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Impact of adjustable cryogel properties on the performance of prostate cancer cells in 3D
BACKGROUND: Biochemical and physical characteristics of extracellular environment play a key role in assisting cell behavior over different molecular pathways. In this study, we investigated how the presence of chemical binding sites, the pore network and the stiffness of designed scaffolds affected...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923005/ https://www.ncbi.nlm.nih.gov/pubmed/27386348 http://dx.doi.org/10.1186/s40064-016-2629-z |
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author | Bäcker, A. Göppert, B. Sturm, S. Abaffy, P. Sollich, T. Gruhl, F. J. |
author_facet | Bäcker, A. Göppert, B. Sturm, S. Abaffy, P. Sollich, T. Gruhl, F. J. |
author_sort | Bäcker, A. |
collection | PubMed |
description | BACKGROUND: Biochemical and physical characteristics of extracellular environment play a key role in assisting cell behavior over different molecular pathways. In this study, we investigated how the presence of chemical binding sites, the pore network and the stiffness of designed scaffolds affected prostate cancer cells. METHODS: A blend of poly hydroxyethyl methacrylate–alginate–gelatin scaffold was synthesized by cryogelation process using polyethyleneglycol diacrylate (PEGda) and glutaraldehyde as cross linkers. The chemical and mechanical scaffold properties were varied by concentration of gelatin and PEGda, respectively. The pore network was modified by applying different ‘freezing time’. Growth, spheroid formation and localization of androgen receptor (AR) were measured to evaluate cell response within various cryogel types. RESULTS: Insufficient porosity in combination with a brittle nature affects cell growth negatively. Spheroid size was reduced by porosity, elasticity as well as by the absence of the cell adhesive motif composed of arginine, glycine und aspartic acid (RGD). Localization of AR indicates its activity and should be under normal culture conditions in the nucleus. But in this study, we could investigate for the first time that AR remains in the cytoplasm when AR positive prostate cancer cells are cultured in scaffolds without RGD as well as in case of an insufficient pore network (total porosity under 10 %) and a too less stiffness of around 10 kPa. CONCLUSIONS: The results indicate that for getting a reliable preclinical drug screening a three-dimensional prostate model system with appropriate biochemical and physical surrounding is needed. |
format | Online Article Text |
id | pubmed-4923005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-49230052016-07-06 Impact of adjustable cryogel properties on the performance of prostate cancer cells in 3D Bäcker, A. Göppert, B. Sturm, S. Abaffy, P. Sollich, T. Gruhl, F. J. Springerplus Research BACKGROUND: Biochemical and physical characteristics of extracellular environment play a key role in assisting cell behavior over different molecular pathways. In this study, we investigated how the presence of chemical binding sites, the pore network and the stiffness of designed scaffolds affected prostate cancer cells. METHODS: A blend of poly hydroxyethyl methacrylate–alginate–gelatin scaffold was synthesized by cryogelation process using polyethyleneglycol diacrylate (PEGda) and glutaraldehyde as cross linkers. The chemical and mechanical scaffold properties were varied by concentration of gelatin and PEGda, respectively. The pore network was modified by applying different ‘freezing time’. Growth, spheroid formation and localization of androgen receptor (AR) were measured to evaluate cell response within various cryogel types. RESULTS: Insufficient porosity in combination with a brittle nature affects cell growth negatively. Spheroid size was reduced by porosity, elasticity as well as by the absence of the cell adhesive motif composed of arginine, glycine und aspartic acid (RGD). Localization of AR indicates its activity and should be under normal culture conditions in the nucleus. But in this study, we could investigate for the first time that AR remains in the cytoplasm when AR positive prostate cancer cells are cultured in scaffolds without RGD as well as in case of an insufficient pore network (total porosity under 10 %) and a too less stiffness of around 10 kPa. CONCLUSIONS: The results indicate that for getting a reliable preclinical drug screening a three-dimensional prostate model system with appropriate biochemical and physical surrounding is needed. Springer International Publishing 2016-06-27 /pmc/articles/PMC4923005/ /pubmed/27386348 http://dx.doi.org/10.1186/s40064-016-2629-z Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Bäcker, A. Göppert, B. Sturm, S. Abaffy, P. Sollich, T. Gruhl, F. J. Impact of adjustable cryogel properties on the performance of prostate cancer cells in 3D |
title | Impact of adjustable cryogel properties on the performance of prostate cancer cells in 3D |
title_full | Impact of adjustable cryogel properties on the performance of prostate cancer cells in 3D |
title_fullStr | Impact of adjustable cryogel properties on the performance of prostate cancer cells in 3D |
title_full_unstemmed | Impact of adjustable cryogel properties on the performance of prostate cancer cells in 3D |
title_short | Impact of adjustable cryogel properties on the performance of prostate cancer cells in 3D |
title_sort | impact of adjustable cryogel properties on the performance of prostate cancer cells in 3d |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923005/ https://www.ncbi.nlm.nih.gov/pubmed/27386348 http://dx.doi.org/10.1186/s40064-016-2629-z |
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