MiR-9-5p Inhibits Glioblastoma Cells Proliferation Through Directly Targeting FOXP2 (Forkhead Box P2)

Glioblastoma (GBM) is the most malignant tumor in the central nervous system and the treatment is still unsatisfactory because the mechanism of the disease remains unclear. The abnormal expression of miRNAs and its target proteins play a crucial role in the development of glioblastoma. In this study...

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Published inFrontiers in oncology Vol. 9; p. 1176
Main Authors Zhang, Hongbo, Li, Yuntao, Tan, Yinqiu, Liu, Qi, Jiang, Shuting, Liu, Dongyuan, Chen, Qianxue, Zhang, Shizhong
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 19.11.2019
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Summary:Glioblastoma (GBM) is the most malignant tumor in the central nervous system and the treatment is still unsatisfactory because the mechanism of the disease remains unclear. The abnormal expression of miRNAs and its target proteins play a crucial role in the development of glioblastoma. In this study, we demonstrated that high expression of miR-9-5p and low expression of forkhead box P2 (FOXP2) were related with better outcome in patients with GBM, and down regulated FOXP2 expression was able to inhibit glioma cells proliferation by cell cycle arrest. Furthermore, we found that FOXP2 was the target protein of miR-9-5p in luciferase assay. The results of this study suggest a novel regulatory mechanism that miR-9-5p can inhibit glioma cells proliferation by downregulating FOXP2.
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Edited by: Liam Chen, Johns Hopkins University, United States
Reviewed by: Kamalakannan Palanichamy, The Ohio State University, United States; Akira Asai, University of Shizuoka, Japan
These authors have contributed equally to this work
This article was submitted to Neuro-Oncology and Neurosurgical Oncology, a section of the journal Frontiers in Oncology
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2019.01176