Downregulation of miR-637 promotes proliferation and metastasis by targeting Smad3 in keloids

被引:24
作者
Zhang, Ye [1 ]
Guo, Bingyu [1 ]
Hui, Qiang [1 ]
Li, Wei [1 ]
Chang, Peng [1 ]
Tao, Kai [1 ]
机构
[1] Gen Hosp Shenyang Mil Reg, Dept Reconstruct & Plast Surg, 83 Wenhua Rd, Shenyang 110016, Liaoning, Peoples R China
关键词
smad3; keloid; miR-637; proliferation; metastasis; SIGNALING PATHWAY; FIBROBLASTS; EXPRESSION; GROWTH; CELLS; INHIBITION; ACTIVATION; APOPTOSIS; INVASION; MARKER;
D O I
10.3892/mmr.2018.9099
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Keloids are a type of abnormal scar tissue. MicroRNAs (miRNAs) exhibit a pivotal role in the regulation of cell proliferation and metastasis of keloids. miRNA microarray revealed that miR-637 was one of the most frequently altered miRNAs in keloids. Furthermore, upregulation of miR-637 inhibited cell proliferation and metastasis by targeting mothers against decapentaplegic homolog (Smad)3, one of the important proteins that affects the formation of keloids. Further studies demonstrated that miR-637 regulated the proliferation and metastasis of human keloid fibroblast (HKF) cells by mediating the Smad3 signaling pathway. Overall, the present findings suggest that miR-637 may be a promising therapeutic target in keloids.
引用
收藏
页码:1628 / 1636
页数:9
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