福克斯O1
细胞外基质
癌症研究
医学
肾脏疾病
生物
蛋白激酶B
纤维化
细胞生物学
信号转导
病理
内科学
作者
Zhenlong Xin,Zhiqiang Ma,Wei Hu,Shuai Jiang,Zhi Yang,Tian Li,Fulin Chen,Guo‐Zhan Jia,Yang Yang
标识
DOI:10.1016/j.arr.2017.11.002
摘要
Fibrosis is a universally age-related disease that involves nearly all organs. It is typically initiated by organic injury and eventually results in organ failure. There are still few effective therapeutic strategy targets for fibrogenesis. Forkhead box proteins O1 and O3 (FOXO1/3) have been shown to have favorable inhibitory effects on fibroblast activation and subsequent extracellular matrix production and can ameliorate fibrosis levels in numerous organs, including the heart, liver, lung, and kidney; they are therefore promising targets for anti-fibrosis therapy. Moreover, we can develop appropriate strategies to make the best use of FOXO1/3's anti-fibrosis properties. The information reviewed here should be significant for understanding the roles of FOXO1/3 in fibrosis and should contribute to the design of further studies related to FOXO1/3 and the fibrotic response and shed light on a potential treatment for fibrosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI