Department of Stomatology, Wuming Hospital of Guangxi Medical University, Nanning City, Guangxi Province 530199, China.
Department of Maxillofacial Surgery, Southern Medical University Shenzhen Stomatology Hospital (Pingshan), Shenzhen City, Guangdong Province, 518118, China.
Arch Oral Biol. 2022 Feb;134:105316. doi: 10.1016/j.archoralbio.2021.105316. Epub 2021 Nov 19.
This study aimed to investigate the role of lncRNA NR2F2-AS1 in oral squamous cell carcinoma cells (OSCC).
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.
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.
NR2F2-AS1 may inhibit miR-494 methylation to regulate cell proliferation in OSCC.
The analyzed data sets generated during the study are available from the corresponding author upon reasonable request.
本研究旨在探讨长链非编码 RNA NR2F2-AS1 在口腔鳞状细胞癌细胞(OSCC)中的作用。
使用 TCGA 数据集探讨 NR2F2-AS1 在 OSCC 中的差异表达。为了进一步探讨 NR2F2-AS1 与 miR-494 之间的潜在相互作用,将 NR2F2-AS1 表达载体、NR2F2-AS1 siRNA 和 miR-494 模拟物转染至 SCC090 细胞。通过甲基化特异性 PCR(MSP)评估 NR2F2-AS1 对 miR-494 甲基化的影响。通过细胞计数试剂盒-8(CCK-8)测定评估 NR2F2-AS1 沉默和 miR-494 及 NR2F2-AS1 过表达对 OSCC 细胞增殖的影响。
NR2F2-AS1 在 OSCC 中表达下调,与 miR-494 表达呈正相关。在 OSCC 细胞中,过表达 NR2F2-AS1 上调 miR-494 水平,而沉默 NR2F2-AS1 则降低 miR-494 表达。MSP 结果表明,NR2F2-AS1 过表达降低 miR-494 甲基化,而 NR2F2-AS1 沉默增加 miR-494 甲基化。此外,NR2F2-AS1 沉默增加 OSCC 细胞增殖率,而过表达 miR-494 和 NR2F2-AS1 则降低 OSCC 细胞增殖率。此外,miR-494 过表达减弱了 NR2F2-AS1 沉默对细胞增殖的影响。
NR2F2-AS1 可能通过抑制 miR-494 甲基化来调节 OSCC 中的细胞增殖。
研究中生成的分析数据集可应合理要求向通讯作者索取。