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Genome-wide analysis of DNA methylation profile identifies differentially methylated loci associated with human intervertebral disc degeneration

机译:全基因组分析的DNA甲基化谱可识别与人椎间盘退变相关的甲基化位点

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摘要

BackgroundEnvironmental and endogenous factors under genetic predisposition are considered to initiate the human intervertebral disc (IVD) degeneration. DNA methylation is an essential mechanism to ensure cell-specific gene expression for normal development and tissue stability. Aberrant epigenetic alterations play a pivotal role in several diseases, including osteoarthritis. However, epigenetic alternations, including DNA methylation, in IVD degeneration have not been evaluated. The purpose of this study was to comprehensively compare the genome-wide DNA methylation profiles of human IVD tissues, specifically nucleus pulpous (NP) tissues, with early and advanced stages of disc degeneration.
机译:背景技术考虑遗传易感性的环境和内源性因素引发人类椎间盘(IVD)变性。 DNA甲基化是确保正常发育和组织稳定的细胞特异性基因表达的重要机制。异常的表观遗传改变在包括骨关节炎在内的几种疾病中起着关键作用。但是,尚未评估IVD变性中的表观遗传改变,包括DNA甲基化。这项研究的目的是全面比较人类IVD组织(特别是髓核(NP)组织)与椎间盘退变的早期和晚期阶段的全基因组DNA甲基化分布。

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