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VEGFC negatively regulates the growth and aggressiveness of medulloblastoma cells

Medulloblastoma (MB), the most common brain pediatric tumor, is a pathology composed of four molecular subgroups. Despite a multimodal treatment, 30% of the patients eventually relapse, with the fatal appearance of metastases within 5 years. The major actors of metastatic dissemination are the lymph...

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Autores principales: Penco-Campillo, Manon, Comoglio, Yannick, Feliz Morel, Álvaro Javier, Hanna, Rita, Durivault, Jérôme, Leloire, Magalie, Mejias, Bastien, Pagnuzzi, Marina, Morot, Amandine, Burel-Vandenbos, Fanny, Selby, Matthew, Williamson, Daniel, Clifford, Steven C., Claren, Audrey, Doyen, Jérôme, Picco, Vincent, Martial, Sonia, Pagès, Gilles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568583/
https://www.ncbi.nlm.nih.gov/pubmed/33067561
http://dx.doi.org/10.1038/s42003-020-01306-4
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author Penco-Campillo, Manon
Comoglio, Yannick
Feliz Morel, Álvaro Javier
Hanna, Rita
Durivault, Jérôme
Leloire, Magalie
Mejias, Bastien
Pagnuzzi, Marina
Morot, Amandine
Burel-Vandenbos, Fanny
Selby, Matthew
Williamson, Daniel
Clifford, Steven C.
Claren, Audrey
Doyen, Jérôme
Picco, Vincent
Martial, Sonia
Pagès, Gilles
author_facet Penco-Campillo, Manon
Comoglio, Yannick
Feliz Morel, Álvaro Javier
Hanna, Rita
Durivault, Jérôme
Leloire, Magalie
Mejias, Bastien
Pagnuzzi, Marina
Morot, Amandine
Burel-Vandenbos, Fanny
Selby, Matthew
Williamson, Daniel
Clifford, Steven C.
Claren, Audrey
Doyen, Jérôme
Picco, Vincent
Martial, Sonia
Pagès, Gilles
author_sort Penco-Campillo, Manon
collection PubMed
description Medulloblastoma (MB), the most common brain pediatric tumor, is a pathology composed of four molecular subgroups. Despite a multimodal treatment, 30% of the patients eventually relapse, with the fatal appearance of metastases within 5 years. The major actors of metastatic dissemination are the lymphatic vessel growth factor, VEGFC, and its receptors/co-receptors. Here, we show that VEGFC is inversely correlated to cell aggressiveness. Indeed, VEGFC decreases MB cell proliferation and migration, and their ability to form pseudo-vessel in vitro. Irradiation resistant-cells, which present high levels of VEGFC, lose the ability to migrate and to form vessel-like structures. Thus, irradiation reduces MB cell aggressiveness via a VEGFC-dependent process. Cells intrinsically or ectopically overexpressing VEGFC and irradiation-resistant cells form smaller experimental tumors in nude mice. Opposite to the common dogma, our results give strong arguments in favor of VEGFC as a negative regulator of MB growth.
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spelling pubmed-75685832020-10-20 VEGFC negatively regulates the growth and aggressiveness of medulloblastoma cells Penco-Campillo, Manon Comoglio, Yannick Feliz Morel, Álvaro Javier Hanna, Rita Durivault, Jérôme Leloire, Magalie Mejias, Bastien Pagnuzzi, Marina Morot, Amandine Burel-Vandenbos, Fanny Selby, Matthew Williamson, Daniel Clifford, Steven C. Claren, Audrey Doyen, Jérôme Picco, Vincent Martial, Sonia Pagès, Gilles Commun Biol Article Medulloblastoma (MB), the most common brain pediatric tumor, is a pathology composed of four molecular subgroups. Despite a multimodal treatment, 30% of the patients eventually relapse, with the fatal appearance of metastases within 5 years. The major actors of metastatic dissemination are the lymphatic vessel growth factor, VEGFC, and its receptors/co-receptors. Here, we show that VEGFC is inversely correlated to cell aggressiveness. Indeed, VEGFC decreases MB cell proliferation and migration, and their ability to form pseudo-vessel in vitro. Irradiation resistant-cells, which present high levels of VEGFC, lose the ability to migrate and to form vessel-like structures. Thus, irradiation reduces MB cell aggressiveness via a VEGFC-dependent process. Cells intrinsically or ectopically overexpressing VEGFC and irradiation-resistant cells form smaller experimental tumors in nude mice. Opposite to the common dogma, our results give strong arguments in favor of VEGFC as a negative regulator of MB growth. Nature Publishing Group UK 2020-10-16 /pmc/articles/PMC7568583/ /pubmed/33067561 http://dx.doi.org/10.1038/s42003-020-01306-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Penco-Campillo, Manon
Comoglio, Yannick
Feliz Morel, Álvaro Javier
Hanna, Rita
Durivault, Jérôme
Leloire, Magalie
Mejias, Bastien
Pagnuzzi, Marina
Morot, Amandine
Burel-Vandenbos, Fanny
Selby, Matthew
Williamson, Daniel
Clifford, Steven C.
Claren, Audrey
Doyen, Jérôme
Picco, Vincent
Martial, Sonia
Pagès, Gilles
VEGFC negatively regulates the growth and aggressiveness of medulloblastoma cells
title VEGFC negatively regulates the growth and aggressiveness of medulloblastoma cells
title_full VEGFC negatively regulates the growth and aggressiveness of medulloblastoma cells
title_fullStr VEGFC negatively regulates the growth and aggressiveness of medulloblastoma cells
title_full_unstemmed VEGFC negatively regulates the growth and aggressiveness of medulloblastoma cells
title_short VEGFC negatively regulates the growth and aggressiveness of medulloblastoma cells
title_sort vegfc negatively regulates the growth and aggressiveness of medulloblastoma cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568583/
https://www.ncbi.nlm.nih.gov/pubmed/33067561
http://dx.doi.org/10.1038/s42003-020-01306-4
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