MiR-338-5p suppresses proliferation, migration, invasion, and promote apoptosis of glioblastoma cells by directly targeting EFEMP1

被引:45
|
作者
Lei, Deqiang [1 ]
Zhang, Fangcheng [1 ]
Yao, Dongxiao [1 ]
Xiong, Nanxiang [1 ]
Jiang, Xiaobing [1 ]
Zhao, Hongyang [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Neurosurg, 1277 Jiefang Ave, Wuhan 430022, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Glioblastoma; Progression; MiR-338-5p; EFEMP1; TUMOR SUPPRESSION; MALIGNANT GLIOMA; CANCER-CELLS; LUNG-CANCER; IN-VIVO; FIBULIN-3; GROWTH; METHYLATION; EXPRESSION; FAMILY;
D O I
10.1016/j.biopha.2017.01.137
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective: We aimed to investigate the effect of miR-338-5p on proliferation, migration and invasion of glioblastoma (GBM) cells by regulating EFEMP1. Methods: The expression of miR-338-5p and EFEMP1 was measured by qRT-PCR and western blot. Transfection was conducted to regulate the expression of miR-338-5p and EFEMP1 in U87 cell lines. Cell proliferation, apoptosis, migration and invasion were evaluated using CCK-8 assay, flow cytometry and Transwell assay respectively. Dual luciferase reporter assay was performed to verify whether miR-338-5p directly targeted EFEMP1. Results: MiR-338-5p was significantly down-regulated in human GBM tumor tissues and cells while EFEMP1 was strongly upregulated (P < 0.05). Upregulated miR-338-5p was able to suppress cell proliferation, migration, invasion, and promote cell apoptosis in GBM cells (P < 0.05). Dual luciferase reporter gene assay determined that miR-338-5p directly targeted EFEMP1 (P < 0.05). Conclusions: MiR-338-5p suppressed proliferation, migration and invasion of GBM cells through inhibiting EFEMP1. (c) 2017 Published by Elsevier Masson SAS.
引用
收藏
页码:957 / 965
页数:9
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