| Literature DB >> 29138094 |
Zhenlong Xin1, Zhiqiang Ma2, Wei Hu3, Shuai Jiang4, Zhi Yang3, Tian Li3, Fulin Chen5, Guozhan Jia6, Yang Yang7.
Abstract
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.Entities:
Keywords: Aging; Extracellular matrix; FOXO1/3; Fibroblast; Fibrosis
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Year: 2017 PMID: 29138094 DOI: 10.1016/j.arr.2017.11.002
Source DB: PubMed Journal: Ageing Res Rev ISSN: 1568-1637 Impact factor: 10.895