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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Main Authors: Hongbo Zhang, Yuntao Li, Yinqiu Tan, Qi Liu, Shuting Jiang, Dongyuan Liu, Qianxue Chen, Shizhong Zhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-11-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fonc.2019.01176/full
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author Hongbo Zhang
Hongbo Zhang
Yuntao Li
Yuntao Li
Yinqiu Tan
Qi Liu
Shuting Jiang
Dongyuan Liu
Qianxue Chen
Shizhong Zhang
Shizhong Zhang
author_facet Hongbo Zhang
Hongbo Zhang
Yuntao Li
Yuntao Li
Yinqiu Tan
Qi Liu
Shuting Jiang
Dongyuan Liu
Qianxue Chen
Shizhong Zhang
Shizhong Zhang
author_sort Hongbo Zhang
collection DOAJ
description 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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spelling doaj.art-99561c85e7794f2aa695721f7fcbf9892022-12-21T18:59:26ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2019-11-01910.3389/fonc.2019.01176470675MiR-9-5p Inhibits Glioblastoma Cells Proliferation Through Directly Targeting FOXP2 (Forkhead Box P2)Hongbo Zhang0Hongbo Zhang1Yuntao Li2Yuntao Li3Yinqiu Tan4Qi Liu5Shuting Jiang6Dongyuan Liu7Qianxue Chen8Shizhong Zhang9Shizhong Zhang10Department of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou, ChinaGuangdong Provincial Key Laboratory on Brain Function Repair and Regeneration, The National Key Clinic Specialty, The Engineering Technology Research Center of Education Ministry of China, The Neurosurgery Institute of Guangdong Province, Southern Medical University, Guangzhou, ChinaDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, ChinaDepartment of Neurosurgery, Huzhou Central Hospital, Zhejiang University School of Medicine, Huzhou, ChinaDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, ChinaDepartment of Rheumatology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, ChinaDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, ChinaDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, ChinaDepartment of Neurosurgery, Renmin Hospital of Wuhan University, Wuhan, ChinaDepartment of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou, ChinaGuangdong Provincial Key Laboratory on Brain Function Repair and Regeneration, The National Key Clinic Specialty, The Engineering Technology Research Center of Education Ministry of China, The Neurosurgery Institute of Guangdong Province, Southern Medical University, Guangzhou, ChinaGlioblastoma (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.https://www.frontiersin.org/article/10.3389/fonc.2019.01176/fullmiR-9-5pFOXP2glioblastomaproliferationglioma
spellingShingle Hongbo Zhang
Hongbo Zhang
Yuntao Li
Yuntao Li
Yinqiu Tan
Qi Liu
Shuting Jiang
Dongyuan Liu
Qianxue Chen
Shizhong Zhang
Shizhong Zhang
MiR-9-5p Inhibits Glioblastoma Cells Proliferation Through Directly Targeting FOXP2 (Forkhead Box P2)
Frontiers in Oncology
miR-9-5p
FOXP2
glioblastoma
proliferation
glioma
title MiR-9-5p Inhibits Glioblastoma Cells Proliferation Through Directly Targeting FOXP2 (Forkhead Box P2)
title_full MiR-9-5p Inhibits Glioblastoma Cells Proliferation Through Directly Targeting FOXP2 (Forkhead Box P2)
title_fullStr MiR-9-5p Inhibits Glioblastoma Cells Proliferation Through Directly Targeting FOXP2 (Forkhead Box P2)
title_full_unstemmed MiR-9-5p Inhibits Glioblastoma Cells Proliferation Through Directly Targeting FOXP2 (Forkhead Box P2)
title_short MiR-9-5p Inhibits Glioblastoma Cells Proliferation Through Directly Targeting FOXP2 (Forkhead Box P2)
title_sort mir 9 5p inhibits glioblastoma cells proliferation through directly targeting foxp2 forkhead box p2
topic miR-9-5p
FOXP2
glioblastoma
proliferation
glioma
url https://www.frontiersin.org/article/10.3389/fonc.2019.01176/full
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