| Literature DB >> 26822103 |
Kouichi Tabu1, Nozomi Muramatsu1, Christian Mangani2, Mei Wu2, Rong Zhang2,3, Taichi Kimura4, Kazuo Terashima1, Norihisa Bizen1, Ryosuke Kimura1, Wenqian Wang1, Yoshitaka Murota1, Yasuhiro Kokubu1, Ikuo Nobuhisa1, Tetsushi Kagawa1, Issay Kitabayashi5, Mark Bradley2, Tetsuya Taga1.
Abstract
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.Entities:
Keywords: Cancer stem cells; Extracellular matrix; Glioma; Macrophages; Polymers; Stem cell niche
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Year: 2016 PMID: 26822103 DOI: 10.1002/stem.2299
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277