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Comparison of Tumor- and Bone Marrow-Derived Mesenchymal Stromal/Stem Cells from Patients with High-Grade Osteosarcoma

Osteosarcoma (OS) is suspected to originate from dysfunctional mesenchymal stromal/stem cells (MSC). We sought to identify OS-derived cells (OSDC) with potential cancer stem cell (CSC) properties by comparing OSDC to MSC derived from bone marrow of patients. This study included in vitro characteriza...

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Autores principales: Le Nail, Louis-Romée, Brennan, Meadhbh, Rosset, Philippe, Deschaseaux, Frédéric, Piloquet, Philippe, Pichon, Olivier, Le Caignec, Cédric, Crenn, Vincent, Layrolle, Pierre, Hérault, Olivier, De Pinieux, Gonzague, Trichet, Valérie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5877568/
https://www.ncbi.nlm.nih.gov/pubmed/29494553
http://dx.doi.org/10.3390/ijms19030707
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author Le Nail, Louis-Romée
Brennan, Meadhbh
Rosset, Philippe
Deschaseaux, Frédéric
Piloquet, Philippe
Pichon, Olivier
Le Caignec, Cédric
Crenn, Vincent
Layrolle, Pierre
Hérault, Olivier
De Pinieux, Gonzague
Trichet, Valérie
author_facet Le Nail, Louis-Romée
Brennan, Meadhbh
Rosset, Philippe
Deschaseaux, Frédéric
Piloquet, Philippe
Pichon, Olivier
Le Caignec, Cédric
Crenn, Vincent
Layrolle, Pierre
Hérault, Olivier
De Pinieux, Gonzague
Trichet, Valérie
author_sort Le Nail, Louis-Romée
collection PubMed
description Osteosarcoma (OS) is suspected to originate from dysfunctional mesenchymal stromal/stem cells (MSC). We sought to identify OS-derived cells (OSDC) with potential cancer stem cell (CSC) properties by comparing OSDC to MSC derived from bone marrow of patients. This study included in vitro characterization with sphere forming assays, differentiation assays, cytogenetic analysis, and in vivo investigations of their tumorigenicity and tumor supportive capacities. Primary cell lines were isolated from nine high-grade OS samples. All primary cell lines demonstrated stromal cell characteristics. Compared to MSC, OSDC presented a higher ability to form sphere clones, indicating a potential CSC phenotype, and were more efficient at differentiation towards osteoblasts. None of the OSDC displayed the complex chromosome rearrangements typical of high grade OS and none of them induced tumors in immunodeficient mice. However, two OSDC demonstrated focused genomic abnormalities. Three out of seven, and six out of seven OSDC showed a supportive role on local tumor development, and on metastatic progression to the lungs, respectively, when co-injected with OS cells in nude mice. The observation of OS-associated stromal cells with rare genetic abnormalities and with the capacity to sustain tumor progression may have implications for future tumor treatments.
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spelling pubmed-58775682018-04-09 Comparison of Tumor- and Bone Marrow-Derived Mesenchymal Stromal/Stem Cells from Patients with High-Grade Osteosarcoma Le Nail, Louis-Romée Brennan, Meadhbh Rosset, Philippe Deschaseaux, Frédéric Piloquet, Philippe Pichon, Olivier Le Caignec, Cédric Crenn, Vincent Layrolle, Pierre Hérault, Olivier De Pinieux, Gonzague Trichet, Valérie Int J Mol Sci Article Osteosarcoma (OS) is suspected to originate from dysfunctional mesenchymal stromal/stem cells (MSC). We sought to identify OS-derived cells (OSDC) with potential cancer stem cell (CSC) properties by comparing OSDC to MSC derived from bone marrow of patients. This study included in vitro characterization with sphere forming assays, differentiation assays, cytogenetic analysis, and in vivo investigations of their tumorigenicity and tumor supportive capacities. Primary cell lines were isolated from nine high-grade OS samples. All primary cell lines demonstrated stromal cell characteristics. Compared to MSC, OSDC presented a higher ability to form sphere clones, indicating a potential CSC phenotype, and were more efficient at differentiation towards osteoblasts. None of the OSDC displayed the complex chromosome rearrangements typical of high grade OS and none of them induced tumors in immunodeficient mice. However, two OSDC demonstrated focused genomic abnormalities. Three out of seven, and six out of seven OSDC showed a supportive role on local tumor development, and on metastatic progression to the lungs, respectively, when co-injected with OS cells in nude mice. The observation of OS-associated stromal cells with rare genetic abnormalities and with the capacity to sustain tumor progression may have implications for future tumor treatments. MDPI 2018-03-01 /pmc/articles/PMC5877568/ /pubmed/29494553 http://dx.doi.org/10.3390/ijms19030707 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Le Nail, Louis-Romée
Brennan, Meadhbh
Rosset, Philippe
Deschaseaux, Frédéric
Piloquet, Philippe
Pichon, Olivier
Le Caignec, Cédric
Crenn, Vincent
Layrolle, Pierre
Hérault, Olivier
De Pinieux, Gonzague
Trichet, Valérie
Comparison of Tumor- and Bone Marrow-Derived Mesenchymal Stromal/Stem Cells from Patients with High-Grade Osteosarcoma
title Comparison of Tumor- and Bone Marrow-Derived Mesenchymal Stromal/Stem Cells from Patients with High-Grade Osteosarcoma
title_full Comparison of Tumor- and Bone Marrow-Derived Mesenchymal Stromal/Stem Cells from Patients with High-Grade Osteosarcoma
title_fullStr Comparison of Tumor- and Bone Marrow-Derived Mesenchymal Stromal/Stem Cells from Patients with High-Grade Osteosarcoma
title_full_unstemmed Comparison of Tumor- and Bone Marrow-Derived Mesenchymal Stromal/Stem Cells from Patients with High-Grade Osteosarcoma
title_short Comparison of Tumor- and Bone Marrow-Derived Mesenchymal Stromal/Stem Cells from Patients with High-Grade Osteosarcoma
title_sort comparison of tumor- and bone marrow-derived mesenchymal stromal/stem cells from patients with high-grade osteosarcoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5877568/
https://www.ncbi.nlm.nih.gov/pubmed/29494553
http://dx.doi.org/10.3390/ijms19030707
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