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MicroRNA-203 As a Stemness Inhibitor of Glioblastoma Stem Cells

Glioblastoma stem cells (GBM-SCs) are believed to be a subpopulation within all glioblastoma (GBM) cells that are in large part responsible for tumor growth and the high grade of therapeutic resistance that is so characteristic of GBM. MicroRNAs (miR) have been implicated in regulating the expressio...

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Autores principales: Deng, Yifan, Zhu, Gang, Luo, Honghai, Zhao, Shiguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Molecular and Cellular Biology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990754/
https://www.ncbi.nlm.nih.gov/pubmed/27484906
http://dx.doi.org/10.14348/molcells.2016.0118
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author Deng, Yifan
Zhu, Gang
Luo, Honghai
Zhao, Shiguang
author_facet Deng, Yifan
Zhu, Gang
Luo, Honghai
Zhao, Shiguang
author_sort Deng, Yifan
collection PubMed
description Glioblastoma stem cells (GBM-SCs) are believed to be a subpopulation within all glioblastoma (GBM) cells that are in large part responsible for tumor growth and the high grade of therapeutic resistance that is so characteristic of GBM. MicroRNAs (miR) have been implicated in regulating the expression of oncogenes and tumor suppressor genes in cancer stem cells, including GBM-SCs, and they are a potential target for cancer therapy. In the current study, miR-203 expression was reduced in CD133(+) GBM-SCs derived from six human GBM biopsies. MicroRNA-203 transfected GBM-SCs had reduced capacity for self-renewal in the cell sphere assay and increased expression of glial and neuronal differentiation markers. In addition, a reduced proliferation rate and an increased rate of apoptosis were observed. Therefore, miR-203 has the potential to reduce features of stemness, specifically in GBM-SCs, and is a logical target for GBM gene therapy.
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spelling pubmed-49907542016-09-01 MicroRNA-203 As a Stemness Inhibitor of Glioblastoma Stem Cells Deng, Yifan Zhu, Gang Luo, Honghai Zhao, Shiguang Mol Cells Article Glioblastoma stem cells (GBM-SCs) are believed to be a subpopulation within all glioblastoma (GBM) cells that are in large part responsible for tumor growth and the high grade of therapeutic resistance that is so characteristic of GBM. MicroRNAs (miR) have been implicated in regulating the expression of oncogenes and tumor suppressor genes in cancer stem cells, including GBM-SCs, and they are a potential target for cancer therapy. In the current study, miR-203 expression was reduced in CD133(+) GBM-SCs derived from six human GBM biopsies. MicroRNA-203 transfected GBM-SCs had reduced capacity for self-renewal in the cell sphere assay and increased expression of glial and neuronal differentiation markers. In addition, a reduced proliferation rate and an increased rate of apoptosis were observed. Therefore, miR-203 has the potential to reduce features of stemness, specifically in GBM-SCs, and is a logical target for GBM gene therapy. Korean Society for Molecular and Cellular Biology 2016-08-31 2016-08-03 /pmc/articles/PMC4990754/ /pubmed/27484906 http://dx.doi.org/10.14348/molcells.2016.0118 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/.
spellingShingle Article
Deng, Yifan
Zhu, Gang
Luo, Honghai
Zhao, Shiguang
MicroRNA-203 As a Stemness Inhibitor of Glioblastoma Stem Cells
title MicroRNA-203 As a Stemness Inhibitor of Glioblastoma Stem Cells
title_full MicroRNA-203 As a Stemness Inhibitor of Glioblastoma Stem Cells
title_fullStr MicroRNA-203 As a Stemness Inhibitor of Glioblastoma Stem Cells
title_full_unstemmed MicroRNA-203 As a Stemness Inhibitor of Glioblastoma Stem Cells
title_short MicroRNA-203 As a Stemness Inhibitor of Glioblastoma Stem Cells
title_sort microrna-203 as a stemness inhibitor of glioblastoma stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990754/
https://www.ncbi.nlm.nih.gov/pubmed/27484906
http://dx.doi.org/10.14348/molcells.2016.0118
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