Inhibition of lncRNA HOTTIP ameliorated myofibroblast activities and inflammatory cytokines in oral submucous fibrosis

被引:16
作者
Lee, Yu-Hsien [1 ,2 ]
Yu, Cheng-Chia [1 ,2 ,3 ]
Hsieh, Pei-Ling [4 ]
Liao, Yi-Wen [3 ,5 ]
Yu, Chuan-Hang [1 ,2 ]
Su, Tzu-Rong [6 ,7 ]
机构
[1] Chung Shan Med Univ, Sch Dent, 110,Sec 1,Jianguo N Rd, Taichung 40201, Taiwan
[2] Chung Shan Med Univ Hosp, Dept Dent, Taichung, Taiwan
[3] Chung Shan Med Univ, Inst Oral Sci, Taichung, Taiwan
[4] China Med Univ, Sch Med, Dept Anat, Taichung, Taiwan
[5] Chung Shan Med Univ Hosp, Dept Med Res, Taichung, Taiwan
[6] Antai Med Care Cooperat Antai Tian Sheng Mem Hosp, Dept Dent, Pingtung, Taiwan
[7] Meiho Univ, Dept Beauty Sci, Pingtung, Taiwan
关键词
HOTTIP; Myofibroblast; Oral submucous fibrosis; NECROSIS-FACTOR-ALPHA; FIBROBLASTS; RISK;
D O I
10.1016/j.jfma.2020.11.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Purpose: Long non-coding RNA HOXA transcript at the distal tip (HOTTIP) has been reported to contribute to multiple carcinomas, but whether it involves in the progression of precancerous conditions remains to be determined. Oral submucous fibrosis (OSF) has been known as an oral potentially malignant disorder and attributed to the persistent activation of the myofibroblast. Methods: The relative expression of HOTTIP in OSF tissues has been employed by RNA sequencing and RT-PCR analysis. HOTTIP associated myofibroblasts activities and markers in fibrotic buccal mucosal fibroblast (fBMFs) through loss of function approaches have been evaluated. Results: In the present study, we found that the expression of HOTTIP was overexpressed in the OSF tissues and positively correlated with several fibrosis markers. To investigate its significance of myofibroblast activation, we first verified the expression level of HOTTIP in the patient-derived fibrotic buccal mucosal fibroblast (fBMFs) was upregulated and conducted the shRNA-mediated knockdown experiment to inhibit its expression followed by numerous examinations. We demonstrated that suppression of HOTTIP downregulated the expression of myofibroblast marker, alpha-SMA, and type I collagen along with the diminished myofibroblast activities (collagen gel contraction and migration capacities). Furthermore, we showed that silencing HOTTIP lessened the production of various pro-inflammatory cytokines (IL-6 and TNF-alpha). Conclusion: Collectively, our results suggest that HOTTIP plays a crucial role in the persistent activation of myofibroblasts as well as the chronic inflammation and collagen deposition. Copyright (C) 2021, Formosan Medical Association. Published by Elsevier Taiwan LLC.
引用
收藏
页码:1188 / 1193
页数:6
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