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Distinct cellular responses differentiating alcohol- and hepatitis C virus-induced liver cirrhosis

BACKGROUND: Little is known at the molecular level concerning the differences and/or similarities between alcohol and hepatitis C virus induced liver disease. Global transcriptional profiling using oligonucleotide microarrays was therefore performed on liver biopsies from patients with cirrhosis cau...

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Autores principales: Lederer, Sharon L, Walters, Kathie-Anne, Proll, Sean, Paeper, Bryan, Robinzon, Shahar, Boix, Loreto, Fausto, Nelson, Bruix, Jordi, Katze, Michael G
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1676004/
https://www.ncbi.nlm.nih.gov/pubmed/17121680
http://dx.doi.org/10.1186/1743-422X-3-98
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author Lederer, Sharon L
Walters, Kathie-Anne
Proll, Sean
Paeper, Bryan
Robinzon, Shahar
Boix, Loreto
Fausto, Nelson
Bruix, Jordi
Katze, Michael G
author_facet Lederer, Sharon L
Walters, Kathie-Anne
Proll, Sean
Paeper, Bryan
Robinzon, Shahar
Boix, Loreto
Fausto, Nelson
Bruix, Jordi
Katze, Michael G
author_sort Lederer, Sharon L
collection PubMed
description BACKGROUND: Little is known at the molecular level concerning the differences and/or similarities between alcohol and hepatitis C virus induced liver disease. Global transcriptional profiling using oligonucleotide microarrays was therefore performed on liver biopsies from patients with cirrhosis caused by either chronic alcohol consumption or chronic hepatitis C virus (HCV). RESULTS: Global gene expression patterns varied significantly depending upon etiology of liver disease, with a greater number of differentially regulated genes seen in HCV-infected patients. Many of the gene expression changes specifically observed in HCV-infected cirrhotic livers were expectedly associated with activation of the innate antiviral immune response. We also compared severity (CTP class) of cirrhosis for each etiology and identified gene expression patterns that differentiated ethanol-induced cirrhosis by class. CTP class A ethanol-cirrhotic livers showed unique expression patterns for genes implicated in the inflammatory response, including those related to macrophage activation and migration, as well as lipid metabolism and oxidative stress genes. CONCLUSION: Stages of liver cirrhosis could be differentiated based on gene expression patterns in ethanol-induced, but not HCV-induced, disease. In addition to genes specifically regulating the innate antiviral immune response, mechanisms responsible for differentiating chronic liver damage due to HCV or ethanol may be closely related to regulation of lipid metabolism and to effects of macrophage activation on deposition of extracellular matrix components.
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spelling pubmed-16760042006-12-01 Distinct cellular responses differentiating alcohol- and hepatitis C virus-induced liver cirrhosis Lederer, Sharon L Walters, Kathie-Anne Proll, Sean Paeper, Bryan Robinzon, Shahar Boix, Loreto Fausto, Nelson Bruix, Jordi Katze, Michael G Virol J Research BACKGROUND: Little is known at the molecular level concerning the differences and/or similarities between alcohol and hepatitis C virus induced liver disease. Global transcriptional profiling using oligonucleotide microarrays was therefore performed on liver biopsies from patients with cirrhosis caused by either chronic alcohol consumption or chronic hepatitis C virus (HCV). RESULTS: Global gene expression patterns varied significantly depending upon etiology of liver disease, with a greater number of differentially regulated genes seen in HCV-infected patients. Many of the gene expression changes specifically observed in HCV-infected cirrhotic livers were expectedly associated with activation of the innate antiviral immune response. We also compared severity (CTP class) of cirrhosis for each etiology and identified gene expression patterns that differentiated ethanol-induced cirrhosis by class. CTP class A ethanol-cirrhotic livers showed unique expression patterns for genes implicated in the inflammatory response, including those related to macrophage activation and migration, as well as lipid metabolism and oxidative stress genes. CONCLUSION: Stages of liver cirrhosis could be differentiated based on gene expression patterns in ethanol-induced, but not HCV-induced, disease. In addition to genes specifically regulating the innate antiviral immune response, mechanisms responsible for differentiating chronic liver damage due to HCV or ethanol may be closely related to regulation of lipid metabolism and to effects of macrophage activation on deposition of extracellular matrix components. BioMed Central 2006-11-22 /pmc/articles/PMC1676004/ /pubmed/17121680 http://dx.doi.org/10.1186/1743-422X-3-98 Text en Copyright © 2006 Lederer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Lederer, Sharon L
Walters, Kathie-Anne
Proll, Sean
Paeper, Bryan
Robinzon, Shahar
Boix, Loreto
Fausto, Nelson
Bruix, Jordi
Katze, Michael G
Distinct cellular responses differentiating alcohol- and hepatitis C virus-induced liver cirrhosis
title Distinct cellular responses differentiating alcohol- and hepatitis C virus-induced liver cirrhosis
title_full Distinct cellular responses differentiating alcohol- and hepatitis C virus-induced liver cirrhosis
title_fullStr Distinct cellular responses differentiating alcohol- and hepatitis C virus-induced liver cirrhosis
title_full_unstemmed Distinct cellular responses differentiating alcohol- and hepatitis C virus-induced liver cirrhosis
title_short Distinct cellular responses differentiating alcohol- and hepatitis C virus-induced liver cirrhosis
title_sort distinct cellular responses differentiating alcohol- and hepatitis c virus-induced liver cirrhosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1676004/
https://www.ncbi.nlm.nih.gov/pubmed/17121680
http://dx.doi.org/10.1186/1743-422X-3-98
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