共 23 条
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/).
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页码:1117 / 1122
页数:6
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