4.3 Article

Original Article Down-regulation of miR-29c promotes the progression of oral submucous fibrosis through targeting tropomyosin-1

Journal

JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
Volume 121, Issue 6, Pages 1117-1122

Publisher

ELSEVIER TAIWAN
DOI: 10.1016/j.jfma.2021.10.006

Keywords

Oral submucous fibrosis; MicroRNA-29c; Tropomyosin-1; Myofibroblast

Funding

  1. Chung Shan Med-ical University Hospital [CSH-2019-C-035]
  2. Wan Fang Hospital [109-wf-eva-10]

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This study found that miR-29c expression is downregulated in oral submucous fibrosis (OSF). Transfection of miR-29c mimic reduced the migration ability and collagen gel contractility of fibrotic buccal mucosal fibroblasts (fBMFs), while inhibition of miR-29c induced myofibroblast phenotypes in normal BMFs. TPM1 was identified as a direct target of miR-29c, and its expression was suppressed in fBMFs transfected with miR-29c mimic. These findings suggest that upregulation of miR-29c may ameliorate the progression of OSF.
Background/Purpose: Various microRNAs (miRs) have been found to be associated with the development of the precancerous condition of the oral cavity, oral submucous fibrosis (OSF). The expression of miR-29c is dysregulated in oral cancer, but its role in OSF has not been investigated. The purpose of the study is to investigate the functional role of miR-29c and its target in OSF.Methods: The expression levels of miR-29c in OSF tissues and fibrotic buccal mucosal fibroblasts (fBMFs) were assessed using next-generation sequencing and real-time Polymerase Chain Reaction (PCR) analysis. MiR-29c mimic and inhibitors were employed to examine its functional role of myofibroblast transdifferentiation. In addition, several myofibroblast phenotypes, such as collagen gel contraction and migration were tested, and a luciferase reporter assay was conducted to confirm the relationship between miR-29c and its predicted target, tropomyosin-1 (TPM1).Results: We observed that miR-29c expression was downregulated in fBMFs. fBMFs transfected with miR-29c mimics exhibited reduced migration ability and collagen gel contractility, whereas inhibition of miR-29c in normal BMFs induced the myofibroblast phenotypes. Results from the luciferase reporter assay showed that TPM1 was a direct target of miR-29c and the expression of TPM1 was suppressed in the fBMFs transfected with miR-29c mimics. Besides, we confirmed that the expression of miR-29c was indeed downregulated in OSF specimens.Conclusion: MiR-29c seems to exert an inhibitory effect on myofibroblast activation, such as collagen gel contractility and migration ability, via suppressing TPM1. These results suggested that approaches to upregulate miR-29c may be able to ameliorate the progression of OSF. Copyright 2021, Formosan Medical Association. Published by Elsevier Taiwan LLC. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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