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The complement system in glioblastoma multiforme
The human complement system is represents the main effector arm of innate immunity and its ambivalent function in cancer has been subject of ongoing dispute. Glioma stem-like cells (GSC) residing in specific niches within glioblastomas (GBM) are capable of self-renewal and tumor proliferation. Recen...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134703/ https://www.ncbi.nlm.nih.gov/pubmed/30208949 http://dx.doi.org/10.1186/s40478-018-0591-4 |
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author | Bouwens van der Vlis, T. A. M. Kros, J. M. Mustafa, D. A. M. van Wijck, R. T. A. Ackermans, L. van Hagen, P. M. van der Spek, P. J. |
author_facet | Bouwens van der Vlis, T. A. M. Kros, J. M. Mustafa, D. A. M. van Wijck, R. T. A. Ackermans, L. van Hagen, P. M. van der Spek, P. J. |
author_sort | Bouwens van der Vlis, T. A. M. |
collection | PubMed |
description | The human complement system is represents the main effector arm of innate immunity and its ambivalent function in cancer has been subject of ongoing dispute. Glioma stem-like cells (GSC) residing in specific niches within glioblastomas (GBM) are capable of self-renewal and tumor proliferation. Recent data are indicative of the influence of the complement system on the maintenance of these cells. It appears that the role of the complement system in glial tumorigenesis, particularly its influence on GSC niches and GSC maintenance, is significant and warrants further exploration for therapeutic interventions. |
format | Online Article Text |
id | pubmed-6134703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61347032018-09-13 The complement system in glioblastoma multiforme Bouwens van der Vlis, T. A. M. Kros, J. M. Mustafa, D. A. M. van Wijck, R. T. A. Ackermans, L. van Hagen, P. M. van der Spek, P. J. Acta Neuropathol Commun Review The human complement system is represents the main effector arm of innate immunity and its ambivalent function in cancer has been subject of ongoing dispute. Glioma stem-like cells (GSC) residing in specific niches within glioblastomas (GBM) are capable of self-renewal and tumor proliferation. Recent data are indicative of the influence of the complement system on the maintenance of these cells. It appears that the role of the complement system in glial tumorigenesis, particularly its influence on GSC niches and GSC maintenance, is significant and warrants further exploration for therapeutic interventions. BioMed Central 2018-09-12 /pmc/articles/PMC6134703/ /pubmed/30208949 http://dx.doi.org/10.1186/s40478-018-0591-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Bouwens van der Vlis, T. A. M. Kros, J. M. Mustafa, D. A. M. van Wijck, R. T. A. Ackermans, L. van Hagen, P. M. van der Spek, P. J. The complement system in glioblastoma multiforme |
title | The complement system in glioblastoma multiforme |
title_full | The complement system in glioblastoma multiforme |
title_fullStr | The complement system in glioblastoma multiforme |
title_full_unstemmed | The complement system in glioblastoma multiforme |
title_short | The complement system in glioblastoma multiforme |
title_sort | complement system in glioblastoma multiforme |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134703/ https://www.ncbi.nlm.nih.gov/pubmed/30208949 http://dx.doi.org/10.1186/s40478-018-0591-4 |
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