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Brain Cancer Stem Cells: Current Status on Glioblastoma Multiforme

Glioblastoma multiforme (GBM), an aggressive brain tumor of astrocytic/neural stem cell origin, represents one of the most incurable cancers. GBM tumors are highly heterogeneous. However, most tumors contain a subpopulation of cells that display neural stem cell characteristics in vitro and that can...

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Detalles Bibliográficos
Autores principales: Facchino, Sabrina, Abdouh, Mohamed, Bernier, Gilbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757390/
https://www.ncbi.nlm.nih.gov/pubmed/24212782
http://dx.doi.org/10.3390/cancers3021777
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author Facchino, Sabrina
Abdouh, Mohamed
Bernier, Gilbert
author_facet Facchino, Sabrina
Abdouh, Mohamed
Bernier, Gilbert
author_sort Facchino, Sabrina
collection PubMed
description Glioblastoma multiforme (GBM), an aggressive brain tumor of astrocytic/neural stem cell origin, represents one of the most incurable cancers. GBM tumors are highly heterogeneous. However, most tumors contain a subpopulation of cells that display neural stem cell characteristics in vitro and that can generate a new brain tumor upon transplantation in mice. Hence, previously identified molecular pathways regulating neural stem cell biology were found to represent the cornerstone of GBM stem cell self-renewal mechanism. GBM tumors are also notorious for their resistance to radiation therapy. Notably, GBM “cancer stem cells” were also found to be responsible for this radioresistance. Herein, we will analyze the data supporting or not the cancer stem cell model in GBM, overview the current knowledge regarding GBM stem cell self-renewal and radioresistance molecular mechanisms, and discuss the potential therapeutic application of these findings.
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spelling pubmed-37573902013-09-04 Brain Cancer Stem Cells: Current Status on Glioblastoma Multiforme Facchino, Sabrina Abdouh, Mohamed Bernier, Gilbert Cancers (Basel) Review Glioblastoma multiforme (GBM), an aggressive brain tumor of astrocytic/neural stem cell origin, represents one of the most incurable cancers. GBM tumors are highly heterogeneous. However, most tumors contain a subpopulation of cells that display neural stem cell characteristics in vitro and that can generate a new brain tumor upon transplantation in mice. Hence, previously identified molecular pathways regulating neural stem cell biology were found to represent the cornerstone of GBM stem cell self-renewal mechanism. GBM tumors are also notorious for their resistance to radiation therapy. Notably, GBM “cancer stem cells” were also found to be responsible for this radioresistance. Herein, we will analyze the data supporting or not the cancer stem cell model in GBM, overview the current knowledge regarding GBM stem cell self-renewal and radioresistance molecular mechanisms, and discuss the potential therapeutic application of these findings. Molecular Diversity Preservation International (MDPI) 2011-03-30 /pmc/articles/PMC3757390/ /pubmed/24212782 http://dx.doi.org/10.3390/cancers3021777 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license(http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Facchino, Sabrina
Abdouh, Mohamed
Bernier, Gilbert
Brain Cancer Stem Cells: Current Status on Glioblastoma Multiforme
title Brain Cancer Stem Cells: Current Status on Glioblastoma Multiforme
title_full Brain Cancer Stem Cells: Current Status on Glioblastoma Multiforme
title_fullStr Brain Cancer Stem Cells: Current Status on Glioblastoma Multiforme
title_full_unstemmed Brain Cancer Stem Cells: Current Status on Glioblastoma Multiforme
title_short Brain Cancer Stem Cells: Current Status on Glioblastoma Multiforme
title_sort brain cancer stem cells: current status on glioblastoma multiforme
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757390/
https://www.ncbi.nlm.nih.gov/pubmed/24212782
http://dx.doi.org/10.3390/cancers3021777
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