生物
胶质瘤
利基
干细胞
人口
转铁蛋白
癌症干细胞
细胞生物学
细胞培养
癌症研究
生物化学
遗传学
人口学
社会学
作者
Kouichi Tabu,Nozomi Muramatsu,Christian Mangani,Mei Wu,Rong Zhang,Taichi Kimura,Kazuo Terashima,Norihisa Bizen,Ryosuke Kimura,Wenqian Wang,Yoshitaka Murota,Yasuhiro Kokubu,Ikuo Nobuhisa,Tetsushi Kagawa,Issay Kitabayashi,Mark Bradley,Tetsuya Taga
出处
期刊:Stem Cells
[Wiley]
日期:2016-01-29
卷期号:34 (5): 1151-1162
被引量:22
摘要
Cancer stem cells (CSCs) are believed to be maintained within a microenvironmental niche. Here we used polymer microarrays for the rapid and efficient identification of glioma CSC (GSC) niche mimicries and identified a urethane-based synthetic polymer, upon which two groups of niche components, namely extracellular matrices (ECMs) and iron are revealed. In cultures, side population (SP) cells, defined as GSCs in the rat C6 glioma cell line, are more efficiently sustained in the presence of their differentiated progenies expressing higher levels of ECMs and transferrin, while in xenografts, ECMs are supplied by the vascular endothelial cells (VECs), including SP cell-derived ones with distinctively greater ability to retain xenobiotics than host VECs. Iron is stored in tumor infiltrating host macrophages (Mφs), whose protumoral activity is potently enhanced by SP cell-secreted soluble factor(s). Finally, coexpression of ECM-, iron-, and Mφ-related genes is found to be predictive of glioma patients' outcome. Our polymer-based approach reveals the intrinsic capacities of GSCs, to adapt the environment to organize a self-advantageous microenvironment niche, for their maintenance and expansion, which redefines the current concept of anti-CSC niche therapy and has the potential to accelerate cancer therapy development. Stem Cells 2016;34:1151-1162.
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