Show pageBacklinksCite current pageExport to PDFBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. In a study, both [[U118]] cell and [[GSC23]] cell exhibited good printability and [[cell proliferation]]. Compared with 3D-U118, 3D-[[GSC]]23 had a greater ability to form cell [[spheroid]]s, to secrete [[VEGFA]], and to form tubule-like structures in vitro. More importantly, 3D-GSC23 cells had a greater power to transdifferentiate into functional [[endothelial cell]]s, and [[blood vessel]]s composed of [[tumor cell]]s with an abnormal endothelial phenotype was observed in vivo. In summary, 3D bioprinted [[hydrogel]] [[scaffold]] provided a suitable [[tumor microenvironment]] (TME) for glioma cells and GSCs. This bioprinted model supported a novel TME for the research of glioma cells, especially GSCs in glioma vascularization and therapeutic targeting of [[tumor angiogenesis]] ((Wang X, Li X, Ding J, et al. 3D bioprinted glioma microenvironment for glioma vascularization [published online ahead of print, 2020 Aug 10]. J Biomed Mater Res A. 2020;10.1002/jbm.a.37082. doi:10.1002/jbm.a.37082)). gsc23.txt Last modified: 2024/06/07 02:56by 127.0.0.1