterations have been reported in hepatocellular carcinoma (HCC). However, a systematic analysis is required to elucidate the relationship between differential DNA methylation status and the characteristics and progression of HCC. In the present study, a global analysis of DNA methylation using a human CpG-island 12K array was performed on a number of HCC cell lines of different origin and metastatic potential. Based on a standard methylation alteration ratio of ≥2 or ≤0.5, 58 CpG island sites and 66 tumor-related genes upstream, downstream or within were identified. This study showed a series of CpG island methylation alterations in the HCC cell lines. The expression of various oncogenes, tumor suppressor genes and other key genes were up- or downregulated, respectively, resulting in CpG island hypomethylation or hypermethylation accordingly. To conclude, a foundation has been provided for screening CpG island methylation profiles as HCC biological markers.
机译:DNA甲基化状态的改变,特别是在CpG岛中,涉及许多类型的人类癌症的发生和发展。肝细胞癌(HCC)中已报道了许多DNA甲基化改变。但是,需要系统分析来阐明差异DNA甲基化状态与HCC特征和进展之间的关系。在本研究中,对许多具有不同起源和转移潜力的HCC细胞系进行了使用人类CpG-island 12K阵列的DNA甲基化的全局分析。基于≥2或≤0.5的标准甲基化改变率,鉴定了58个CpG岛位点和66个与肿瘤相关的基因的上游,下游或内部。这项研究显示了HCC细胞系中一系列CpG岛甲基化改变。各种癌基因,肿瘤抑制基因和其他关键基因的表达分别被上调或下调,从而导致CpG岛低甲基化或高甲基化。总之,为筛选CpG岛甲基化谱作为HCC生物标志物提供了基础。

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