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PMID: 31279100 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

3D porous chitosan-alginate scaffold stiffness promotes differential responses in prostate cancer cell lines.

Biomaterials ·Vol. 217 ·2019-00-00 ·Pages 119311

Xu K, Ganapathy K, Andl T, Wang Z, Copland JA, Chakrabarti R, Florczyk SJ

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.

Keywords
Mechanotransduction Mineralization Polyelectrolyte complex Prostate cancer Tumor microenvironment Tumor model
MeSH Terms
Actins/metabolism Alginates/chemistry Cadherins/metabolism Calcification, Physiologic Cell Communication Cell Line, Tumor Cell Proliferation Cell Shape Chitosan/chemistry Gene Expression Regulation, Neoplastic Humans Male Neoplasm Proteins/genetics,metabolism Osteoblasts/metabolism Osteocalcin/metabolism Phenotype Porosity Prostatic Neoplasms/genetics,pathology,ultrastructure Tissue Scaffolds/chemistry
Chemicals
Actins Alginates Cadherins Neoplasm Proteins Osteocalcin Chitosan
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Xu Kailei
Department of Materials Science and Engineering, University of Central Florida, Orlando, FL, 32816-2455, USA.
Ganapathy Kavya
Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL, 32827, USA.
Andl Thomas
Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL, 32827, USA.
Wang Zi
Department of Materials Science and Engineering, University of Central Florida, Orlando, FL, 32816-2455, USA.
Copland John A
Department of Cancer Biology, Mayo Clinic, Jacksonville, FL, 32224, USA.
Chakrabarti Ratna
Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL, 32827, USA.
Florczyk Stephen J
Department of Materials Science and Engineering, University of Central Florida, Orlando, FL, 32816-2455, USA; Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL, 32827, USA. Electronic address: stephen.florczyk@ucf.edu.
Article Info
Journal
Biomaterials
Abbr.
Biomaterials
ISSN
1878-5905
Published
2019-00-00
Epub
2019-00-28
Pages
119311
Language
English
Region
Netherlands
NLM ID
8100316
Subset
IM
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