Literature DB >> 22245903

Clinical evidence for the regression of liver fibrosis.

Elizabeth L Ellis1, Derek A Mann.   

Abstract

Fibrosis is a common pathological process for the majority of liver diseases which in a significant minority of patients leads to end-stage cirrhosis and/or hepatocellular carcinoma. Data emerging from small rodent models of chronic liver disease have demonstrated that fibrotic extracellular matrix can be remodelled and near-normal hepatic architecture regenerated upon cessation of injury. Moreover, regression of liver fibrosis in these model systems can be stimulated with drugs that target the activities of fibrogenic hepatic stellate cells. These findings are exciting as they suggest that established fibrosis is susceptible to regression and possibly even reversion. Alongside these experimental studies is a growing body of clinical data that suggest regression of fibrosis may also occur in liver disease patients for whom an effective treatment is available for their underlying liver injury. This paper provides an up-to-date review of the currently available clinical data and also considers technical caveats that highlight the need for caution in establishing a new dogma that human liver fibrosis is reversible. Copyright Â
© 2012 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 22245903     DOI: 10.1016/j.jhep.2011.09.024

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  134 in total

1.  Mouse Models of Liver Fibrosis.

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2.  Liver shape analysis using partial least squares regression-based statistical shape model: application for understanding and staging of liver fibrosis.

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3.  Effect of reversine on cell cycle, apoptosis, and activation of hepatic stellate cells.

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4.  Hepatitis: Long-term therapy of chronic hepatitis B reverses cirrhosis.

Authors:  Anna Suk-Fong Lok
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Review 5.  Hepatic stellate cells in liver development, regeneration, and cancer.

Authors:  Chunyue Yin; Kimberley J Evason; Kinji Asahina; Didier Y R Stainier
Journal:  J Clin Invest       Date:  2013-05-01       Impact factor: 14.808

6.  Kinetin inhibits proliferation of hepatic stellate cells by interrupting cell cycle and induces apoptosis by down-regulating ratio of Bcl-2/Bax.

Authors:  Zhen-Gang Zhang; Jie Zou; Ying Huang; Liang Wu
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7.  Neutrophils contribute to spontaneous resolution of liver inflammation and fibrosis via microRNA-223.

Authors:  Carolina Jimenez Calvente; Masahiko Tameda; Casey D Johnson; Hana Del Pilar; Yun Chin Lin; Nektaria Adronikou; Xavier De Mollerat Du Jeu; Cristina Llorente; Josh Boyer; Ariel E Feldstein
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8.  Multiplex protein analysis to determine fibrosis stage and progression in patients with chronic hepatitis C.

Authors:  Keyur Patel; Katja S Remlinger; Terence G Walker; Peter Leitner; Joseph E Lucas; Stephen D Gardner; John G McHutchison; Will Irving; Indra Neil Guha
Journal:  Clin Gastroenterol Hepatol       Date:  2014-05-09       Impact factor: 11.382

9.  Diallyl trisulfide attenuates carbon tetrachloride-caused liver injury and fibrogenesis and reduces hepatic oxidative stress in rats.

Authors:  Xiaojing Zhu; Feng Zhang; Liang Zhou; Desong Kong; Li Chen; Yin Lu; Shizhong Zheng
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2014-02-21       Impact factor: 3.000

Review 10.  Cellular and molecular mechanisms in the pathogenesis of liver fibrosis: An update.

Authors:  Gülsüm Özlem Elpek
Journal:  World J Gastroenterol       Date:  2014-06-21       Impact factor: 5.742

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