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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[31]  
Alitalo K(2017)The whole-genome landscape of medulloblastoma subtypes Nature 547 67315-167.
[32]  
Duong T(2017)The role of prospero homeobox 1 (PROX1) expression in follicular thyroid carcinoma cells Oncotarget 8 739-675.
[33]  
Koopman P(2017)Human CAFs promote lymphangiogenesis in ovarian cancer via the Hh-VEGF-C signaling axis Oncotarget 8 155-2072.
[34]  
Francois M(2015)Cellular fibronectin 1 promotes VEGF-C expression, lymphangiogenesis and lymph node metastasis associated with human oral squamous cell carcinoma Clin. Exp. Metastasis 32 661-2513.
[35]  
Cavalli FMG(2014)Hypoxia induces VEGF-C expression in metastatic tumor cells via a HIF-1α-independent translation-mediated mechanism Cell Rep. 6 2064-1769
[36]  
Prud’homme GJ(2019)VEGFC acts as a double-edged sword in renal cell carcinoma aggressiveness Theranostics 9 2501-45
[37]  
Glinka Y(2001)Angiogenic profile of childhood primitive neuroectodermal brain tumours/medulloblastomas Eur. J. Cancer 37 1761-25
[38]  
Favier B(2017)Notch1 promotes vasculogenic mimicry in hepatocellular carcinoma by inducing EMT signaling Oncotarget 8 21-1631.
[39]  
Caunt M(2016)The relationship between vasculogenic mimicry and epithelial-mesenchymal transitions J. Cell Mol. Med. 20 10-8670
[40]  
Wang J(2016)EMT: 2016 Cell 166 1626-249