| Literature DB >> 31279100 |
Kailei Xu1, Kavya Ganapathy2, Thomas Andl2, Zi Wang1, John A Copland3, Ratna Chakrabarti2, Stephen J Florczyk4.
Abstract
Prostate cancer (PCa) is a leading cause of death for men worldwide. Most PCa patients die from metastasis and bone is the most common metastatic site. Three dimensional (3D) porous chitosan-alginate (CA) scaffolds were developed for bone tissue engineering and demonstrated for culture of cancer cells and enrichment of cancer stem cells. However, only a single scaffold composition was studied. Three compositions of 3D porous CA scaffolds (2, 4, and 6 wt%) were used to investigate the effect of scaffold stiffness on PCa cell response with PC-3, C4-2B, and 22Rv1 cell lines. The PC-3 cells formed cell clusters while the C4-2B and 22Rv1 cells formed multicellular spheroids. The three cell lines demonstrated stiffness independent cell growth and expressed phenotypic PCa biomarkers. The osteoblastic PCa lines C4-2B and 22Rv1 mineralized in basal media, while the osteolytic PC-3 line did not, demonstrating that CA scaffold cultures revealed differences in PCa phenotypes. The CA scaffolds are a 3D culture platform that supports PCa growth and phenotypic expression with adjustable scaffold stiffness to mimic stages of metastatic progression. Further investigation of the scaffolds for co-culture of PCa cells with fibroblasts and primary PCa cell culture should be conducted to develop a platform for screening chemotherapies.Entities:
Keywords: Mechanotransduction; Mineralization; Polyelectrolyte complex; Prostate cancer; Tumor microenvironment; Tumor model
Year: 2019 PMID: 31279100 DOI: 10.1016/j.biomaterials.2019.119311
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479