Antagonism of Transforming Growth Factor-Β Signaling Inhibits Fibrosis-Related Genes

被引:0
|
作者
Xing-Jun Liu
Cheng-Mai Ruan
Xian-Feng Gong
Xing-Zhou Li
Huai-Liang Wang
Min-Wei Wang
James Q. Yin
机构
[1] Institute of Biophysics,Protein & Peptide Pharmaceutical Laboratory
[2] Chinese Academy of Sciences,School of Pharmacy
[3] Shengyang Pharmaceutical University,Institute of Pharmacology Toxicology
[4] The Academy of Military Medical Sciences,School of Basic Medicine
[5] China Medical University,undefined
来源
Biotechnology Letters | 2005年 / 27卷
关键词
fibrosis; siRNA; Smad3 protein; transforming growth factor-β1;
D O I
暂无
中图分类号
学科分类号
摘要
In the fibrotic process, the transforming growth factor-β1 (TGF-β1)/Smad3 (Sma- and Mad-related protein␣3) signaling plays a central role. To screen for antagonists of TGF-β1/Smad3 signaling and to investigate their effects on the genes related to fibrosis, we construct a molecular model with a luciferase reporter gene. Results showed that both SB-431542 [4-(5-benzo[1,3]dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)-benzamide] and small interference RNA (siRNA) against Smad3 could dose-dependently suppress the reporter gene. More importantly, they both significantly inhibited the expression of plasminogen activator inhibitor-type 1 (PAI-1) and type I collagenα1 (Col Iα1) genes in rat hepatic stellate cells. Thus, SB-431542 and Smad3/siRNA may be potential therapeutics for fibrosis.
引用
收藏
页码:1609 / 1615
页数:6
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