肺纤维化
矽肺
非规范的
医学
转化生长因子
信号转导
纤维化
药理学
病理
化学
内科学
生物
生物化学
细胞生物学
作者
Tong-Tong Liu,Hai-Fei Sun,Ming-Ze Tang,Hao-Ran Shen,Zhen Shen,Yanxing Han,Yun Zhan,Jian‐Dong Jiang
标识
DOI:10.1186/s12967-024-05399-x
摘要
The collective data suggest that BIC prevents both FMT and EMT processes, in turn, reducing aberrant collagen deposition. Our findings demonstrate for the first time that BIC ameliorates inflammatory cytokine secretion, in particular, TGF-β1, and consequently inhibits FMT and EMT via TGF-β1 canonical and non-canonical pathways, ultimately resulting in reduction of aberrant collagen deposition and slower progression of silicosis, supporting its potential as a novel therapeutic agent.
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