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Development of extracellular matrix supported 3D culture of renal cancer cells and renal cancer stem cells
Novel experimental conditions of cancer cell line culture have evolved throughout the recent years, with significantly growing interest in xeno-free, serum-free and three-dimensional culture variants. The choice of proper culture media may enable to mimic tumor microenvironment and promotion of canc...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368519/ https://www.ncbi.nlm.nih.gov/pubmed/30599072 http://dx.doi.org/10.1007/s10616-018-0273-x |
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author | Maliszewska-Olejniczak, Kamila Brodaczewska, Klaudia K. Bielecka, Zofia F. Solarek, Wojciech Kornakiewicz, Anna Szczylik, Cezary Porta, Camillo Czarnecka, Anna M. |
author_facet | Maliszewska-Olejniczak, Kamila Brodaczewska, Klaudia K. Bielecka, Zofia F. Solarek, Wojciech Kornakiewicz, Anna Szczylik, Cezary Porta, Camillo Czarnecka, Anna M. |
author_sort | Maliszewska-Olejniczak, Kamila |
collection | PubMed |
description | Novel experimental conditions of cancer cell line culture have evolved throughout the recent years, with significantly growing interest in xeno-free, serum-free and three-dimensional culture variants. The choice of proper culture media may enable to mimic tumor microenvironment and promotion of cancer stem cells proliferation. To assess whether stem-like phenotype inducing media may be applied in renal cancer stem cell research, we performed a widespread screening of 13 cell culture media dedicated for mesenchymal cells, stem cells as well as mesenchymal stem cells. We have also screened extracellular matrix compounds and selected optimal RCC 3D—ECM supported culture model. Our results revealed that 786-O as well as HKCSCs cell line cultures in xeno-free media (NutriStem/StemXvivo) and laminin coated plates provide a useful tool in RCC cancer biology research and at the same time enable effective drug toxicity screening. We propose bio-mimic 3D RCC cell culture model with specific low-serum and xeno-free media that promote RCC cell viability and stem-like phenotype according to the tested genes encoding stemness factors including E-cadherin, N-cadherin, HIF1, HIF2, VEGF, SOX2, PAX2 and NESTIN. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10616-018-0273-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6368519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-63685192019-02-27 Development of extracellular matrix supported 3D culture of renal cancer cells and renal cancer stem cells Maliszewska-Olejniczak, Kamila Brodaczewska, Klaudia K. Bielecka, Zofia F. Solarek, Wojciech Kornakiewicz, Anna Szczylik, Cezary Porta, Camillo Czarnecka, Anna M. Cytotechnology Article Novel experimental conditions of cancer cell line culture have evolved throughout the recent years, with significantly growing interest in xeno-free, serum-free and three-dimensional culture variants. The choice of proper culture media may enable to mimic tumor microenvironment and promotion of cancer stem cells proliferation. To assess whether stem-like phenotype inducing media may be applied in renal cancer stem cell research, we performed a widespread screening of 13 cell culture media dedicated for mesenchymal cells, stem cells as well as mesenchymal stem cells. We have also screened extracellular matrix compounds and selected optimal RCC 3D—ECM supported culture model. Our results revealed that 786-O as well as HKCSCs cell line cultures in xeno-free media (NutriStem/StemXvivo) and laminin coated plates provide a useful tool in RCC cancer biology research and at the same time enable effective drug toxicity screening. We propose bio-mimic 3D RCC cell culture model with specific low-serum and xeno-free media that promote RCC cell viability and stem-like phenotype according to the tested genes encoding stemness factors including E-cadherin, N-cadherin, HIF1, HIF2, VEGF, SOX2, PAX2 and NESTIN. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10616-018-0273-x) contains supplementary material, which is available to authorized users. Springer Netherlands 2018-12-31 2019-02 /pmc/articles/PMC6368519/ /pubmed/30599072 http://dx.doi.org/10.1007/s10616-018-0273-x Text en © The Author(s) 2018 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 | Article Maliszewska-Olejniczak, Kamila Brodaczewska, Klaudia K. Bielecka, Zofia F. Solarek, Wojciech Kornakiewicz, Anna Szczylik, Cezary Porta, Camillo Czarnecka, Anna M. Development of extracellular matrix supported 3D culture of renal cancer cells and renal cancer stem cells |
title | Development of extracellular matrix supported 3D culture of renal cancer cells and renal cancer stem cells |
title_full | Development of extracellular matrix supported 3D culture of renal cancer cells and renal cancer stem cells |
title_fullStr | Development of extracellular matrix supported 3D culture of renal cancer cells and renal cancer stem cells |
title_full_unstemmed | Development of extracellular matrix supported 3D culture of renal cancer cells and renal cancer stem cells |
title_short | Development of extracellular matrix supported 3D culture of renal cancer cells and renal cancer stem cells |
title_sort | development of extracellular matrix supported 3d culture of renal cancer cells and renal cancer stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368519/ https://www.ncbi.nlm.nih.gov/pubmed/30599072 http://dx.doi.org/10.1007/s10616-018-0273-x |
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