Department of Stomatology, The Second Affiliated Hospital of Mudanjiang Medical University, Mudanjiang, China.
Eye 3 Division of Red Flag Hospital of Mudanjiang Medical University, Mudanjiang, China.
J Oral Pathol Med. 2020 Apr;49(4):286-293. doi: 10.1111/jop.13015. Epub 2020 Mar 30.
Aberrant miRNAs expression regulates the occurrence and progression of a variety of cancers, including oral squamous cell carcinoma (OSCC). This study aims to illustrate the potential effects of miR-454/nuclear receptor subfamily 3 group C member 2 (NR3C2) on the biological behaviors of OSCC cells.
GEO database was applied to detect and analyze the expression of miR-545 and NR3C2 in OSCC tissues. Two OSCC cell lines including CAL27 and Tca-83 were utilized to determine the function of miR-454/NR3C2 on OSCC cells biological behaviors. miR-454 and NR3C2 expressions were regulated by miR-454 mimic/inhibitor and pcDNA3.1-NR3C2/si-NR3C2, respectively. Cells biological behaviors were evaluated by cell proliferation, colony formation, and transwell assays.
The data collected from GEO database indicated that miR-454 expression was upregulated in OSCC tissues; however, the expression of NR3C2 assumed a downward trend. In vitro experiments, the expression trend of miR-454 in OSCC cell lines was consistent with that of the trend in tissues, and the OSCC cells growth and movement abilities significantly decreased after miR-454 depletion. Through co-transfection experiments, we explored that the abilities of OSCC cell proliferation, colony formation, invasion, and migration obviously reduced after miR-454 depletion, but these phenomena were mitigated to some extent after NR3C2 silencing.
The study illustrates that miR-454 acts as an active regulator to facilitate OSCC cells growth, colony formation, invasion, and migration by targeting NR3C2, which may afford a novel perspective and possibility for the targeted treatment of OSCC.
异常表达的 miRNA 可调节多种癌症的发生和发展,包括口腔鳞状细胞癌(OSCC)。本研究旨在阐明 miR-454/核受体亚家族 3 组 C 成员 2(NR3C2)对 OSCC 细胞生物学行为的潜在影响。
应用 GEO 数据库检测和分析 OSCC 组织中 miR-545 和 NR3C2 的表达。利用 CAL27 和 Tca-83 两种 OSCC 细胞系,确定 miR-454/NR3C2 对 OSCC 细胞生物学行为的作用。通过 miR-454 模拟物/抑制剂和 pcDNA3.1-NR3C2/si-NR3C2 分别调节 miR-454 和 NR3C2 的表达。通过细胞增殖、集落形成和 Transwell 分析评估细胞的生物学行为。
从 GEO 数据库收集的数据表明,miR-454 在 OSCC 组织中表达上调;然而,NR3C2 的表达呈下降趋势。在体外实验中,OSCC 细胞系中 miR-454 的表达趋势与组织中的趋势一致,miR-454 耗竭后 OSCC 细胞的生长和运动能力明显下降。通过共转染实验,我们发现 miR-454 耗竭后 OSCC 细胞的增殖、集落形成、侵袭和迁移能力明显降低,但 NR3C2 沉默后这些现象在一定程度上得到缓解。
本研究表明,miR-454 通过靶向 NR3C2 作为一种积极的调节剂促进 OSCC 细胞的生长、集落形成、侵袭和迁移,这可能为 OSCC 的靶向治疗提供新的视角和可能性。