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Cell of Origin and Cancer Stem Cells in Tumor Suppressor Mouse Models of Glioblastoma

The cellular origins and the mechanisms of progression, maintenance of tumorigenicity, and therapeutic resistance are central questions in the glioblastoma multiforme (GBM) field. Using tumor suppressor mouse models, our group recently reported two independent populations of adult GBM-initiating cen...

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Autores principales: Alcantara Llaguno, Sheila R., Xie, Xuanhua, Parada, Luis F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353557/
https://www.ncbi.nlm.nih.gov/pubmed/27815542
http://dx.doi.org/10.1101/sqb.2016.81.030973
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author Alcantara Llaguno, Sheila R.
Xie, Xuanhua
Parada, Luis F.
author_facet Alcantara Llaguno, Sheila R.
Xie, Xuanhua
Parada, Luis F.
author_sort Alcantara Llaguno, Sheila R.
collection PubMed
description The cellular origins and the mechanisms of progression, maintenance of tumorigenicity, and therapeutic resistance are central questions in the glioblastoma multiforme (GBM) field. Using tumor suppressor mouse models, our group recently reported two independent populations of adult GBM-initiating central nervous system progenitors. We found different functional and molecular subtypes depending on the tumor-initiating cell lineage, indicating that the cell of origin is a driver of GBM subtype diversity. Using an in vivo model, we also showed that GBM cancer stem cells (CSCs) or glioma stem cells (GSCs) contribute to resistance to chemotherapeutic agents and that genetic ablation of GSCs leads to a delay in tumor progression. These studies are consistent with the cell of origin and CSCs as critical regulators of the pathogenesis of GBM.
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spelling pubmed-63535572019-01-30 Cell of Origin and Cancer Stem Cells in Tumor Suppressor Mouse Models of Glioblastoma Alcantara Llaguno, Sheila R. Xie, Xuanhua Parada, Luis F. Cold Spring Harb Symp Quant Biol Article The cellular origins and the mechanisms of progression, maintenance of tumorigenicity, and therapeutic resistance are central questions in the glioblastoma multiforme (GBM) field. Using tumor suppressor mouse models, our group recently reported two independent populations of adult GBM-initiating central nervous system progenitors. We found different functional and molecular subtypes depending on the tumor-initiating cell lineage, indicating that the cell of origin is a driver of GBM subtype diversity. Using an in vivo model, we also showed that GBM cancer stem cells (CSCs) or glioma stem cells (GSCs) contribute to resistance to chemotherapeutic agents and that genetic ablation of GSCs leads to a delay in tumor progression. These studies are consistent with the cell of origin and CSCs as critical regulators of the pathogenesis of GBM. 2016-11-04 2016 /pmc/articles/PMC6353557/ /pubmed/27815542 http://dx.doi.org/10.1101/sqb.2016.81.030973 Text en http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial License, which permits reuse and redistribution, except for commercial purposes, provided that the original author and source are credited.
spellingShingle Article
Alcantara Llaguno, Sheila R.
Xie, Xuanhua
Parada, Luis F.
Cell of Origin and Cancer Stem Cells in Tumor Suppressor Mouse Models of Glioblastoma
title Cell of Origin and Cancer Stem Cells in Tumor Suppressor Mouse Models of Glioblastoma
title_full Cell of Origin and Cancer Stem Cells in Tumor Suppressor Mouse Models of Glioblastoma
title_fullStr Cell of Origin and Cancer Stem Cells in Tumor Suppressor Mouse Models of Glioblastoma
title_full_unstemmed Cell of Origin and Cancer Stem Cells in Tumor Suppressor Mouse Models of Glioblastoma
title_short Cell of Origin and Cancer Stem Cells in Tumor Suppressor Mouse Models of Glioblastoma
title_sort cell of origin and cancer stem cells in tumor suppressor mouse models of glioblastoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353557/
https://www.ncbi.nlm.nih.gov/pubmed/27815542
http://dx.doi.org/10.1101/sqb.2016.81.030973
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