| Literature DB >> 24075410 |
Stephen J Florczyk1, Kui Wang1, Soumen Jana1, David L Wood1, Samara K Sytsma1, Jonathan Sham2, Forrest M Kievit1,3, Miqin Zhang1,3.
Abstract
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-1α 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.Entities:
Keywords: Cancer stem cell; Glioma; Invasion; Multidrug resistance; Spheroid
Mesh:
Substances:
Year: 2013 PMID: 24075410 PMCID: PMC3843957 DOI: 10.1016/j.biomaterials.2013.09.034
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479