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Research progress on signaling pathways in cirrhotic portal hypertension

Portal hypertension (PHT) is an important consequence of liver cirrhosis, which can lead to complications that adversely affect a patient’s quality of life and survival, such as upper gastrointestinal bleeding, ascites, and portosystemic encephalopathy. In recent years, advances in molecular biology...

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Detalles Bibliográficos
Autores principales: Xu, Wen, Liu, Ping, Mu, Yong-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163134/
https://www.ncbi.nlm.nih.gov/pubmed/30283796
http://dx.doi.org/10.12998/wjcc.v6.i10.335
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author Xu, Wen
Liu, Ping
Mu, Yong-Ping
author_facet Xu, Wen
Liu, Ping
Mu, Yong-Ping
author_sort Xu, Wen
collection PubMed
description Portal hypertension (PHT) is an important consequence of liver cirrhosis, which can lead to complications that adversely affect a patient’s quality of life and survival, such as upper gastrointestinal bleeding, ascites, and portosystemic encephalopathy. In recent years, advances in molecular biology have led to major discoveries in the pathological processes of PHT, including the signaling pathways that may be involved: PI3K-AKT-mTOR, RhoA/Rho-kinase, JAK2/STAT3, and farnesoid X receptor. However, the pathogenesis of PHT is complex and there are numerous pathways involved. Therefore, the targeting of signaling pathways for medical management is lagging. This article summarizes the progress that has been made in understanding the signaling pathways in PHT, and provides ideas for treatment of the disorder.
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spelling pubmed-61631342018-10-03 Research progress on signaling pathways in cirrhotic portal hypertension Xu, Wen Liu, Ping Mu, Yong-Ping World J Clin Cases Minireviews Portal hypertension (PHT) is an important consequence of liver cirrhosis, which can lead to complications that adversely affect a patient’s quality of life and survival, such as upper gastrointestinal bleeding, ascites, and portosystemic encephalopathy. In recent years, advances in molecular biology have led to major discoveries in the pathological processes of PHT, including the signaling pathways that may be involved: PI3K-AKT-mTOR, RhoA/Rho-kinase, JAK2/STAT3, and farnesoid X receptor. However, the pathogenesis of PHT is complex and there are numerous pathways involved. Therefore, the targeting of signaling pathways for medical management is lagging. This article summarizes the progress that has been made in understanding the signaling pathways in PHT, and provides ideas for treatment of the disorder. Baishideng Publishing Group Inc 2018-09-26 2018-09-26 /pmc/articles/PMC6163134/ /pubmed/30283796 http://dx.doi.org/10.12998/wjcc.v6.i10.335 Text en ©The Author(s) 2018. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Minireviews
Xu, Wen
Liu, Ping
Mu, Yong-Ping
Research progress on signaling pathways in cirrhotic portal hypertension
title Research progress on signaling pathways in cirrhotic portal hypertension
title_full Research progress on signaling pathways in cirrhotic portal hypertension
title_fullStr Research progress on signaling pathways in cirrhotic portal hypertension
title_full_unstemmed Research progress on signaling pathways in cirrhotic portal hypertension
title_short Research progress on signaling pathways in cirrhotic portal hypertension
title_sort research progress on signaling pathways in cirrhotic portal hypertension
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163134/
https://www.ncbi.nlm.nih.gov/pubmed/30283796
http://dx.doi.org/10.12998/wjcc.v6.i10.335
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