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miRNA-375 在 2 型糖尿病患者中的表达及 DNA 甲基化状态。

Expression and DNA methylation status of microRNA-375 in patients with type 2 diabetes mellitus.

机构信息

Department of Endocrinology and Metabolism, First Affiliated Hospital, Shihezi University School of Medicine, Shihezi, Xinjiang 832002, P.R. China.

The Central Laboratory, First Affiliated Hospital, Shihezi University School of Medicine, Shihezi, Xinjiang 832002, P.R. China.

出版信息

Mol Med Rep. 2014 Mar;9(3):967-72. doi: 10.3892/mmr.2013.1872. Epub 2013 Dec 18.

Abstract

Recent studies have shown that DNA methylation in the promoter of microRNA-375 (miR-375) downregulates its expression during tumorigenesis. However, it is not known if CpG methylation of the miR-375 promoter also has a role in the pathogenesis of type 2 diabetes mellitus (T2DM). In this study, the expression level and CpG methylation status of miR-375 in patients with T2DM were analyzed. Plasma samples from 100 patients with T2DM and 100 healthy controls with normal glucose tolerance (NGT) were collected. The plasma levels of miR-375 were examined using quantitative polymerase chain reaction (qPCR) and the methylation status of 17 CpG sites in the promoter of the miR-375 were determined using MassARRAY spectrometry. The plasma levels of miR-375 were found to be upregulated in patients with T2DM compared with controls with NGT (P<0.05). Overall, the methylation levels of the miR-375 promoter in patients with T2DM were not significantly different compared with controls with NGT; however, further studies revealed that four of the eight analyzed individual CpG units within the amplicon were significantly hypomethylated in T2DM samples compared with the NGT samples. This study demonstrated for the first time, to the best of our knowledge, that miR-375 is overexpressed in plasma in patients with T2DM, and this may be used as a novel biomarker to distinguish between patients with T2DM and healthy individuals. It was also demonstrated in this study that the miR-375 promoter is hypomethylated, in patients with T2DM, which may regulate the expression of miR-375 and contribute to the pathogenesis of T2DM.

摘要

最近的研究表明,miR-375(微小 RNA-375)启动子中的 DNA 甲基化在肿瘤发生过程中下调其表达。然而,miR-375 启动子的 CpG 甲基化是否也在 2 型糖尿病(T2DM)的发病机制中起作用尚不清楚。在这项研究中,分析了 T2DM 患者 miR-375 的表达水平和 CpG 甲基化状态。收集了 100 例 T2DM 患者和 100 例糖耐量正常(NGT)的健康对照者的血浆样本。使用定量聚合酶链反应(qPCR)检测 miR-375 的血浆水平,并使用 MassARRAY 光谱法测定 miR-375 启动子中 17 个 CpG 位点的甲基化状态。结果发现,与 NGT 对照组相比,T2DM 患者的 miR-375 血浆水平升高(P<0.05)。总体而言,与 NGT 对照组相比,T2DM 患者 miR-375 启动子的甲基化水平没有显著差异;然而,进一步的研究表明,在 T2DM 样本中,在分析的 8 个单个 CpG 单元中,有 4 个 CpG 单元明显低甲基化。本研究首次表明,miR-375 在 T2DM 患者的血浆中过度表达,这可能作为区分 T2DM 患者和健康个体的新型生物标志物。本研究还表明,在 T2DM 患者中,miR-375 启动子呈低甲基化状态,可能调节 miR-375 的表达,并有助于 T2DM 的发病机制。

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