Gender-dependent miR-375 promoter methylation and the risk of type 2 diabetes

被引:11
作者
Cheng, Jia [1 ,2 ]
Wang, Lingyan [3 ]
Xu, Leiting [1 ]
Wang, Hongwei [4 ]
Liu, Panpan [1 ]
Bu, Shizhong [5 ]
Ye, Meng [6 ]
Zhang, Lina [1 ]
Wang, Qinwen [1 ]
Duan, Shiwei [1 ]
机构
[1] Ningbo Univ, Sch Med, Zhejiang Prov Key Lab Pathophysiol, Ningbo 315211, Zhejiang, Peoples R China
[2] Ningbo Kangning Hosp, Dept Clin Med, Ningbo 315201, Zhejiang, Peoples R China
[3] Ningbo 2 Hosp, Bank Blood Prod, Ningbo 315010, Zhejiang, Peoples R China
[4] Univ Chicago, Pritzker Sch Med, Sect Endocrinol, Chicago, IL 60637 USA
[5] Ningbo Univ, Sch Med, Ctr Diabet, Ningbo 315211, Zhejiang, Peoples R China
[6] Ningbo Univ, Sch Med, Affiliated Hosp, Dept Endocrinol, Ningbo 315000, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
type; 2; diabetes; miR-375; DNA methylation; promoter; GENE; MICRORNAS; ESTROGEN; EXPRESSION;
D O I
10.3892/etm.2013.1069
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Promoter DNA methylation may reflect the interaction between genetic background and environmental factors in the development of metabolic disorders, including type 2 diabetes (T2D). As an epigenetic factor of T2D, miR-375 plays an important role in the functional accommodation of islet cells. In the present study, we investigated the association of promoter DNA methylation of the miR-375 gene with the risk of T2D. Using bisulfite pyrosequencing technology, the DNA methylation levels of eight CpG dinucleotides on the miR-375 promoter were measured in 48 T2D cases and 48 healthy controls. The majority of CpGs (with the exception of CpG7) had significantly higher methylation levels in women compared with those in men (P<0.05). The methylation levels of the eight CpGs were significantly correlated with each other (P<0.001). No significant association between miR-375 gene promoter methylation and the risk of T2D was identified (P=0.417). Similar results were observed in the breakdown analysis by gender (men, P=0.844; women, P=0.234). In addition, although a correlation between the CpG8 methylation level of miR-375 and total triglyceride level was identified in women (P=0.009), DNA methylation of the majority of CpGs in the miR-375 gene promoter was not associated with the clinical metabolic features of the individuals.
引用
收藏
页码:1687 / 1692
页数:6
相关论文
共 23 条
[11]   Insulin Gene Expression Is Regulated by DNA Methylation [J].
Kuroda, Akio ;
Rauch, Tibor A. ;
Todorov, Ivan ;
Ku, Hsun Teresa ;
Al-Abdullah, Ismail H. ;
Kandeel, Fouad ;
Mullen, Yoko ;
Pfeifer, Gerd P. ;
Ferreri, Kevin .
PLOS ONE, 2009, 4 (09)
[12]   THE C-ELEGANS HETEROCHRONIC GENE LIN-4 ENCODES SMALL RNAS WITH ANTISENSE COMPLEMENTARITY TO LIN-14 [J].
LEE, RC ;
FEINBAUM, RL ;
AMBROS, V .
CELL, 1993, 75 (05) :843-854
[13]   Estrogen and progesterone receptor status affect genome-wide DNA methylation profile in breast cancer [J].
Li, Lian ;
Lee, Kyoung-Mu ;
Han, Wonshik ;
Choi, Ji-Yeob ;
Lee, Ji-Young ;
Kang, Gyeong Hoon ;
Park, Sue Kyung ;
Noh, Dong-Young ;
Yoo, Keun-Young ;
Kang, Daehee .
HUMAN MOLECULAR GENETICS, 2010, 19 (21) :4273-4277
[14]   MicroRNA-375 promotes 3T3-L1 adipocyte differentiation through modulation of extracellular signal-regulated kinase signalling [J].
Ling, Hong-Yan ;
Wen, Ge-Bo ;
Feng, Shui-Dong ;
Tuo, Qin-Hui ;
Ou, He-Sheng ;
Yao, Chao Hua ;
Zhu, Bing-Yang ;
Gao, Zhi-Ping ;
Zhang, Liang ;
Liao, Duan-Fang .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2011, 38 (04) :239-246
[15]   miR-375 maintains normal pancreatic α- and β-cell mass [J].
Poy, Matthew N. ;
Hausser, Jean ;
Trajkovski, Mirko ;
Braun, Matthias ;
Collins, Stephan ;
Rorsman, Patrik ;
Zavolan, Mihaela ;
Stoffel, Markus .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (14) :5813-5818
[16]   A pancreatic islet-specific microRNA regulates insulin secretion [J].
Poy, MN ;
Eliasson, L ;
Krutzfeldt, J ;
Kuwajima, S ;
Ma, XS ;
MacDonald, PE ;
Pfeffer, S ;
Tuschl, T ;
Rajewsky, N ;
Rorsman, P ;
Stoffel, M .
NATURE, 2004, 432 (7014) :226-230
[17]   Role of microRNAs in diabetes and its cardiovascular complications [J].
Shantikumar, Saran ;
Caporali, Andrea ;
Emanueli, Costanza .
CARDIOVASCULAR RESEARCH, 2012, 93 (04) :583-593
[18]   Global estimates of the prevalence of diabetes for 2010 and 2030 [J].
Shaw, J. E. ;
Sicree, R. A. ;
Zimmet, P. Z. .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2010, 87 (01) :4-14
[19]   Mechanisms of epigenetic silencing of the Rassf1a gene during estrogen-induced breast carcinogenesis in ACI rats [J].
Starlard-Davenport, Athena ;
Tryndyak, Volodymyr P. ;
James, Smitha R. ;
Karpf, Adam R. ;
Latendresse, John R. ;
Beland, Frederick A. ;
Pogribny, Igor P. .
CARCINOGENESIS, 2010, 31 (03) :376-381
[20]   DNA methylation profiling identifies epigenetic dysregulation in pancreatic islets from type 2 diabetic patients [J].
Volkmar, Michael ;
Dedeurwaerder, Sarah ;
Cunha, Daniel A. ;
Ndlovu, Matladi N. ;
Defrance, Matthieu ;
Deplus, Rachel ;
Calonne, Emilie ;
Volkmar, Ute ;
Igoillo-Esteve, Mariana ;
Naamane, Najib ;
Del Guerra, Silvia ;
Masini, Matilde ;
Bugliani, Marco ;
Marchetti, Piero ;
Cnop, Miriam ;
Eizirik, Decio L. ;
Fuks, Francois .
EMBO JOURNAL, 2012, 31 (06) :1405-1426