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TLRs, Alcohol, HCV, and Tumorigenesis

Chronic liver damage caused by viral infection, alcohol, or obesity can result in increased risk for hepatocellular carcinoma (HCC). Ample epidemiological evidence suggests that there is a strong synergism between hepatitis C virus (HCV) and alcoholic liver diseases (ALD). The Toll-like receptor (TL...

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Autor principal: Machida, Keigo
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038599/
https://www.ncbi.nlm.nih.gov/pubmed/21331379
http://dx.doi.org/10.1155/2010/518674
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author Machida, Keigo
author_facet Machida, Keigo
author_sort Machida, Keigo
collection PubMed
description Chronic liver damage caused by viral infection, alcohol, or obesity can result in increased risk for hepatocellular carcinoma (HCC). Ample epidemiological evidence suggests that there is a strong synergism between hepatitis C virus (HCV) and alcoholic liver diseases (ALD). The Toll-like receptor (TLR) signaling pathway is upregulated in chronic liver diseases. Alcoholism is associated with endotoxemia that stimulates expression of proinflammatory cytokine expression and inflammation in the liver and fat tissues. Recent studies of HCC have centered on cancer-initiating stem cell (CSC), including detection of CSC in cancer, identification of CSC markers, and isolation of CSC from human HCC cell lines. Synergism between alcohol and HCV may lead to liver tumorigenesis through TLR signaling.
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spelling pubmed-30385992011-02-17 TLRs, Alcohol, HCV, and Tumorigenesis Machida, Keigo Gastroenterol Res Pract Review Article Chronic liver damage caused by viral infection, alcohol, or obesity can result in increased risk for hepatocellular carcinoma (HCC). Ample epidemiological evidence suggests that there is a strong synergism between hepatitis C virus (HCV) and alcoholic liver diseases (ALD). The Toll-like receptor (TLR) signaling pathway is upregulated in chronic liver diseases. Alcoholism is associated with endotoxemia that stimulates expression of proinflammatory cytokine expression and inflammation in the liver and fat tissues. Recent studies of HCC have centered on cancer-initiating stem cell (CSC), including detection of CSC in cancer, identification of CSC markers, and isolation of CSC from human HCC cell lines. Synergism between alcohol and HCV may lead to liver tumorigenesis through TLR signaling. Hindawi Publishing Corporation 2010 2011-02-09 /pmc/articles/PMC3038599/ /pubmed/21331379 http://dx.doi.org/10.1155/2010/518674 Text en Copyright © 2010 Keigo Machida. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Machida, Keigo
TLRs, Alcohol, HCV, and Tumorigenesis
title TLRs, Alcohol, HCV, and Tumorigenesis
title_full TLRs, Alcohol, HCV, and Tumorigenesis
title_fullStr TLRs, Alcohol, HCV, and Tumorigenesis
title_full_unstemmed TLRs, Alcohol, HCV, and Tumorigenesis
title_short TLRs, Alcohol, HCV, and Tumorigenesis
title_sort tlrs, alcohol, hcv, and tumorigenesis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038599/
https://www.ncbi.nlm.nih.gov/pubmed/21331379
http://dx.doi.org/10.1155/2010/518674
work_keys_str_mv AT machidakeigo tlrsalcoholhcvandtumorigenesis