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Gender-dependent miR-375 promoter methylation and the risk of type 2 diabetes
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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3702700/ https://www.ncbi.nlm.nih.gov/pubmed/23837055 http://dx.doi.org/10.3892/etm.2013.1069 |
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author | CHENG, JIA WANG, LINGYAN XU, LEITING WANG, HONGWEI LIU, PANPAN BU, SHIZHONG YE, MENG ZHANG, LINA WANG, QINWEN DUAN, SHIWEI |
author_facet | CHENG, JIA WANG, LINGYAN XU, LEITING WANG, HONGWEI LIU, PANPAN BU, SHIZHONG YE, MENG ZHANG, LINA WANG, QINWEN DUAN, SHIWEI |
author_sort | CHENG, JIA |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3702700 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-37027002013-07-08 Gender-dependent miR-375 promoter methylation and the risk of type 2 diabetes CHENG, JIA WANG, LINGYAN XU, LEITING WANG, HONGWEI LIU, PANPAN BU, SHIZHONG YE, MENG ZHANG, LINA WANG, QINWEN DUAN, SHIWEI Exp Ther Med Articles 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. D.A. Spandidos 2013-06 2013-04-18 /pmc/articles/PMC3702700/ /pubmed/23837055 http://dx.doi.org/10.3892/etm.2013.1069 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles CHENG, JIA WANG, LINGYAN XU, LEITING WANG, HONGWEI LIU, PANPAN BU, SHIZHONG YE, MENG ZHANG, LINA WANG, QINWEN DUAN, SHIWEI Gender-dependent miR-375 promoter methylation and the risk of type 2 diabetes |
title | Gender-dependent miR-375 promoter methylation and the risk of type 2 diabetes |
title_full | Gender-dependent miR-375 promoter methylation and the risk of type 2 diabetes |
title_fullStr | Gender-dependent miR-375 promoter methylation and the risk of type 2 diabetes |
title_full_unstemmed | Gender-dependent miR-375 promoter methylation and the risk of type 2 diabetes |
title_short | Gender-dependent miR-375 promoter methylation and the risk of type 2 diabetes |
title_sort | gender-dependent mir-375 promoter methylation and the risk of type 2 diabetes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3702700/ https://www.ncbi.nlm.nih.gov/pubmed/23837055 http://dx.doi.org/10.3892/etm.2013.1069 |
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