VEGFC negatively regulates the growth and aggressiveness of medulloblastoma cells

被引:0
作者
Manon Penco-Campillo
Yannick Comoglio
Álvaro Javier Feliz Morel
Rita Hanna
Jérôme Durivault
Magalie Leloire
Bastien Mejias
Marina Pagnuzzi
Amandine Morot
Fanny Burel-Vandenbos
Matthew Selby
Daniel Williamson
Steven C. Clifford
Audrey Claren
Jérôme Doyen
Vincent Picco
Sonia Martial
Gilles Pagès
机构
[1] Université Côte d’Azur,
[2] Institute for Research on Cancer and Ageing of Nice (IRCAN),undefined
[3] CNRS UMR7284,undefined
[4] INSERM U1081,undefined
[5] Fédération Claude Lalanne (FCL),undefined
[6] Biomedical Department,undefined
[7] Centre Scientifique de Monaco (CSM),undefined
[8] Anatomo-pathology Department,undefined
[9] Nice University Hospital,undefined
[10] Wolfson Childhood Cancer Research Centre,undefined
[11] Newcastle University,undefined
[12] Centre Antoine Lacassagne Cancer Institute,undefined
来源
Communications Biology | / 3卷
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摘要
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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