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常见疣的全基因组表观遗传分析揭示了异常的启动子甲基化。

Epigenome-wide analysis of common warts reveals aberrant promoter methylation.

机构信息

Department of Applied Biological Sciences, Jordan University of Science and Technology, Irbid 22110, Jordan.

Department of Biotechnology and Genetic Engineering, Jordan University of Science and Technology, Irbid 22110, Jordan.

出版信息

Int J Med Sci. 2020 Jan 14;17(2):191-206. doi: 10.7150/ijms.39261. eCollection 2020.

DOI:10.7150/ijms.39261
PMID:32038103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6990892/
Abstract

Epigenetic alteration of host DNA is a common occurrence in both low- and high-risk human papillomavirus (HPV) infection. Although changes in promoter methylation have been widely studied in HPV-associated cancers, they have not been the subject of much investigation in HPV-induced warts, which are a temporary manifestation of HPV infection. The present study sought to examine the differences in promoter methylation between warts and normal skin. To achieve this, DNA was extracted from 24 paired wart and normal skin samples and inputted into the Infinium MethylationEPIC BeadChip microarray. Differential methylation analysis revealed a clear pattern of hyper- and hypomethylation in warts compared to normal skin, and the most differentially methylated promoters were found within the , , , , , and genes as well as the pseudogene. Moreover, pathway analysis showed that the , , and genes were the most common regulators among the most differentially methylated promoters. Since the tissue samples were excised from active warts, however, this differential methylation could either be a cellular response to HPV infection or an HPV-driven process to establish the wart and/or promote disease progression. Conclusively, it is apparent that HPV infection alters the methylation status of certain genes to possibly initiate the formation of a wart and maintain its presence.

摘要

宿主 DNA 的表观遗传改变在低危和高危人乳头瘤病毒 (HPV) 感染中都很常见。尽管 HPV 相关癌症中广泛研究了启动子甲基化的变化,但在 HPV 引起的疣中,这些变化并没有得到太多研究,疣是 HPV 感染的暂时表现。本研究旨在研究疣和正常皮肤之间启动子甲基化的差异。为此,从 24 对疣和正常皮肤样本中提取 DNA,并输入 Infinium MethylationEPIC BeadChip 微阵列。差异甲基化分析显示,与正常皮肤相比,疣中存在明显的高甲基化和低甲基化模式,最具差异甲基化的启动子位于 、 、 、 、 和 基因以及 假基因内。此外,通路分析表明,最具差异甲基化的启动子中最常见的调节因子是 、 和 基因。然而,由于组织样本是从活跃的疣中切除的,因此这种差异甲基化可能是 HPV 感染对细胞的反应,也可能是 HPV 驱动的过程,以建立疣并促进疾病进展。总之,很明显,HPV 感染改变了某些基因的甲基化状态,可能导致疣的形成并维持其存在。

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