Overexpression of miR-1283 Inhibits Cell Proliferation and Invasion of Glioma Cells by Targeting ATF4

被引:20
|
作者
Chen, Hao [1 ]
Zhang, Yi [1 ]
Su, Hai [1 ]
Shi, Hui [1 ]
Xiong, Qijiang [1 ]
Su, Zulu [1 ]
机构
[1] Chongqing Med Univ, Dept Neurosurg, Yongchuan Hosp, 439 Xuanhua Ro, Chongqing 402160, Peoples R China
关键词
Glioma; MicroRNA-1283; Activating transcription factor 4 (ATF4); Proliferation; Invasion; ACTIVATING TRANSCRIPTION FACTOR-4; MATRIX-METALLOPROTEINASE; CANCER; PROMOTES; EXPRESSION; ANGIOGENESIS; MECHANISMS; RESISTANCE; MICRORNAS; INCREASES;
D O I
10.3727/096504018X15251282086836
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It is well known that activating transcription factor 4 (ATF4) expression is closely associated with progression of many cancers. We found that miR-1283 could directly target ATF4. However, the precise mechanisms of miR-1283 in glioma have not been well clarified. Our study aimed to explore the interaction between ATF4 and miR-1283 in glioma. In this study, we found that the level of miR-1283 was dramatically decreased in glioma tissues and cell lines, the expression of ATF4 was significantly increased, and the low level of miR-1283 was closely associated with high expression of ATF4 in glioma tissues. Moreover, introduction of miR-1283 significantly inhibited proliferation and invasion of glioma cells. However, knockdown of miR-1283 promoted the proliferation and invasion in glioma cells. Bioinformatics analysis predicted that the ATF4 was a potential target gene of miR-1283. Luciferase reporter assay demonstrated that miR-1283 could directly target ATF4. In addition, knockdown of ATF4 had similar effects with miR-1283 ovcrexpression on glioma cells. Upregulation of ATF4 in glioma cells partially reversed the inhibitory effects of miR-1283 mimic. Overexpression of miR-1283 inhibited cell proliferation and invasion of glioma cells by directly downregulating ATF4 expression.
引用
收藏
页码:325 / 334
页数:10
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