| Literature DB >> 28418584 |
Maho Ide1, Masatoshi Jinnin1, Yukiko Tomizawa1, Zhongzhi Wang1, Ikko Kajihara1, Satoshi Fukushima1, Yoshinobu Hashizume2, Yoshihide Asano3, Hironobu Ihn1.
Abstract
Inhibition of transforming growth factor (TGF)-β1 signalling may be one of the most reliable approaches to treat skin fibrosis of scleroderma. Although there have been many basic researches of TGF-β blockade reagents, few of them were proved to have inhibitory effects on fibrosis both in vitro and in vivo. In this study, we randomly chose four commercially available low molecular weight compounds (Repsox, LY2109761, LY364947 and K02288) from TGF-β1 inhibitor library, and compared their antifibrotic effects in vitro and in vivo. We demonstrated that Repsox has the most potent inhibitory effects on TGF-β-induced expression of CTGF and collagen of cultured normal dermal fibroblasts in vitro and their constitutive overexpression of scleroderma fibroblast in vitro. In addition, Repsox could attenuate skin fibrosis by bleomycin in vivo, via the downregulation of CTGF or collagen. Our results may facilitate clinical trial of Repsox against fibrotic diseases in future.Entities:
Keywords: fibrosis; scleroderma
Mesh:
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Year: 2017 PMID: 28418584 DOI: 10.1111/exd.13366
Source DB: PubMed Journal: Exp Dermatol ISSN: 0906-6705 Impact factor: 3.960