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Pericyte–Glioblastoma Cell Interaction: A Key Target to Prevent Glioblastoma Progression

Multiple biological processes rely on direct intercellular interactions to regulate cell proliferation and migration in embryonic development and cancer processes. Tumor development and growth depends on close interactions between cancer cells and cells in the tumor microenvironment. During embryoni...

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Autores principales: Pombero, Ana, Garcia-Lopez, Raquel, Martínez, Salvador
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177553/
https://www.ncbi.nlm.nih.gov/pubmed/37174724
http://dx.doi.org/10.3390/cells12091324
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author Pombero, Ana
Garcia-Lopez, Raquel
Martínez, Salvador
author_facet Pombero, Ana
Garcia-Lopez, Raquel
Martínez, Salvador
author_sort Pombero, Ana
collection PubMed
description Multiple biological processes rely on direct intercellular interactions to regulate cell proliferation and migration in embryonic development and cancer processes. Tumor development and growth depends on close interactions between cancer cells and cells in the tumor microenvironment. During embryonic development, morphogenetic signals and direct cell contacts control cell proliferation, polarity, and morphogenesis. Cancer cells communicate with cells in the tumor niche through molecular signals and intercellular contacts, thereby modifying the vascular architecture and antitumor surveillance processes and consequently enabling tumor growth and survival. While looking for cell-to-cell signaling mechanisms that are common to both brain development and cancer progression, we have studied the infiltration process in glioblastoma multiforme (GBM), which is the most malignant primary brain tumor and with the worst prognosis. Cell-to-cell contacts, by means of filopodia-like structures, between GBM cells and brain pericytes (PCs) are necessary for adequate cell signaling during cancer infiltration; similarly, contacts between embryonic regions, via cytonemes, are required for embryo regionalization and development. This GBM–PC interaction provokes two important changes in the physiological function of these perivascular cells, namely, (i) vascular co-option with changes in cell contractility and vascular malformation, and (ii) changes in the PC transcriptome, modifying the microvesicles and protein secretome, which leads to the development of an immunosuppressive phenotype that promotes tumor immune tolerance. Moreover, the GTPase Cdc42 regulates cell polarity across organisms, from yeast to humans, playing a central role in GBM cell–PC interaction and maintaining vascular co-option. As such, a review of the molecular and cellular mechanisms underlying the development and maintenance of the physical interactions between cancer cells and PCs is of particular interest.
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spelling pubmed-101775532023-05-13 Pericyte–Glioblastoma Cell Interaction: A Key Target to Prevent Glioblastoma Progression Pombero, Ana Garcia-Lopez, Raquel Martínez, Salvador Cells Review Multiple biological processes rely on direct intercellular interactions to regulate cell proliferation and migration in embryonic development and cancer processes. Tumor development and growth depends on close interactions between cancer cells and cells in the tumor microenvironment. During embryonic development, morphogenetic signals and direct cell contacts control cell proliferation, polarity, and morphogenesis. Cancer cells communicate with cells in the tumor niche through molecular signals and intercellular contacts, thereby modifying the vascular architecture and antitumor surveillance processes and consequently enabling tumor growth and survival. While looking for cell-to-cell signaling mechanisms that are common to both brain development and cancer progression, we have studied the infiltration process in glioblastoma multiforme (GBM), which is the most malignant primary brain tumor and with the worst prognosis. Cell-to-cell contacts, by means of filopodia-like structures, between GBM cells and brain pericytes (PCs) are necessary for adequate cell signaling during cancer infiltration; similarly, contacts between embryonic regions, via cytonemes, are required for embryo regionalization and development. This GBM–PC interaction provokes two important changes in the physiological function of these perivascular cells, namely, (i) vascular co-option with changes in cell contractility and vascular malformation, and (ii) changes in the PC transcriptome, modifying the microvesicles and protein secretome, which leads to the development of an immunosuppressive phenotype that promotes tumor immune tolerance. Moreover, the GTPase Cdc42 regulates cell polarity across organisms, from yeast to humans, playing a central role in GBM cell–PC interaction and maintaining vascular co-option. As such, a review of the molecular and cellular mechanisms underlying the development and maintenance of the physical interactions between cancer cells and PCs is of particular interest. MDPI 2023-05-05 /pmc/articles/PMC10177553/ /pubmed/37174724 http://dx.doi.org/10.3390/cells12091324 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pombero, Ana
Garcia-Lopez, Raquel
Martínez, Salvador
Pericyte–Glioblastoma Cell Interaction: A Key Target to Prevent Glioblastoma Progression
title Pericyte–Glioblastoma Cell Interaction: A Key Target to Prevent Glioblastoma Progression
title_full Pericyte–Glioblastoma Cell Interaction: A Key Target to Prevent Glioblastoma Progression
title_fullStr Pericyte–Glioblastoma Cell Interaction: A Key Target to Prevent Glioblastoma Progression
title_full_unstemmed Pericyte–Glioblastoma Cell Interaction: A Key Target to Prevent Glioblastoma Progression
title_short Pericyte–Glioblastoma Cell Interaction: A Key Target to Prevent Glioblastoma Progression
title_sort pericyte–glioblastoma cell interaction: a key target to prevent glioblastoma progression
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177553/
https://www.ncbi.nlm.nih.gov/pubmed/37174724
http://dx.doi.org/10.3390/cells12091324
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