Fiche publication
Date publication
novembre 2017
Journal
Experimental cell research
Auteurs
Membres identifiés du Cancéropôle Est :
Dr BENKIRANE-JESSEL Nadia
,
Dr IDOUX-GILLET Ysia
,
Pr UBEAUD-SEQUIER Genevieve
,
Dr FUHRMANN Guy
Tous les auteurs :
Chaddad H, Kuchler-Bopp S, Fuhrmann G, Gegout H, Ubeaud-Sequier G, Schwinté P, Bornert F, Benkirane-Jessel N, Idoux-Gillet Y
Lien Pubmed
Résumé
Angiogenesis is now well known for being involved in tumor progression, aggressiveness, emergence of metastases, and also resistance to cancer therapies. In this study, to better mimic tumor angiogenesis encountered in vivo, we used 3D culture of osteosarcoma cells (MG-63) that we deposited on 2D endothelial cells (HUVEC) grown in monolayer. We report that endothelial cells combined with tumor cells were able to form a well-organized network, and that tubule-like structures corresponding to new vessels infiltrate tumor spheroids. These vessels presented a lumen and expressed specific markers as CD31 and collagen IV. The combination of 2D endothelial cells and 3D microtissues of tumor cells also increased expression of angiogenic factors as VEGF, CXCR4 and ICAM1. The cell environment is the key point to develop tumor vascularization in vitro and to be closer to tumor encountered in vivo.
Mots clés
Bone Neoplasms, blood supply, Cell Culture Techniques, methods, Cells, Cultured, Gene Expression Regulation, Neoplastic, Human Umbilical Vein Endothelial Cells, cytology, Humans, Neovascularization, Pathologic, genetics, Osteosarcoma, blood supply, Tissue Scaffolds, chemistry
Référence
Exp. Cell Res.. 2017 11 15;360(2):138-145
