lncRNA NR2F2-AS1 inhibits the methylation of miR-494 to regulate oral squamous cell carcinoma cell proliferation

被引:3
|
作者
Liang, Yilei [1 ]
Wu, Xun [7 ]
Lee, Jinli [3 ]
Yu, Dahai [4 ]
Su, Jiping [5 ]
Guo, Mengzhu [4 ]
Meng, Ning [2 ]
Qin, Jiangyuan [6 ]
Fan, Xuemin [2 ]
机构
[1] Guangxi Med Univ, Dept Stomatol, Wuming Hosp, Nanning 530199, Guangxi, Peoples R China
[2] Guangxi Med Univ, Dept Maxillofacial Surg, Coll Stomatol, 10 Shuangyong Rd, Nanning 530199, Guangxi, Peoples R China
[3] 923 Hosp Joint Logist Support Force Chinese Peopl, Dept Gastroenterol, Nanning 530021, Guangxi, Peoples R China
[4] Guangxi Med Univ, Dept Stomatol, Affiliated Hosp 1, Nanning 530021, Guangxi, Peoples R China
[5] Guangxi Med Univ, ENT & HN Surg Dept, Affiliated Hosp 1, Nanning 530199, Guangxi, Peoples R China
[6] Guangxi Gen Hosp Chinese Peoples Armed Police For, Dept Otolaryngol, Nanning 530007, Guangxi, Peoples R China
[7] Southern Med Univ, Dept Maxillofacial Surg, Shenzhen Stomatol Hosp Pingshan, Shenzhen 518118, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Oral squamous cell carcinoma; NR2F2-AS1; MiR-494; Methylation;
D O I
10.1016/j.archoralbio.2021.105316
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: This study aimed to investigate the role of lncRNA NR2F2-AS1 in oral squamous cell carcinoma cells (OSCC). Materials and methods: The TCGA datasets were used to explore the differential expression of NR2F2-AS1 in OSCC. To further explore the potential interaction between NR2F2-AS1 and miR-494, SCC090 cells were transfected with the NR2F2-AS1 expression vector, NR2F2-AS1 siRNA, and a miR-494 mimic. The effect of NR2F2-AS1 on miR-494 methylation was evaluated by performing methylation-specific PCR (MSP). Cell Counting Kit-8 (CCK-8) assay was used to assess the effects of NR2F2-AS1 silencing and miR-494 and NR2F2-AS1 overexpression on OSCC cell proliferation. Results: NR2F2-AS1 expression was downregulated in OSCC and positively correlated with miR-494 expression. In OSCC cells, NR2F2-AS1 overexpression upregulated miR-494 level, while NR2F2-AS1 silencing decreased miR-494 expression. MSP results showed that NR2F2-AS1 overexpression decreased miR-494 methylation while NR2F2-AS1 silencing increased miR-494 methylation. In addition, NR2F2-AS1 silencing increased OSCC cell proliferation rate while overexpression of miR-494 and NR2F2-AS1 decreased OSCC cell proliferation. Furthermore, miR-494 overexpression attenuated the effects of NR2F2-AS1 silencing on cell proliferation. Conclusion: NR2F2-AS1 may inhibit miR-494 methylation to regulate cell proliferation in OSCC. Conclusion: NR2F2-AS1 may inhibit miR-494 methylation to regulate cell proliferation in OSCC. Availability of data and materials: The analyzed data sets generated during the study are available from the corresponding author upon reasonable request.
引用
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页数:6
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