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Role of Epigenetics in Type 2 Diabetes and Obesity
Epigenetic marks the genome by DNA methylation, histone modification or non-coding RNAs. Epigenetic marks instruct cells to respond reversibly to environmental cues and keep the specific gene expression stable throughout life. In this review, we concentrate on DNA methylation, the mechanism often as...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8393970/ https://www.ncbi.nlm.nih.gov/pubmed/34440181 http://dx.doi.org/10.3390/biomedicines9080977 |
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author | Capparelli, Rosanna Iannelli, Domenico |
author_facet | Capparelli, Rosanna Iannelli, Domenico |
author_sort | Capparelli, Rosanna |
collection | PubMed |
description | Epigenetic marks the genome by DNA methylation, histone modification or non-coding RNAs. Epigenetic marks instruct cells to respond reversibly to environmental cues and keep the specific gene expression stable throughout life. In this review, we concentrate on DNA methylation, the mechanism often associated with transgenerational persistence and for this reason frequently used in the clinic. A large study that included data from 10,000 blood samples detected 187 methylated sites associated with body mass index (BMI). The same study demonstrates that altered methylation results from obesity (OB). In another study the combined genetic and epigenetic analysis allowed us to understand the mechanism associating hepatic insulin resistance and non-alcoholic disease in Type 2 Diabetes (T2D) patients. The study underlines the therapeutic potential of epigenetic studies. We also account for seemingly contradictory results associated with epigenetics. |
format | Online Article Text |
id | pubmed-8393970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83939702021-08-28 Role of Epigenetics in Type 2 Diabetes and Obesity Capparelli, Rosanna Iannelli, Domenico Biomedicines Review Epigenetic marks the genome by DNA methylation, histone modification or non-coding RNAs. Epigenetic marks instruct cells to respond reversibly to environmental cues and keep the specific gene expression stable throughout life. In this review, we concentrate on DNA methylation, the mechanism often associated with transgenerational persistence and for this reason frequently used in the clinic. A large study that included data from 10,000 blood samples detected 187 methylated sites associated with body mass index (BMI). The same study demonstrates that altered methylation results from obesity (OB). In another study the combined genetic and epigenetic analysis allowed us to understand the mechanism associating hepatic insulin resistance and non-alcoholic disease in Type 2 Diabetes (T2D) patients. The study underlines the therapeutic potential of epigenetic studies. We also account for seemingly contradictory results associated with epigenetics. MDPI 2021-08-08 /pmc/articles/PMC8393970/ /pubmed/34440181 http://dx.doi.org/10.3390/biomedicines9080977 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Capparelli, Rosanna Iannelli, Domenico Role of Epigenetics in Type 2 Diabetes and Obesity |
title | Role of Epigenetics in Type 2 Diabetes and Obesity |
title_full | Role of Epigenetics in Type 2 Diabetes and Obesity |
title_fullStr | Role of Epigenetics in Type 2 Diabetes and Obesity |
title_full_unstemmed | Role of Epigenetics in Type 2 Diabetes and Obesity |
title_short | Role of Epigenetics in Type 2 Diabetes and Obesity |
title_sort | role of epigenetics in type 2 diabetes and obesity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8393970/ https://www.ncbi.nlm.nih.gov/pubmed/34440181 http://dx.doi.org/10.3390/biomedicines9080977 |
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