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Scaffold-based 3D cellular models mimicking the heterogeneity of osteosarcoma stem cell niche

The failure of the osteosarcoma conventional therapies leads to the growing need for novel therapeutic strategies. The lack of specificity for the Cancer Stem Cells (CSCs) population has been recently identified as the main limitation in the current therapies. Moreover, the traditional two-dimension...

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Autores principales: Bassi, Giada, Panseri, Silvia, Dozio, Samuele Maria, Sandri, Monica, Campodoni, Elisabetta, Dapporto, Massimiliano, Sprio, Simone, Tampieri, Anna, Montesi, Monica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749131/
https://www.ncbi.nlm.nih.gov/pubmed/33339857
http://dx.doi.org/10.1038/s41598-020-79448-y
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author Bassi, Giada
Panseri, Silvia
Dozio, Samuele Maria
Sandri, Monica
Campodoni, Elisabetta
Dapporto, Massimiliano
Sprio, Simone
Tampieri, Anna
Montesi, Monica
author_facet Bassi, Giada
Panseri, Silvia
Dozio, Samuele Maria
Sandri, Monica
Campodoni, Elisabetta
Dapporto, Massimiliano
Sprio, Simone
Tampieri, Anna
Montesi, Monica
author_sort Bassi, Giada
collection PubMed
description The failure of the osteosarcoma conventional therapies leads to the growing need for novel therapeutic strategies. The lack of specificity for the Cancer Stem Cells (CSCs) population has been recently identified as the main limitation in the current therapies. Moreover, the traditional two-dimensional (2D) in vitro models, employed in the drug testing and screening as well as in the study of cell and molecular biology, are affected by a poor in vitro-in vivo translation ability. To overcome these limitations, this work provides two tumour engineering approaches as new tools to address osteosarcoma and improve therapy outcomes. In detail, two different hydroxyapatite-based bone-mimicking scaffolds were used to recapitulate aspects of the in vivo tumour microenvironment, focusing on CSCs niche. The biological performance of human osteosarcoma cell lines (MG63 and SAOS-2) and enriched-CSCs were deeply analysed in these complex cell culture models. The results highlight the fundamental role of the tumour microenvironment proving the mimicry of osteosarcoma stem cell niche by the use of CSCs together with the biomimetic scaffolds, compared to conventional 2D culture systems. These advanced 3D cell culture in vitro tumour models could improve the predictivity of preclinical studies and strongly enhance the clinical translation.
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spelling pubmed-77491312020-12-22 Scaffold-based 3D cellular models mimicking the heterogeneity of osteosarcoma stem cell niche Bassi, Giada Panseri, Silvia Dozio, Samuele Maria Sandri, Monica Campodoni, Elisabetta Dapporto, Massimiliano Sprio, Simone Tampieri, Anna Montesi, Monica Sci Rep Article The failure of the osteosarcoma conventional therapies leads to the growing need for novel therapeutic strategies. The lack of specificity for the Cancer Stem Cells (CSCs) population has been recently identified as the main limitation in the current therapies. Moreover, the traditional two-dimensional (2D) in vitro models, employed in the drug testing and screening as well as in the study of cell and molecular biology, are affected by a poor in vitro-in vivo translation ability. To overcome these limitations, this work provides two tumour engineering approaches as new tools to address osteosarcoma and improve therapy outcomes. In detail, two different hydroxyapatite-based bone-mimicking scaffolds were used to recapitulate aspects of the in vivo tumour microenvironment, focusing on CSCs niche. The biological performance of human osteosarcoma cell lines (MG63 and SAOS-2) and enriched-CSCs were deeply analysed in these complex cell culture models. The results highlight the fundamental role of the tumour microenvironment proving the mimicry of osteosarcoma stem cell niche by the use of CSCs together with the biomimetic scaffolds, compared to conventional 2D culture systems. These advanced 3D cell culture in vitro tumour models could improve the predictivity of preclinical studies and strongly enhance the clinical translation. Nature Publishing Group UK 2020-12-18 /pmc/articles/PMC7749131/ /pubmed/33339857 http://dx.doi.org/10.1038/s41598-020-79448-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bassi, Giada
Panseri, Silvia
Dozio, Samuele Maria
Sandri, Monica
Campodoni, Elisabetta
Dapporto, Massimiliano
Sprio, Simone
Tampieri, Anna
Montesi, Monica
Scaffold-based 3D cellular models mimicking the heterogeneity of osteosarcoma stem cell niche
title Scaffold-based 3D cellular models mimicking the heterogeneity of osteosarcoma stem cell niche
title_full Scaffold-based 3D cellular models mimicking the heterogeneity of osteosarcoma stem cell niche
title_fullStr Scaffold-based 3D cellular models mimicking the heterogeneity of osteosarcoma stem cell niche
title_full_unstemmed Scaffold-based 3D cellular models mimicking the heterogeneity of osteosarcoma stem cell niche
title_short Scaffold-based 3D cellular models mimicking the heterogeneity of osteosarcoma stem cell niche
title_sort scaffold-based 3d cellular models mimicking the heterogeneity of osteosarcoma stem cell niche
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749131/
https://www.ncbi.nlm.nih.gov/pubmed/33339857
http://dx.doi.org/10.1038/s41598-020-79448-y
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