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

被引:13
作者
Yang, Po-Yu [1 ,2 ]
Ho, Dennis Chun-Yu [3 ,4 ]
Chen, Szu-Han [1 ]
Hsieh, Pei-Ling [5 ]
Liao, Yi-Wen [6 ]
Tsai, Lo-Lin [3 ,4 ]
Yu, Cheng-Chia [1 ,2 ,7 ,8 ]
Fang, Chih-Yuan [3 ,4 ,9 ]
机构
[1] Chung Shan Med Univ, Sch Dent, Taichung, Taiwan
[2] Chung Shan Med Univ Hosp, Dept Dent, Taichung, Taiwan
[3] Taipei Med Univ, Coll Oral Med, Sch Dent, Taipei, Taiwan
[4] Wan Fang Hosp, Dept Dent, Div Oral & Maxillofacial Surg, Taipei, Taiwan
[5] China Med Univ, Sch Med, Dept Anat, Taichung, Taiwan
[6] Chung Shan Med Univ Hosp, Dept Med Res, Taichung, Taiwan
[7] Chung Shan Med Univ, Inst Oral Sci, Taichung, Taiwan
[8] Chung Shan Med Univ, Inst Oral Sci, 110, Sec1, Jianguo N Rd, Taichung 40201, Taiwan
[9] Taipei Med Univ, Coll Oral Med, Sch Dent, 250, Wuxing St, Taipei 11031, Taiwan
关键词
Oral submucous fibrosis; MicroRNA-29c; Tropomyosin-1; Myofibroblast; EPITHELIAL-MESENCHYMAL TRANSITION; TGF-BETA REGULATION; RENAL FIBROSIS; MYOFIBROBLAST; INDUCTION; RENEWAL;
D O I
10.1016/j.jfma.2021.10.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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/).
引用
收藏
页码:1117 / 1122
页数:6
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