Epigenetic regulation of microRNA-375 and its role as DNA epigenetic marker of type 2 diabetes mellitus in Chinese Han population

被引:0
作者
Yin, Liang [1 ,2 ]
Zhang, Ting [3 ]
Wei, Yu [4 ]
Cai, Wei-Juan [5 ]
Feng, Gang [1 ,2 ]
Chang, Xiang-Yun [1 ,2 ]
Sun, Kan [1 ,2 ]
机构
[1] Shihezi Univ, Sch Med, Affiliated Hosp 1, Dept Endocrinol & Metab, Shihezi 832002, Xinjiang, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Endocrinol & Metab, Tongji Med Coll, Wuhan 43000, Hubei, Peoples R China
[3] Shihezi Univ, Sch Med, Affiliated Hosp 1, Dept Orthoped Surg, Shihezi 832002, Xinjiang, Peoples R China
[4] Shihezi Univ, Sch Med, Affiliated Hosp 1, Clin Lab, Shihezi 832002, Xinjiang, Peoples R China
[5] Shihezi Univ, Sch Med, Affiliated Hosp 1, Cent Lab, Shihezi 832002, Xinjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Type 2 diabetes mellitus; DNA methylation; microRNA-375; biomarker; BETA-CELL DEFICIT; INSULIN-SECRETION; EXPRESSION; CANCER; METHYLATION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epigenetics may affect the susceptibility for type 2 diabetes mellitus (T2DM). Previously, our studies have shown that the hypomethylation of human miR-375 promoter may contribute to the pathogenesis of T2DM. However, the methylation pattern of miR-375 promoter in T2DM is not yet fully understood. In this study, the DNA methylation status of the different region of miR-375 promoter in Chinese Han population with T2DM were explored. 100 Han patients with T2DM and 100 Han healthy controls with normal glucose tolerance (NGT) were collected. Then the transcription level of pre-miR-375 and mature miR-375 were examined using quantitative real-time PCR and the methylation status of 27 CpG sites in the miR-375 promoter was determined by MassARRAY Spectrometry. The relative expression of mature miR-375 was shown as fold difference relative to miR-16 (3.0-fold, P=0.0260) and pre-miR-375 was markedly unregulated (2.6-fold, P=0.0415) in Han T2DM samples. Aberrant methylation was significantly higher within the amplicon of the miR-375 promoter in T2DMs than in NGTs, an average of 10.27% and 7.24% (P=0.0004; Figure 3A), respectively. Further, one CpG unit (CpG_26.27) was significantly hypermethylated in T2DM samples compared with NGT. Together, our results highlights for the first time that aberrant hypermethylation is a common event in Han T2DM, suggesting that the aberrant methylation of the CpG sites within miR-375 promoter may serve as a potential candidate biomarker for T2DM in the Chinese Han population.
引用
收藏
页码:11986 / 11994
页数:9
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