Epigenetics and Liver FibrosisSummary
Liver fibrosis arises because prolonged injury combined with excessive scar deposition within hepatic parenchyma arising from overactive wound healing response mediated by activated myofibroblasts. Fibrosis is the common end point for any type of chronic liver injury including alcoholic liver diseas...
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2017-07-01
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doaj-42e8ca1e30be469194cdb0ea4243da122020-11-24T23:50:24ZengElsevierCellular and Molecular Gastroenterology and Hepatology2352-345X2017-07-0141125134Epigenetics and Liver FibrosisSummaryEva Moran-Salvador0Jelena Mann1Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Framlington Place, Newcastle upon Tyne, United KingdomCorrespondence Address correspondence to: Jelena Mann, PhD, Institute of Cellular Medicine, Faculty of Medical Sciences, 4th Floor, William Leech Building, Newcastle University, Framlington Place, Newcastle upon Tyne, NE2 4HH United Kingdom. fax: +44-191-208-0723.; Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Framlington Place, Newcastle upon Tyne, United KingdomLiver fibrosis arises because prolonged injury combined with excessive scar deposition within hepatic parenchyma arising from overactive wound healing response mediated by activated myofibroblasts. Fibrosis is the common end point for any type of chronic liver injury including alcoholic liver disease, nonalcoholic fatty liver disease, viral hepatitis, and cholestatic liver diseases. Although genetic influences are important, it is epigenetic mechanisms that have been shown to orchestrate many aspects of fibrogenesis in the liver. New discoveries in the field are leading toward the development of epigenetic biomarkers and targeted therapies. This review considers epigenetic mechanisms as well as recent advances in epigenetic programming in the context of hepatic fibrosis. Keywords: Liver Fibrosis, Epigenetics, DNA Methylation, Histone Modifications, Chronic Liver Diseasehttp://www.sciencedirect.com/science/article/pii/S2352345X17300814 |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Eva Moran-Salvador Jelena Mann |
spellingShingle |
Eva Moran-Salvador Jelena Mann Epigenetics and Liver FibrosisSummary Cellular and Molecular Gastroenterology and Hepatology |
author_facet |
Eva Moran-Salvador Jelena Mann |
author_sort |
Eva Moran-Salvador |
title |
Epigenetics and Liver FibrosisSummary |
title_short |
Epigenetics and Liver FibrosisSummary |
title_full |
Epigenetics and Liver FibrosisSummary |
title_fullStr |
Epigenetics and Liver FibrosisSummary |
title_full_unstemmed |
Epigenetics and Liver FibrosisSummary |
title_sort |
epigenetics and liver fibrosissummary |
publisher |
Elsevier |
series |
Cellular and Molecular Gastroenterology and Hepatology |
issn |
2352-345X |
publishDate |
2017-07-01 |
description |
Liver fibrosis arises because prolonged injury combined with excessive scar deposition within hepatic parenchyma arising from overactive wound healing response mediated by activated myofibroblasts. Fibrosis is the common end point for any type of chronic liver injury including alcoholic liver disease, nonalcoholic fatty liver disease, viral hepatitis, and cholestatic liver diseases. Although genetic influences are important, it is epigenetic mechanisms that have been shown to orchestrate many aspects of fibrogenesis in the liver. New discoveries in the field are leading toward the development of epigenetic biomarkers and targeted therapies. This review considers epigenetic mechanisms as well as recent advances in epigenetic programming in the context of hepatic fibrosis. Keywords: Liver Fibrosis, Epigenetics, DNA Methylation, Histone Modifications, Chronic Liver Disease |
url |
http://www.sciencedirect.com/science/article/pii/S2352345X17300814 |
work_keys_str_mv |
AT evamoransalvador epigeneticsandliverfibrosissummary AT jelenamann epigeneticsandliverfibrosissummary |
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1725478663959347200 |