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DNA Methylation in Nonalcoholic Fatty Liver Disease

Nonalcoholic fatty liver disease (NAFLD) is a widespread hepatic disorder in the United States and other Westernized countries. Nonalcoholic steatohepatitis (NASH), an advanced stage of NAFLD, can progress to end-stage liver disease, including cirrhosis and liver cancer. Poor understanding of mechan...

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Autores principales: Hyun, Jeongeun, Jung, Youngmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662478/
https://www.ncbi.nlm.nih.gov/pubmed/33143364
http://dx.doi.org/10.3390/ijms21218138
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author Hyun, Jeongeun
Jung, Youngmi
author_facet Hyun, Jeongeun
Jung, Youngmi
author_sort Hyun, Jeongeun
collection PubMed
description Nonalcoholic fatty liver disease (NAFLD) is a widespread hepatic disorder in the United States and other Westernized countries. Nonalcoholic steatohepatitis (NASH), an advanced stage of NAFLD, can progress to end-stage liver disease, including cirrhosis and liver cancer. Poor understanding of mechanisms underlying NAFLD progression from simple steatosis to NASH has limited the development of effective therapies and biomarkers. An accumulating body of studies has suggested the importance of DNA methylation, which plays pivotal roles in NAFLD pathogenesis. DNA methylation signatures that can affect gene expression are influenced by environmental and lifestyle experiences such as diet, obesity, and physical activity and are reversible. Hence, DNA methylation signatures and modifiers in NAFLD may provide the basis for developing biomarkers indicating the onset and progression of NAFLD and therapeutics for NAFLD. Herein, we review an update on the recent findings in DNA methylation signatures and their roles in the pathogenesis of NAFLD and broaden people’s perspectives on potential DNA methylation-related treatments and biomarkers for NAFLD.
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spelling pubmed-76624782020-11-14 DNA Methylation in Nonalcoholic Fatty Liver Disease Hyun, Jeongeun Jung, Youngmi Int J Mol Sci Review Nonalcoholic fatty liver disease (NAFLD) is a widespread hepatic disorder in the United States and other Westernized countries. Nonalcoholic steatohepatitis (NASH), an advanced stage of NAFLD, can progress to end-stage liver disease, including cirrhosis and liver cancer. Poor understanding of mechanisms underlying NAFLD progression from simple steatosis to NASH has limited the development of effective therapies and biomarkers. An accumulating body of studies has suggested the importance of DNA methylation, which plays pivotal roles in NAFLD pathogenesis. DNA methylation signatures that can affect gene expression are influenced by environmental and lifestyle experiences such as diet, obesity, and physical activity and are reversible. Hence, DNA methylation signatures and modifiers in NAFLD may provide the basis for developing biomarkers indicating the onset and progression of NAFLD and therapeutics for NAFLD. Herein, we review an update on the recent findings in DNA methylation signatures and their roles in the pathogenesis of NAFLD and broaden people’s perspectives on potential DNA methylation-related treatments and biomarkers for NAFLD. MDPI 2020-10-30 /pmc/articles/PMC7662478/ /pubmed/33143364 http://dx.doi.org/10.3390/ijms21218138 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hyun, Jeongeun
Jung, Youngmi
DNA Methylation in Nonalcoholic Fatty Liver Disease
title DNA Methylation in Nonalcoholic Fatty Liver Disease
title_full DNA Methylation in Nonalcoholic Fatty Liver Disease
title_fullStr DNA Methylation in Nonalcoholic Fatty Liver Disease
title_full_unstemmed DNA Methylation in Nonalcoholic Fatty Liver Disease
title_short DNA Methylation in Nonalcoholic Fatty Liver Disease
title_sort dna methylation in nonalcoholic fatty liver disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662478/
https://www.ncbi.nlm.nih.gov/pubmed/33143364
http://dx.doi.org/10.3390/ijms21218138
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