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The NFκB pathway: a therapeutic target in glioblastoma

Cancer initiating cells have been described to be the only cell population with tumorigenic capacity in glioblastoma multiforme, one of the most aggressive and untreatable cancers. Recent work from our group described that NFκB pathway was activated in glioblastoma initiating cells undergo...

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Autores principales: Nogueira, Lorena, Ruiz-Ontañon, Patricia, Vazquez-Barquero, Alfonso, Moris, Francisco, Fernandez-Luna, Jose L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248209/
https://www.ncbi.nlm.nih.gov/pubmed/21896960
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author Nogueira, Lorena
Ruiz-Ontañon, Patricia
Vazquez-Barquero, Alfonso
Moris, Francisco
Fernandez-Luna, Jose L.
author_facet Nogueira, Lorena
Ruiz-Ontañon, Patricia
Vazquez-Barquero, Alfonso
Moris, Francisco
Fernandez-Luna, Jose L.
author_sort Nogueira, Lorena
collection PubMed
description Cancer initiating cells have been described to be the only cell population with tumorigenic capacity in glioblastoma multiforme, one of the most aggressive and untreatable cancers. Recent work from our group described that NFκB pathway was activated in glioblastoma initiating cells undergoing differentiation, and that blockade of this activation promoted senescence of differentiating cells. NFκB activation in cancer may be the result of either exposure to proinflammatory stimuli in the tumor microenvironment or upregulation of the signaling pathway by upstream regulators. Appropriate control of NFκB activity, which can be achieved by gene modification or pharmacological strategies, would provide a potential approach for the management of NFκB related tumors, including glioblastoma. Here, we summarize the current knowledge of the relevance of NFκB in cancer and its possible role as a target of therapeutic intervention.
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spelling pubmed-32482092012-01-18 The NFκB pathway: a therapeutic target in glioblastoma Nogueira, Lorena Ruiz-Ontañon, Patricia Vazquez-Barquero, Alfonso Moris, Francisco Fernandez-Luna, Jose L. Oncotarget Research Perspectives Cancer initiating cells have been described to be the only cell population with tumorigenic capacity in glioblastoma multiforme, one of the most aggressive and untreatable cancers. Recent work from our group described that NFκB pathway was activated in glioblastoma initiating cells undergoing differentiation, and that blockade of this activation promoted senescence of differentiating cells. NFκB activation in cancer may be the result of either exposure to proinflammatory stimuli in the tumor microenvironment or upregulation of the signaling pathway by upstream regulators. Appropriate control of NFκB activity, which can be achieved by gene modification or pharmacological strategies, would provide a potential approach for the management of NFκB related tumors, including glioblastoma. Here, we summarize the current knowledge of the relevance of NFκB in cancer and its possible role as a target of therapeutic intervention. Impact Journals LLC 2011-09-05 /pmc/articles/PMC3248209/ /pubmed/21896960 Text en Copyright: © 2011 Nogueira et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Research Perspectives
Nogueira, Lorena
Ruiz-Ontañon, Patricia
Vazquez-Barquero, Alfonso
Moris, Francisco
Fernandez-Luna, Jose L.
The NFκB pathway: a therapeutic target in glioblastoma
title The NFκB pathway: a therapeutic target in glioblastoma
title_full The NFκB pathway: a therapeutic target in glioblastoma
title_fullStr The NFκB pathway: a therapeutic target in glioblastoma
title_full_unstemmed The NFκB pathway: a therapeutic target in glioblastoma
title_short The NFκB pathway: a therapeutic target in glioblastoma
title_sort nfκb pathway: a therapeutic target in glioblastoma
topic Research Perspectives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248209/
https://www.ncbi.nlm.nih.gov/pubmed/21896960
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