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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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Detalles Bibliográficos
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
Descripción
Sumario: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.