MiR-146a-5 Inhibits proliferation and promotes apoptosis of oral squamous cell carcinoma cells by regulating NF-κB signaling pathway

被引:2
作者
Zhu, F-Y [1 ]
Gan, C-W [2 ]
Wang, M-X [2 ]
Sun, B-C [2 ]
Li, F-J [2 ]
Qiu, Y-H [3 ]
Wang, K. [2 ]
机构
[1] Cent South Univ, Xiangya Hosp, Oral Med Ctr, Changsha, Peoples R China
[2] Cent South Univ, Xiangya Hosp 2, Dept Oral & Maxillofacial Surg, Changsha, Peoples R China
[3] Hainan Prov Peoples Hosp, Dept Stomatol, Haikou, Hainan, Peoples R China
关键词
Oral squamous cell carcinoma; MIR-146a-5p; NIP-kappa B1; Proliferation; Apoptosis; CANCER; MICRORNAS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: The aim of this study was to investigate the function and potential mechanism of micro ribonucleic acid (miR)-146a-5p in oral squamous cell carcinoma (OSCC). MATERIALS AND METHODS: The expression of miR-146a-5p in OSCC tissues and cell lines was examined by quantitative Reverse Transcription-Polymerase Chain Reaction (qRT-PCR) analysis. Then, the role of miR-146a-5p in proliferation was analyzed by Cell Counting Kit-8 (CCK-8) assay. Besides, the proliferation and apoptosis of OSCC cells were detected by the colony formation assay and flow cytometry, respectively. Finally, the regulatory effect of miR-146a-5p/nuclear factor-kappa B subunit 1 (NF-kappa B1) was determined by Western blotting assay and Luciferase reporter assay system. RESULTS: The expression of miR-146a-5p was markedly upregulated in OSCC cell lines. In addition, the silence of miR-146a-5p inhibited the proliferation and promoted the apoptosis of OSCC cells. According to the results of the Western blotting analysis and Luciferase reporter gene assay, NF-kappa B1 was identified as a direct target of miR-146a-5p. Moreover, the downregulation of NF-kappa B1 restored the inhibitory effect of silenced miR-146a-5p on the proliferation of SCC-9 cells. CONCLUSIONS: MiR-146a-5p can inhibit the proliferation and accelerate the apoptosis of OSCC cells by directly targeting NF-kappa B1, and it plays a carcinogenic role in OSCC.
引用
收藏
页码:3717 / 3723
页数:7
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