Cargando…
Functional invadopodia formed in glioblastoma stem cells are important regulators of tumor angiogenesis
Glioblastoma (GBM) represents the most common and lethal brain tumor. High vascularization, necrosis and invasiveness are hallmarks of GBM aggressiveness with recent data suggesting the important role of glioblastoma stem cells (GSCs) in these processes. It is now well established that cancer cells...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945526/ https://www.ncbi.nlm.nih.gov/pubmed/29755678 http://dx.doi.org/10.18632/oncotarget.25045 |
_version_ | 1783322006990618624 |
---|---|
author | Petropoulos, Christos Guichet, Pierre-Olivier Masliantsev, Konstantin Wager, Michel Karayan-Tapon, Lucie |
author_facet | Petropoulos, Christos Guichet, Pierre-Olivier Masliantsev, Konstantin Wager, Michel Karayan-Tapon, Lucie |
author_sort | Petropoulos, Christos |
collection | PubMed |
description | Glioblastoma (GBM) represents the most common and lethal brain tumor. High vascularization, necrosis and invasiveness are hallmarks of GBM aggressiveness with recent data suggesting the important role of glioblastoma stem cells (GSCs) in these processes. It is now well established that cancer cells employ specialized structures termed invadosomes to potentiate invasion. However, the role of these structures in GBM dissemination remains poorly investigated. In this study, we showed that GBM-isolated GSCs form invadopodia-like protrusions endowed with degradative action. Interestingly, their formation depends on extracellular matrix (ECM) sensing via the CD44 receptor. We also found that GSCs invasive migration occurring during tubes assembly is promoted through invadopodia-mediated-ECM remodeling and LIM kinases signaling. Moreover, our study demonstrates that GSCs are highly adaptable cells that are able not only to restore damaged endothelial-derived tubes but also to generate in cooperation with normal endothelial cells (ECs) intact vascular channels. Taken together, our data provide new insights in GBM microvasculature and suggest that GSCs targeting in combination with anti-VEGF therapy may block tumor progression. |
format | Online Article Text |
id | pubmed-5945526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-59455262018-05-13 Functional invadopodia formed in glioblastoma stem cells are important regulators of tumor angiogenesis Petropoulos, Christos Guichet, Pierre-Olivier Masliantsev, Konstantin Wager, Michel Karayan-Tapon, Lucie Oncotarget Research Paper Glioblastoma (GBM) represents the most common and lethal brain tumor. High vascularization, necrosis and invasiveness are hallmarks of GBM aggressiveness with recent data suggesting the important role of glioblastoma stem cells (GSCs) in these processes. It is now well established that cancer cells employ specialized structures termed invadosomes to potentiate invasion. However, the role of these structures in GBM dissemination remains poorly investigated. In this study, we showed that GBM-isolated GSCs form invadopodia-like protrusions endowed with degradative action. Interestingly, their formation depends on extracellular matrix (ECM) sensing via the CD44 receptor. We also found that GSCs invasive migration occurring during tubes assembly is promoted through invadopodia-mediated-ECM remodeling and LIM kinases signaling. Moreover, our study demonstrates that GSCs are highly adaptable cells that are able not only to restore damaged endothelial-derived tubes but also to generate in cooperation with normal endothelial cells (ECs) intact vascular channels. Taken together, our data provide new insights in GBM microvasculature and suggest that GSCs targeting in combination with anti-VEGF therapy may block tumor progression. Impact Journals LLC 2018-04-17 /pmc/articles/PMC5945526/ /pubmed/29755678 http://dx.doi.org/10.18632/oncotarget.25045 Text en Copyright: © 2018 Petropoulos et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Petropoulos, Christos Guichet, Pierre-Olivier Masliantsev, Konstantin Wager, Michel Karayan-Tapon, Lucie Functional invadopodia formed in glioblastoma stem cells are important regulators of tumor angiogenesis |
title | Functional invadopodia formed in glioblastoma stem cells are important regulators of tumor angiogenesis |
title_full | Functional invadopodia formed in glioblastoma stem cells are important regulators of tumor angiogenesis |
title_fullStr | Functional invadopodia formed in glioblastoma stem cells are important regulators of tumor angiogenesis |
title_full_unstemmed | Functional invadopodia formed in glioblastoma stem cells are important regulators of tumor angiogenesis |
title_short | Functional invadopodia formed in glioblastoma stem cells are important regulators of tumor angiogenesis |
title_sort | functional invadopodia formed in glioblastoma stem cells are important regulators of tumor angiogenesis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945526/ https://www.ncbi.nlm.nih.gov/pubmed/29755678 http://dx.doi.org/10.18632/oncotarget.25045 |
work_keys_str_mv | AT petropouloschristos functionalinvadopodiaformedinglioblastomastemcellsareimportantregulatorsoftumorangiogenesis AT guichetpierreolivier functionalinvadopodiaformedinglioblastomastemcellsareimportantregulatorsoftumorangiogenesis AT masliantsevkonstantin functionalinvadopodiaformedinglioblastomastemcellsareimportantregulatorsoftumorangiogenesis AT wagermichel functionalinvadopodiaformedinglioblastomastemcellsareimportantregulatorsoftumorangiogenesis AT karayantaponlucie functionalinvadopodiaformedinglioblastomastemcellsareimportantregulatorsoftumorangiogenesis |