EZH2 as a Potential Target for NAFLD Therapy

Non-alcoholic fatty liver disease (NAFLD) is a complex disease that is affected by genetic predisposition and epigenetic modification. Deregulation of epigenetic pathways is now recognized as a frequent event in NAFLD, and understanding the mechanistic roles of these epigenetic factors may lead to n...

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Main Authors: Hyun Jung Lim, Mirang Kim
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/22/8617
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author Hyun Jung Lim
Mirang Kim
author_facet Hyun Jung Lim
Mirang Kim
author_sort Hyun Jung Lim
collection DOAJ
description Non-alcoholic fatty liver disease (NAFLD) is a complex disease that is affected by genetic predisposition and epigenetic modification. Deregulation of epigenetic pathways is now recognized as a frequent event in NAFLD, and understanding the mechanistic roles of these epigenetic factors may lead to new strategies for NAFLD treatment. Enhancer of zeste homolog 2 (EZH2) catalyzes methylation on Lys 27 of histone H3, which leads to chromatin compaction and gene silencing. EZH2 regulates embryonic development and cell lineage determination and is related to many human diseases. Recent studies show that EZH2 has critical roles in liver development, homeostasis, and regeneration. Moreover, aberrant activation of EZH2 promotes NAFLD progression. Several EZH2 inhibitors have been developed and studied both in vitro and in clinical trials. In this review, we summarize our current understanding of the role of EZH2 in NAFLD and highlight its potential as a novel therapeutic target for NAFLD treatment.
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spelling doaj.art-79b82841de1a48759f73f5f569caa18a2023-11-20T21:04:19ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-11-012122861710.3390/ijms21228617EZH2 as a Potential Target for NAFLD TherapyHyun Jung Lim0Mirang Kim1Personalized Genomic Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, KoreaPersonalized Genomic Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon 34141, KoreaNon-alcoholic fatty liver disease (NAFLD) is a complex disease that is affected by genetic predisposition and epigenetic modification. Deregulation of epigenetic pathways is now recognized as a frequent event in NAFLD, and understanding the mechanistic roles of these epigenetic factors may lead to new strategies for NAFLD treatment. Enhancer of zeste homolog 2 (EZH2) catalyzes methylation on Lys 27 of histone H3, which leads to chromatin compaction and gene silencing. EZH2 regulates embryonic development and cell lineage determination and is related to many human diseases. Recent studies show that EZH2 has critical roles in liver development, homeostasis, and regeneration. Moreover, aberrant activation of EZH2 promotes NAFLD progression. Several EZH2 inhibitors have been developed and studied both in vitro and in clinical trials. In this review, we summarize our current understanding of the role of EZH2 in NAFLD and highlight its potential as a novel therapeutic target for NAFLD treatment.https://www.mdpi.com/1422-0067/21/22/8617epigeneticsEZH2NAFLDNASHliver fibrosis
spellingShingle Hyun Jung Lim
Mirang Kim
EZH2 as a Potential Target for NAFLD Therapy
International Journal of Molecular Sciences
epigenetics
EZH2
NAFLD
NASH
liver fibrosis
title EZH2 as a Potential Target for NAFLD Therapy
title_full EZH2 as a Potential Target for NAFLD Therapy
title_fullStr EZH2 as a Potential Target for NAFLD Therapy
title_full_unstemmed EZH2 as a Potential Target for NAFLD Therapy
title_short EZH2 as a Potential Target for NAFLD Therapy
title_sort ezh2 as a potential target for nafld therapy
topic epigenetics
EZH2
NAFLD
NASH
liver fibrosis
url https://www.mdpi.com/1422-0067/21/22/8617
work_keys_str_mv AT hyunjunglim ezh2asapotentialtargetfornafldtherapy
AT mirangkim ezh2asapotentialtargetfornafldtherapy