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SOX7 inhibits tumor progression of glioblastoma and is regulated by miRNA-24

OBJECTIVE: Sex-determining region Y-box 7 (SOX7) is a putative tumor suppressor in various types of human cancers. In the present study, the expression and function of SOX7 was investigated in human glioblastoma (GBM) cells. METHODS: Real-time PCR and western blot were carried out to reveal the expr...

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Detalles Bibliográficos
Autores principales: Xiuju, Chen, Zhen, Wang, Yanchao, Shi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter Open 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5329813/
https://www.ncbi.nlm.nih.gov/pubmed/28352781
http://dx.doi.org/10.1515/med-2016-0026
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author Xiuju, Chen
Zhen, Wang
Yanchao, Shi
author_facet Xiuju, Chen
Zhen, Wang
Yanchao, Shi
author_sort Xiuju, Chen
collection PubMed
description OBJECTIVE: Sex-determining region Y-box 7 (SOX7) is a putative tumor suppressor in various types of human cancers. In the present study, the expression and function of SOX7 was investigated in human glioblastoma (GBM) cells. METHODS: Real-time PCR and western blot were carried out to reveal the expression of SOX7 in GBM specimens and cultured cell lines. A short interfering RNA (siRNA) targeting SOX7 was synthesized and transfected into U87 cells. 3-(4,5-Dimethylthiazol-2-yl)- 2,5-diphenyltetrazolium bromide (MTT) assay was performed to valuate the cell proliferation ability in U87 cells. Bioinformatics analysis further predicted its regulation by microRNA-24 (miR-24). Luciferase reporter assay was performed to prove this regulation. RESULTS: SOX7 was downregulated in GBM specimens and cell lines. Inhibition of SOX7 in cultured U87 cells resulted in a slower growth rate. Mechanically, SOX7 was a target of miR-24, demonstrated by reporter assay. CONCLUSION: SOX7 was a strong tumor suppressor regulated by miR-24 in human GBM cells.
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spelling pubmed-53298132017-03-28 SOX7 inhibits tumor progression of glioblastoma and is regulated by miRNA-24 Xiuju, Chen Zhen, Wang Yanchao, Shi Open Med (Wars) Research Article OBJECTIVE: Sex-determining region Y-box 7 (SOX7) is a putative tumor suppressor in various types of human cancers. In the present study, the expression and function of SOX7 was investigated in human glioblastoma (GBM) cells. METHODS: Real-time PCR and western blot were carried out to reveal the expression of SOX7 in GBM specimens and cultured cell lines. A short interfering RNA (siRNA) targeting SOX7 was synthesized and transfected into U87 cells. 3-(4,5-Dimethylthiazol-2-yl)- 2,5-diphenyltetrazolium bromide (MTT) assay was performed to valuate the cell proliferation ability in U87 cells. Bioinformatics analysis further predicted its regulation by microRNA-24 (miR-24). Luciferase reporter assay was performed to prove this regulation. RESULTS: SOX7 was downregulated in GBM specimens and cell lines. Inhibition of SOX7 in cultured U87 cells resulted in a slower growth rate. Mechanically, SOX7 was a target of miR-24, demonstrated by reporter assay. CONCLUSION: SOX7 was a strong tumor suppressor regulated by miR-24 in human GBM cells. De Gruyter Open 2016-05-06 /pmc/articles/PMC5329813/ /pubmed/28352781 http://dx.doi.org/10.1515/med-2016-0026 Text en © 2016 Wang Zhen et al. http://creativecommons.org/licenses/by-nc-nd/3.0 This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
spellingShingle Research Article
Xiuju, Chen
Zhen, Wang
Yanchao, Shi
SOX7 inhibits tumor progression of glioblastoma and is regulated by miRNA-24
title SOX7 inhibits tumor progression of glioblastoma and is regulated by miRNA-24
title_full SOX7 inhibits tumor progression of glioblastoma and is regulated by miRNA-24
title_fullStr SOX7 inhibits tumor progression of glioblastoma and is regulated by miRNA-24
title_full_unstemmed SOX7 inhibits tumor progression of glioblastoma and is regulated by miRNA-24
title_short SOX7 inhibits tumor progression of glioblastoma and is regulated by miRNA-24
title_sort sox7 inhibits tumor progression of glioblastoma and is regulated by mirna-24
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5329813/
https://www.ncbi.nlm.nih.gov/pubmed/28352781
http://dx.doi.org/10.1515/med-2016-0026
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