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miR-1246 as a therapeutic target in oral submucosa fibrosis pathogenesis

Authors :
Chuan-Hang Yu
Ming-Yung Chou
Pei-Ling Hsieh
Chia-Ming Liu
Pin Ju Chueh
Po-Yu Yang
Taichen Lin
Yi-Wen Liao
Cheng-Chia Yu
Source :
Journal of the Formosan Medical Association, Vol 118, Iss 7, Pp 1093-1098 (2019)
Publication Year :
2019
Publisher :
Elsevier, 2019.

Abstract

Background/purpose: Oral submucous fibrosis (OSF) is a precancerous condition of oral cancer with a complex etiology. Our previous work has demonstrated that non-coding RNA miR-1246 contributes to the cancer stemness of oral cancer. In the current study, we sought to investigate the effect of the inhibition of miR-1246 on the oral fibrogenesis. Methods: The expression levels of miR-1246 in OSF tissues and fibrotic buccal mucosal fibroblasts (fBMFs) were examined by qRT-PCR. Collagen gel contraction and migration assays were conducted to evaluate the myofibroblast activities. The relationship between miR-1246 and type I collagen was assessed and the protein expression of type I collagen was determined by Western blot. Results: MiR-1246 expression was upregulated in both OSF specimen and fBMFs compared to the normal counterparts. Inhibition of miR-1246 successfully suppressed the myofibroblast activities, including collagen gel contractility and migration capacity. Moreover, the expression of miR-1246 was positively correlated with type I collagen and the expression of type I collagen was abrogated by repression of miR-1246. Conclusion: MiR-1246 is not only critical to the maintenance of oral stemness but also important to the activation of myofibroblasts. Our results showed that miR-1246 is positively associated with the type I collagen, which may be a downstream effector of miR-1246 and responsible for the fibrosis effect on fBMFs. Keywords: Oral submucous fibrosis, MicroRNA-1246, Type I collagen, Buccal mucosal fibroblasts

Details

Language :
English
ISSN :
09296646
Volume :
118
Issue :
7
Database :
OpenAIRE
Journal :
Journal of the Formosan Medical Association
Accession number :
edsair.doi.dedup.....6391b433f7e76a8abae57c4eef5ac562