Literature DB >> 16420505

Therapeutic strategies against TGF-beta signaling pathway in hepatic fibrosis.

Xingjun Liu1, Han Hu, James Q Yin.   

Abstract

Hepatic fibrosis is the common wound-healing response to chronic liver injury. In this process, activation of hepatic stellate cells is characteristic of cell proliferation and migration, production of collagen and other extracellular matrix (ECM) molecules, and contraction after transforming into myofibroblasts. It has been shown that the fibrogenic process is prominently regulated by transforming growth factor-beta1 (TGF-beta1) and that the specific blockade of TGF-beta1/Smad3 signaling may therapeutically intervene the fibrosis of various tissues. In this review, we attempt to integrate recent advances in the understanding of the mechanisms underlying TGF-beta1/Smad3 pathway modulation of ECM gene expression in the context of liver fibrosis, discuss intervention strategies targeting the blockade of related signal pathways, and look into novel ways to the safe and efficacious prevention and treatment of hepatic fibrosis.

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Year:  2006        PMID: 16420505     DOI: 10.1111/j.1478-3231.2005.01192.x

Source DB:  PubMed          Journal:  Liver Int        ISSN: 1478-3223            Impact factor:   5.828


  89 in total

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10.  Inhibition of IRF3 expression reduces TGF-β1-induced proliferation of hepatic stellate cells.

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Journal:  J Physiol Biochem       Date:  2015-11-26       Impact factor: 4.158

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