| Literature DB >> 26206573 |
Yukinori Koyama1, David A Brenner2.
Abstract
Liver fibrosis is an outcome of many chronic diseases, and often results in cirrhosis, liver failure, and portal hypertension. Liver transplantation is the only treatment available for patients with advanced stages of liver cirrhosis. Therefore, alternative methods are required to develop new strategies for anti-fibrotic therapy. Various kinds of hepatocyte injuries cause inflammatory reactions, which lead to activation of hepatic stellate cells (HSCs). Continuous liver injuries maintain these activated HSCs, and they are called as myofibroblasts. Myofibroblasts proliferate in response to various kinds of cytokines and produce extracellular matrix proteins (ECMs). Myofibroblasts undergo apoptosis and inactivation when the underlying causative etiologies are cleared. Here, we describe the current knowledge of targeting the activated HSCs as a therapeutic target for liver fibrosis.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26206573 PMCID: PMC4734896 DOI: 10.1016/j.clinre.2015.06.011
Source DB: PubMed Journal: Clin Res Hepatol Gastroenterol ISSN: 2210-7401 Impact factor: 2.947