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本文引用的文献

1
Association of 5-hydroxymethylation and 5-methylation of DNA cytosine with tissue-specific gene expression.DNA胞嘧啶的5-羟甲基化和5-甲基化与组织特异性基因表达的关联。
Epigenetics. 2017 Feb;12(2):123-138. doi: 10.1080/15592294.2016.1265713. Epub 2016 Dec 2.
2
Worldwide trends in diabetes since 1980: a pooled analysis of 751 population-based studies with 4.4 million participants.1980年以来全球糖尿病趋势:对751项基于人群的研究进行的汇总分析,涉及440万参与者。
Lancet. 2016 Apr 9;387(10027):1513-1530. doi: 10.1016/S0140-6736(16)00618-8. Epub 2016 Apr 6.
3
Methylation of insulin DNA in response to proinflammatory cytokines during the progression of autoimmune diabetes in NOD mice.在非肥胖糖尿病(NOD)小鼠自身免疫性糖尿病进展过程中,胰岛素DNA对促炎细胞因子的甲基化反应。
Diabetologia. 2016 May;59(5):1021-9. doi: 10.1007/s00125-016-3897-4. Epub 2016 Feb 24.
4
Hypomethylation within gene promoter regions and type 1 diabetes in discordant monozygotic twins.基因启动子区域的低甲基化与不一致性单卵双胞胎中的1型糖尿病
J Autoimmun. 2016 Apr;68:23-9. doi: 10.1016/j.jaut.2015.12.003. Epub 2016 Jan 9.
5
Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation.对两个组织进行的群体全基因组亚硫酸氢盐测序表明,环境是人类甲基化组变异的主要来源。
Genome Biol. 2015 Dec 23;16:290. doi: 10.1186/s13059-015-0856-1.
6
Validation of a DNA methylation microarray for 850,000 CpG sites of the human genome enriched in enhancer sequences.验证一种针对人类基因组中富含增强子序列的 850,000 个 CpG 位点的 DNA 甲基化微阵列。
Epigenomics. 2016 Mar;8(3):389-99. doi: 10.2217/epi.15.114. Epub 2015 Dec 17.
7
Elevations in Circulating Methylated and Unmethylated Preproinsulin DNA in New-Onset Type 1 Diabetes.新发1型糖尿病患者循环中甲基化和未甲基化前胰岛素原DNA水平升高。
Diabetes. 2015 Nov;64(11):3867-72. doi: 10.2337/db15-0430. Epub 2015 Jul 27.
8
DNA methylation as a diagnostic and therapeutic target in the battle against Type 2 diabetes.DNA 甲基化作为 2 型糖尿病防治的诊断和治疗靶点。
Epigenomics. 2015;7(3):451-60. doi: 10.2217/epi.15.7.
9
DNA methylation profiles in placenta and its association with gestational diabetes mellitus.胎盘的DNA甲基化图谱及其与妊娠期糖尿病的关联。
Exp Clin Endocrinol Diabetes. 2015 May;123(5):282-8. doi: 10.1055/s-0034-1398666. Epub 2015 Apr 21.
10
The potential use of DNA methylation biomarkers to identify risk and progression of type 2 diabetes.DNA甲基化生物标志物在识别2型糖尿病风险及病情进展方面的潜在用途。
Front Endocrinol (Lausanne). 2015 Mar 30;6:43. doi: 10.3389/fendo.2015.00043. eCollection 2015.

DNA甲基化及其在糖尿病发病机制中的作用。

DNA methylation and its role in the pathogenesis of diabetes.

作者信息

Bansal Amita, Pinney Sara E

机构信息

Center for Research on Reproduction and Women's Health, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Center of Excellence in Environmental Toxicology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Pediatr Diabetes. 2017 May;18(3):167-177. doi: 10.1111/pedi.12521.

DOI:10.1111/pedi.12521
PMID:28401680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5394941/
Abstract

Although the factors responsible for the recent increase in the prevalence of diabetes worldwide are not entirely known, the morbidity associated with this disease results in substantial health and economic burden on society. Epigenetic modifications, including DNA methylation have been identified as one mechanism by which the environment interacts with the genome and there is evidence that alterations in DNA methylation may contribute to the increased prevalence of both type 1 and type 2 diabetes. This review provides a summary of DNA methylation and its role in gene regulation, and includes descriptions of various techniques to measure site-specific and genome-wide DNA methylation changes. In addition, we review current literature highlighting the complex relationship between DNA methylation, gene expression, and the development of diabetes and related complications. In studies where both DNA methylation and gene expression changes were reported, DNA methylation status had a strong inverse correlation with gene expression, suggesting that this interaction may be a potential future therapeutic target. We highlight the emerging use of genome-wide DNA methylation profiles as a biomarker to predict patients at risk of developing diabetes or specific complications of diabetes. The development of a predictive model that incorporates both genetic sequencing and DNA methylation data may be an effective diagnostic approach for all types of diabetes and could lead to additional innovative therapies.

摘要

尽管导致全球糖尿病患病率近期上升的因素尚不完全清楚,但这种疾病所带来的发病率给社会造成了巨大的健康和经济负担。包括DNA甲基化在内的表观遗传修饰已被确定为环境与基因组相互作用的一种机制,并且有证据表明DNA甲基化的改变可能导致1型和2型糖尿病患病率的上升。本综述总结了DNA甲基化及其在基因调控中的作用,并介绍了测量位点特异性和全基因组DNA甲基化变化的各种技术。此外,我们回顾了当前的文献,突出了DNA甲基化、基因表达与糖尿病及其相关并发症发展之间的复杂关系。在报告了DNA甲基化和基因表达变化的研究中,DNA甲基化状态与基因表达呈强烈的负相关,这表明这种相互作用可能是未来潜在的治疗靶点。我们强调全基因组DNA甲基化谱作为一种生物标志物在预测糖尿病或糖尿病特定并发症风险患者中的新兴应用。结合基因测序和DNA甲基化数据的预测模型的开发可能是针对所有类型糖尿病的一种有效诊断方法,并可能带来更多创新疗法。