MiR-137 silencing of BRD4 suppresses oral squamous cell carcinoma cells proliferation, migration and invasion

被引:0
作者
He, Tianpeng [1 ]
Li, Xin [1 ]
Lu, Dongsheng [1 ]
Tian, Lili [1 ]
Xu, Baohua [1 ]
机构
[1] China Japan Friendship Hosp, Dept Stomatol, 2 Yinghua East St, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-137; oral squamous cell carcinoma; BRD4; proliferation; migration; invasion; TUMOR-SUPPRESSOR; THERAPEUTIC TARGET; CANCER; METASTASIS; GROWTH; ACTS; ADENOCARCINOMA; METHYLATION; INHIBITION; EXPRESSION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: In order to study the role of miR-137 in oral squamous cell carcinoma (OSCC). Materials and methods: The gene expression level of miR-137 was detected in OSCC tissues and cell lines by using qRT-PCR. OSCC cells were transfected with miR-137 mimics and mimic controls. The proliferation, invasion and migration abilities were measured by MTT, colony formation assay, transwell and wound healing analysis. The targeting gene of miR-137 was measured by western blot, qRT-PCR and luciferase activity assays. Results: We demonstrated that the level of miR-137 was decreased in OSCC tissues when compared with the adjacent normal tissues, it also downregulated in OSCC cell lines. Overexpression of miR-137 suppressed OSCC cells proliferation, invasion and migration. In addition, we demonstrated that bromodomain 4 (BRD4) was a target gene of miR-137. Upregulation of BRD4 can ameliorate the inhibiting effect of miR-137 on tumor cells proliferation and migration. Conclusions: MiR-137 acted as an anticarcinogenic miRNA, partly through targeting BRD4 in oralsquamous cell carcinoma, it would become a therapeutic target for OSCC.
引用
收藏
页码:409 / 416
页数:8
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