Proteomics and liver fibrosis: identifying markers of fibrogenesis

被引:12
|
作者
Mas, Valeria R. [1 ]
Fisher, Robert A. [1 ]
Archer, Kellie J. [1 ]
Maluf, Daniel G. [1 ]
机构
[1] Virginia Commonwealth Univ, Transplant Mol Lab, Transplant Div, Dept Surg, Richmond, VA 23298 USA
关键词
biomarkers; cirrhosis; hepatitis B virus; hepatitis C virus; liver fibrosis; proteomics; HEPATITIS-C-VIRUS; HEPATOCELLULAR-CARCINOMA; TRANSIENT ELASTOGRAPHY; NONINVASIVE MARKERS; GEL-ELECTROPHORESIS; GENE-EXPRESSION; SYSTEMS BIOLOGY; CIRRHOSIS; SERUM; BIOMARKERS;
D O I
10.1586/EPR.09.59
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Chronic hepatic disease damages the liver and the resulting wound-healing process might lead to liver fibrosis and subsequent cirrhosis development. Fibrosis is the excessive deposition of extracellular matrix (ECM) in the tissue as consequence of chronic liver damage. The fibrotic response triggers almost all of the complications of end-stage liver disease, including portal hypertension, ascites, encephalopathy, synthetic dysfunction and impaired metabolic capacity. Thus, efforts to understand and attenuate fibrosis have direct clinical implications. Reliable, accurate, disease-specific, noninvasive biomarkers of fibrosis and fibrogenesis in order to prevent or minimize the impact of the chronic liver disease progression are a critical need. This review aims to provide an overview of the possibilities that proteome technology can offer to the knowledge, diagnosis and prognosis of liver fibrosis.
引用
收藏
页码:421 / 431
页数:11
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