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Signal Transducer and Activator of Transcription 3 in Liver Diseases: A Novel Therapeutic Target
Signal transducer and activator of transcription 3 (STAT3) is a transcription factor that is activated by many cytokines and growth factors and plays a key role in cell survival, proliferation, and differentiation. STAT3 activation is detected virtually in all rodent models of liver injury and in hu...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Ivyspring International Publisher
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3088876/ https://www.ncbi.nlm.nih.gov/pubmed/21552420 |
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author | Wang, Hua Lafdil, Fouad Kong, Xiaoni Gao, Bin |
author_facet | Wang, Hua Lafdil, Fouad Kong, Xiaoni Gao, Bin |
author_sort | Wang, Hua |
collection | PubMed |
description | Signal transducer and activator of transcription 3 (STAT3) is a transcription factor that is activated by many cytokines and growth factors and plays a key role in cell survival, proliferation, and differentiation. STAT3 activation is detected virtually in all rodent models of liver injury and in human liver diseases. In this review, we highlight recent advances of STAT3 signaling in liver injury, steatosis, inflammation, regeneration, fibrosis, and hepatocarcinogenesis. The cytokines and small molecules that activate STAT3 in hepatocytes may have therapeutic benefits to treat acute liver injury, fatty liver disease, and alcoholic hepatitis, while blockage of STAT3 may have a therapeutic potential to prevent and treat liver cancer. |
format | Text |
id | pubmed-3088876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-30888762011-05-06 Signal Transducer and Activator of Transcription 3 in Liver Diseases: A Novel Therapeutic Target Wang, Hua Lafdil, Fouad Kong, Xiaoni Gao, Bin Int J Biol Sci Review Signal transducer and activator of transcription 3 (STAT3) is a transcription factor that is activated by many cytokines and growth factors and plays a key role in cell survival, proliferation, and differentiation. STAT3 activation is detected virtually in all rodent models of liver injury and in human liver diseases. In this review, we highlight recent advances of STAT3 signaling in liver injury, steatosis, inflammation, regeneration, fibrosis, and hepatocarcinogenesis. The cytokines and small molecules that activate STAT3 in hepatocytes may have therapeutic benefits to treat acute liver injury, fatty liver disease, and alcoholic hepatitis, while blockage of STAT3 may have a therapeutic potential to prevent and treat liver cancer. Ivyspring International Publisher 2011-04-27 /pmc/articles/PMC3088876/ /pubmed/21552420 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. |
spellingShingle | Review Wang, Hua Lafdil, Fouad Kong, Xiaoni Gao, Bin Signal Transducer and Activator of Transcription 3 in Liver Diseases: A Novel Therapeutic Target |
title | Signal Transducer and Activator of Transcription 3 in Liver Diseases: A Novel Therapeutic Target |
title_full | Signal Transducer and Activator of Transcription 3 in Liver Diseases: A Novel Therapeutic Target |
title_fullStr | Signal Transducer and Activator of Transcription 3 in Liver Diseases: A Novel Therapeutic Target |
title_full_unstemmed | Signal Transducer and Activator of Transcription 3 in Liver Diseases: A Novel Therapeutic Target |
title_short | Signal Transducer and Activator of Transcription 3 in Liver Diseases: A Novel Therapeutic Target |
title_sort | signal transducer and activator of transcription 3 in liver diseases: a novel therapeutic target |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3088876/ https://www.ncbi.nlm.nih.gov/pubmed/21552420 |
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