Suppr超能文献

长链非编码 RNA NR2F2-AS1 通过抑制 miR-494 的甲基化调节口腔鳞状细胞癌细胞的增殖。

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

机构信息

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.

出版信息

Arch Oral Biol. 2022 Feb;134:105316. doi: 10.1016/j.archoralbio.2021.105316. Epub 2021 Nov 19.

Abstract

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.

AVAILABILITY OF DATA AND MATERIALS

The analyzed data sets generated during the study are available from the corresponding author upon reasonable request.

摘要

目的

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。

材料和方法

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。

结果

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。

结论

NR2F2-AS1 可能通过抑制 miR-494 甲基化来调节 OSCC 中的细胞增殖。

数据和材料的可利用性

研究中生成的分析数据集可应合理要求向通讯作者索取。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验