Long non-coding RNA-H19 antagonism protects against renal fibrosis

被引:79
作者
Xie, Hong [1 ]
Xue, Jing-Dong [1 ]
Chao, Feng [1 ]
Jin, Yan-Feng [1 ]
Fu, Qiang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Peoples Hosp 6, Dept Urol, Shanghai, Peoples R China
关键词
long non-coding RNA; renal fibrosis; microRNA; unilateral ureteral obstruction; TGF-BETA; MOLECULAR-MECHANISMS; PULMONARY-FIBROSIS; CANCER METASTASIS; KIDNEY; MICRORNAS; DISEASE; RNAS; TARGET; GROWTH;
D O I
10.18632/oncotarget.10444
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although long non-coding RNAs (lncRNAs) are important players in the initiation and progression of many pathological processes, the role of lncRNAs in renal fibrosis still remains unclear. We showed that lncRNA-H19 expression was significantly upregulated in TGF-beta 2-induced HK-2 cell fibrosis and unilateral ureteral obstruction (UUO)-induced renal fibrosis in vivo. H19 knockdown significantly attenuated renal fibrosis in vitro and in vivo. LncRNA-H19, miR-17, and fibronectin constituted to a regulatory network involved in renal fibrosis. We also detected up-regulated H19 expression and down-regulated miR-17 expression in the early and advanced animal models of renal fibrosis. This study indicates that H19 up-regulation contributes to renal fibrosis. H19 inhibition might represent a novel anti-fibrotic treatment in renal diseases.
引用
收藏
页码:51473 / 51481
页数:9
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