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DNA Methylation in Alcohol Use Disorder

Excessive drinking damages the central nervous system of individuals and can even cause alcohol use disorder (AUD). AUD is regulated by both genetic and environmental factors. Genes determine susceptibility to alcohol, and the dysregulation of epigenome drives the abnormal transcription program and...

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Detalles Bibliográficos
Autores principales: Zheng, Qingmeng, Wang, Heng, Yan, An, Yin, Fangyuan, Qiao, Xiaomeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298675/
https://www.ncbi.nlm.nih.gov/pubmed/37373281
http://dx.doi.org/10.3390/ijms241210130
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author Zheng, Qingmeng
Wang, Heng
Yan, An
Yin, Fangyuan
Qiao, Xiaomeng
author_facet Zheng, Qingmeng
Wang, Heng
Yan, An
Yin, Fangyuan
Qiao, Xiaomeng
author_sort Zheng, Qingmeng
collection PubMed
description Excessive drinking damages the central nervous system of individuals and can even cause alcohol use disorder (AUD). AUD is regulated by both genetic and environmental factors. Genes determine susceptibility to alcohol, and the dysregulation of epigenome drives the abnormal transcription program and promotes the occurrence and development of AUD. DNA methylation is one of the earliest and most widely studied epigenetic mechanisms that can be inherited stably. In ontogeny, DNA methylation pattern is a dynamic process, showing differences and characteristics at different stages. DNA dysmethylation is prevalent in human cancer and alcohol-related psychiatric disorders, resulting in local hypermethylation and transcriptional silencing of related genes. Here, we summarize recent findings on the roles and regulatory mechanisms of DNA methylation, the development of methyltransferase inhibitors, methylation alteration during alcohol exposure at different stages of life, and possible therapeutic options for targeting methylation in human and animal studies.
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spelling pubmed-102986752023-06-28 DNA Methylation in Alcohol Use Disorder Zheng, Qingmeng Wang, Heng Yan, An Yin, Fangyuan Qiao, Xiaomeng Int J Mol Sci Review Excessive drinking damages the central nervous system of individuals and can even cause alcohol use disorder (AUD). AUD is regulated by both genetic and environmental factors. Genes determine susceptibility to alcohol, and the dysregulation of epigenome drives the abnormal transcription program and promotes the occurrence and development of AUD. DNA methylation is one of the earliest and most widely studied epigenetic mechanisms that can be inherited stably. In ontogeny, DNA methylation pattern is a dynamic process, showing differences and characteristics at different stages. DNA dysmethylation is prevalent in human cancer and alcohol-related psychiatric disorders, resulting in local hypermethylation and transcriptional silencing of related genes. Here, we summarize recent findings on the roles and regulatory mechanisms of DNA methylation, the development of methyltransferase inhibitors, methylation alteration during alcohol exposure at different stages of life, and possible therapeutic options for targeting methylation in human and animal studies. MDPI 2023-06-14 /pmc/articles/PMC10298675/ /pubmed/37373281 http://dx.doi.org/10.3390/ijms241210130 Text en © 2023 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
Zheng, Qingmeng
Wang, Heng
Yan, An
Yin, Fangyuan
Qiao, Xiaomeng
DNA Methylation in Alcohol Use Disorder
title DNA Methylation in Alcohol Use Disorder
title_full DNA Methylation in Alcohol Use Disorder
title_fullStr DNA Methylation in Alcohol Use Disorder
title_full_unstemmed DNA Methylation in Alcohol Use Disorder
title_short DNA Methylation in Alcohol Use Disorder
title_sort dna methylation in alcohol use disorder
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298675/
https://www.ncbi.nlm.nih.gov/pubmed/37373281
http://dx.doi.org/10.3390/ijms241210130
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