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

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 cel...

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Detalles Bibliográficos
Autores principales: Zhang, Ye, Guo, Bingyu, Hui, Qiang, Li, Wei, Chang, Peng, Tao, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072149/
https://www.ncbi.nlm.nih.gov/pubmed/29845237
http://dx.doi.org/10.3892/mmr.2018.9099
Descripción
Sumario: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.