Wnt/β-Catenin Signaling as a Potential Target for the Treatment of Liver Cirrhosis Using Antifibrotic Drugs

被引:108
作者
Nishikawa, Koji [1 ,2 ]
Osawa, Yosuke [3 ]
Kimura, Kiminori [1 ,2 ]
机构
[1] Tokyo Metropolitan Canc, Dept Hepatol, Bunkyo Ku, 3-18-22 Honkomagome, Tokyo 1138677, Japan
[2] Komagome Hosp, Ctr Infect Dis, Bunkyo Ku, 3-18-22 Honkomagome, Tokyo 1138677, Japan
[3] Natl Ctr Global Hlth & Med, Res Ctr Hepatitis & Immunol, 1-7-1 Kohnodai, Ichikawa, Chiba 2728516, Japan
关键词
liver fibrosis; Wnt; -catenin; PRI-724; BETA-CATENIN; TISSUE-REPAIR; STEM-CELLS; WNT; FIBROSIS; INJURY; ROLES; INHIBITION; EXPRESSION; DISEASE;
D O I
10.3390/ijms19103103
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cirrhosis is a form of liver fibrosis resulting from chronic hepatitis and caused by various liver diseases, including viral hepatitis, alcoholic liver damage, nonalcoholic steatohepatitis, and autoimmune liver disease. Cirrhosis leads to various complications, resulting in poor prognoses; therefore, it is important to develop novel antifibrotic therapies to counter liver cirrhosis. Wnt/-catenin signaling is associated with the development of tissue fibrosis, making it a major therapeutic target for treating liver fibrosis. In this review, we present recent insights into the correlation between Wnt/-catenin signaling and liver fibrosis and discuss the antifibrotic effects of the cAMP-response element binding protein/-catenin inhibitor PRI-724.
引用
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页数:12
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