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Microglia and Macrophages in Malignant Gliomas: Recent Discoveries and Implications for Promising Therapies

Malignant gliomas are the most common primary brain tumors. Their deadliest manifestation, glioblastoma multiforme (GBM), accounts for 15% of all primary brain tumors and is associated with a median survival of only 15 months even after multimodal therapy. There is substantial presence of microglia...

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Detalles Bibliográficos
Autores principales: Carvalho da Fonseca, Anna Carolina, Badie, Behnam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707269/
https://www.ncbi.nlm.nih.gov/pubmed/23864876
http://dx.doi.org/10.1155/2013/264124
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author Carvalho da Fonseca, Anna Carolina
Badie, Behnam
author_facet Carvalho da Fonseca, Anna Carolina
Badie, Behnam
author_sort Carvalho da Fonseca, Anna Carolina
collection PubMed
description Malignant gliomas are the most common primary brain tumors. Their deadliest manifestation, glioblastoma multiforme (GBM), accounts for 15% of all primary brain tumors and is associated with a median survival of only 15 months even after multimodal therapy. There is substantial presence of microglia and macrophages within and surrounding brain tumors. These immune cells acquire an alternatively activated phenotype with potent tumor-tropic functions that contribute to glioma growth and invasion. In this review, we briefly summarize recent data that has been reported on the interaction of microglia/macrophages with brain tumors and discuss potential application of these findings to the development of future antiglioma therapies.
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spelling pubmed-37072692013-07-17 Microglia and Macrophages in Malignant Gliomas: Recent Discoveries and Implications for Promising Therapies Carvalho da Fonseca, Anna Carolina Badie, Behnam Clin Dev Immunol Review Article Malignant gliomas are the most common primary brain tumors. Their deadliest manifestation, glioblastoma multiforme (GBM), accounts for 15% of all primary brain tumors and is associated with a median survival of only 15 months even after multimodal therapy. There is substantial presence of microglia and macrophages within and surrounding brain tumors. These immune cells acquire an alternatively activated phenotype with potent tumor-tropic functions that contribute to glioma growth and invasion. In this review, we briefly summarize recent data that has been reported on the interaction of microglia/macrophages with brain tumors and discuss potential application of these findings to the development of future antiglioma therapies. Hindawi Publishing Corporation 2013 2013-06-25 /pmc/articles/PMC3707269/ /pubmed/23864876 http://dx.doi.org/10.1155/2013/264124 Text en Copyright © 2013 A. C. Carvalho da Fonseca and B. Badie. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Carvalho da Fonseca, Anna Carolina
Badie, Behnam
Microglia and Macrophages in Malignant Gliomas: Recent Discoveries and Implications for Promising Therapies
title Microglia and Macrophages in Malignant Gliomas: Recent Discoveries and Implications for Promising Therapies
title_full Microglia and Macrophages in Malignant Gliomas: Recent Discoveries and Implications for Promising Therapies
title_fullStr Microglia and Macrophages in Malignant Gliomas: Recent Discoveries and Implications for Promising Therapies
title_full_unstemmed Microglia and Macrophages in Malignant Gliomas: Recent Discoveries and Implications for Promising Therapies
title_short Microglia and Macrophages in Malignant Gliomas: Recent Discoveries and Implications for Promising Therapies
title_sort microglia and macrophages in malignant gliomas: recent discoveries and implications for promising therapies
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707269/
https://www.ncbi.nlm.nih.gov/pubmed/23864876
http://dx.doi.org/10.1155/2013/264124
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