Porous chitosan-hyaluronic acid scaffolds as a mimic of glioblastoma microenvironment ECM

被引:190
作者
Florczyk, Stephen J. [1 ]
Wang, Kui [1 ]
Jana, Soumen [1 ]
Wood, David L. [1 ]
Sytsma, Samara K. [1 ]
Sham, Jonathan G. [2 ]
Kievit, Forrest M. [1 ,3 ]
Zhang, Miqin [1 ,3 ]
机构
[1] Univ Washington, Dept Mat Sci & Engn, Seattle, WA 98195 USA
[2] Univ Washington, Dept Surg, Seattle, WA 98195 USA
[3] Univ Washington, Dept Neurol Surg, Seattle, WA 98195 USA
关键词
Spheroid; Cancer stem cell; Multidrug resistance; Invasion; Glioma; GLIOMA STEM-CELLS; 3D CULTURE; MULTIDRUG-RESISTANCE; CANCER-RESEARCH; BRAIN-TUMORS; IN-VITRO; HYPOXIA; MATRIX; EXPRESSION; POPULATION;
D O I
10.1016/j.biomaterials.2013.09.034
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cancer therapeutics are developed through extensive screening; however, many therapeutics evaluated with 2D in vitro cultures during pre-clinical trials suffer from lower efficacy in patients. Replicating the in vivo tumor microenvironment in vitro with three-dimensional (3D) porous scaffolds offers the possibility of generating more predictive pre-clinical models to enhance cancer treatment efficacy. We developed a chitosan and hyaluronic acid (HA) polyelectrolyte complex 3D porous scaffold and evaluated its physical properties. Chitosan-HA (C-HA) scaffolds had a highly porous network. C-HA scaffolds were compared to 2D surfaces for in vitro culture of U-118 MG human glioblastoma (GBM) cells. C-HA scaffold cultures promoted tumor spheroid formation and increased stem-like properties of GBM cells as evidenced by the upregulation of CD44, Nestin, Musashi-1, GFAP, and HIF-1 alpha as compared with 2D cultures. Additionally, the invasiveness of GBM cells cultured in C-HA scaffolds was significantly enhanced compared to those grown in 2D cultures. C-HA scaffold cultures were also more resistant to chemotherapy drugs, which corresponded to the increased expression of ABCG2 drug efflux transporter. These findings suggest that C-HA scaffolds offer promise as an in vitro GBM platform for study and screening of novel cancer therapeutics. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:10143 / 10150
页数:8
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