Oncotarget

Research Papers:

miR-204 suppresses the development and progression of human glioblastoma by targeting ATF2

Shiwei Song _, Abul Fajol, Xiankun Tu, Baogang Ren and Songsheng Shi

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Oncotarget. 2016; 7:70058-70065. https://doi.org/10.18632/oncotarget.11732

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Abstract

Shiwei Song1, Abul Fajol2, Xiankun Tu1, Baogang Ren1, Songsheng Shi1

1Department of Neurosurgery, Fujian Medical University Affiliated Union Hospital, Fujian Neurosurgical Institute, Fuzhou, 350001, China

2Department of Clinical Sciences, CRC, Lund University, Malmö, 20502, Sweden

Correspondence to:

Shiwei Song, email: songshiweifmu@163.com

Keywords: miR-204, GBM, suppressor

Received: June 21, 2016     Accepted: August 16, 2016     Published: August 31, 2016

ABSTRACT

In human cancers, miRNAs are important regulators of multiple cellular processes, and aberrant miRNA expression has been observed, and their alterations contribute to multiple cancer development and progression. Till now, little has been known about the role of miR-204 in human glioblastoma (GBM). In the present study, we used in-vitro assays to investigate the mechanisms of miR-204 in GBM cell lines and 60 cases of GBM tissues. Here, we found that miR-204 expression is downregulated in both GBM cell lines A172, U87 and U251 cells and GBM tissues as compared with NHA cells and normal tissues (all p<0.001). In addition, the ectopic expression of miR-204 suppressed A172 and U87 cell proliferation, migration and invasion. Meanwhile, miR-204 over-expression extremely inhibited the protein expression of ATF2. Notably, the enforced expression of ATF2 in A172 and U87 cells with the over-expression of miR-204 attenuated the inhibitory effects of miR-204 on proliferation, migration and invasion. In conclusion, our findings suggest that miR-204 suppressed cell proliferation, migration and invasion through inhibition of ATF2, thus, miR-204 may function as a useful drug target in the treatment and diagnosis of GBM.


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