New Developments on the Treatment of Liver Fibrosis

被引:103
作者
Koyama, Yukinori [1 ]
Xu, Jun [1 ]
Liu, Xiao [1 ]
Brenner, David A. [1 ]
机构
[1] Univ Calif San Diego, Sch Med, 9500 Gilman Dr, San Diego, CA 92093 USA
关键词
Liver fibrosis; Hepatocytes; Hepatic stellate cells; Inflammation; Myofibroblasts; HEPATIC STELLATE CELLS; GROWTH-FACTOR-BETA; SERUM AMYLOID P; ANTIBODY FRESOLIMUMAB; LYSOPHOSPHATIDIC ACID; TISSUE INHIBITOR; METALLOPROTEINASE-1; ENDOCANNABINOIDS; DIFFERENTIATION; PROLIFERATION;
D O I
10.1159/000445269
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Liver fibrosis results from many chronic injuries and often progresses to cirrhosis, liver failure, portal hypertension, and hepatocellular carcinoma. Liver transplantation is the only treatment available for patients with advanced stages of liver fibrosis. Therefore, new strategies for anti-fibrotic therapy are required. Various kinds of hepatocyte damage result in inflammation, which leads to the activation of hepatic stellate cells (HSCs), which are the major source of myofibroblasts in the liver. Myofibroblasts proliferate in response to various kinds of cytokines, chemokines, and growth factors and produce extracellular matrix proteins, which forms the fibrous scar. Myofibroblasts undergo apoptosis and inactivation when the underlying causative etiologies are cleared. Here we describe our current knowledge of targeting the steps in HSC activation as therapeutic target for liver fibrosis. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:589 / 596
页数:8
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