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Comparison of Osteosarcoma Aggregated Tumour Models with Human Tissue by Multimodal Mass Spectrometry Imaging

Osteosarcoma (OS) is the most common primary bone malignancy and largely effects adolescents and young adults, with 60% of patients under the age of 25. There are multiple cell models of OS described in vitro that express the specific genetic alterations of the sarcoma. In the work reported here, mu...

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Autores principales: Flint, Lucy E., Hamm, Gregory, Ready, Joseph D., Ling, Stephanie, Duckett, Catherine J., Cross, Neil A., Cole, Laura M., Smith, David P., Goodwin, Richard J. A., Clench, Malcolm R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8401535/
https://www.ncbi.nlm.nih.gov/pubmed/34436447
http://dx.doi.org/10.3390/metabo11080506
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author Flint, Lucy E.
Hamm, Gregory
Ready, Joseph D.
Ling, Stephanie
Duckett, Catherine J.
Cross, Neil A.
Cole, Laura M.
Smith, David P.
Goodwin, Richard J. A.
Clench, Malcolm R.
author_facet Flint, Lucy E.
Hamm, Gregory
Ready, Joseph D.
Ling, Stephanie
Duckett, Catherine J.
Cross, Neil A.
Cole, Laura M.
Smith, David P.
Goodwin, Richard J. A.
Clench, Malcolm R.
author_sort Flint, Lucy E.
collection PubMed
description Osteosarcoma (OS) is the most common primary bone malignancy and largely effects adolescents and young adults, with 60% of patients under the age of 25. There are multiple cell models of OS described in vitro that express the specific genetic alterations of the sarcoma. In the work reported here, multiple mass spectrometry imaging (MSI) modalities were employed to characterise two aggregated cellular models of OS models formed using the MG63 and SAOS-2 cell lines. Phenotyping of the metabolite activity within the two OS aggregoid models was achieved and a comparison of the metabolite data with OS human tissue samples revealed relevant fatty acid and phospholipid markers. Although, annotations of these species require MS/MS analysis for confident identification of the metabolites. From the putative assignments however, it was suggested that the MG63 aggregoids are an aggressive tumour model that exhibited metastatic-like potential. Alternatively, the SAOS-2 aggregoids are more mature osteoblast-like phenotype that expressed characteristics of cellular differentiation and bone development. It was determined the two OS aggregoid models shared similarities of metabolic behaviour with different regions of OS human tissues, specifically of the higher metastatic grade.
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spelling pubmed-84015352021-08-29 Comparison of Osteosarcoma Aggregated Tumour Models with Human Tissue by Multimodal Mass Spectrometry Imaging Flint, Lucy E. Hamm, Gregory Ready, Joseph D. Ling, Stephanie Duckett, Catherine J. Cross, Neil A. Cole, Laura M. Smith, David P. Goodwin, Richard J. A. Clench, Malcolm R. Metabolites Article Osteosarcoma (OS) is the most common primary bone malignancy and largely effects adolescents and young adults, with 60% of patients under the age of 25. There are multiple cell models of OS described in vitro that express the specific genetic alterations of the sarcoma. In the work reported here, multiple mass spectrometry imaging (MSI) modalities were employed to characterise two aggregated cellular models of OS models formed using the MG63 and SAOS-2 cell lines. Phenotyping of the metabolite activity within the two OS aggregoid models was achieved and a comparison of the metabolite data with OS human tissue samples revealed relevant fatty acid and phospholipid markers. Although, annotations of these species require MS/MS analysis for confident identification of the metabolites. From the putative assignments however, it was suggested that the MG63 aggregoids are an aggressive tumour model that exhibited metastatic-like potential. Alternatively, the SAOS-2 aggregoids are more mature osteoblast-like phenotype that expressed characteristics of cellular differentiation and bone development. It was determined the two OS aggregoid models shared similarities of metabolic behaviour with different regions of OS human tissues, specifically of the higher metastatic grade. MDPI 2021-07-31 /pmc/articles/PMC8401535/ /pubmed/34436447 http://dx.doi.org/10.3390/metabo11080506 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Flint, Lucy E.
Hamm, Gregory
Ready, Joseph D.
Ling, Stephanie
Duckett, Catherine J.
Cross, Neil A.
Cole, Laura M.
Smith, David P.
Goodwin, Richard J. A.
Clench, Malcolm R.
Comparison of Osteosarcoma Aggregated Tumour Models with Human Tissue by Multimodal Mass Spectrometry Imaging
title Comparison of Osteosarcoma Aggregated Tumour Models with Human Tissue by Multimodal Mass Spectrometry Imaging
title_full Comparison of Osteosarcoma Aggregated Tumour Models with Human Tissue by Multimodal Mass Spectrometry Imaging
title_fullStr Comparison of Osteosarcoma Aggregated Tumour Models with Human Tissue by Multimodal Mass Spectrometry Imaging
title_full_unstemmed Comparison of Osteosarcoma Aggregated Tumour Models with Human Tissue by Multimodal Mass Spectrometry Imaging
title_short Comparison of Osteosarcoma Aggregated Tumour Models with Human Tissue by Multimodal Mass Spectrometry Imaging
title_sort comparison of osteosarcoma aggregated tumour models with human tissue by multimodal mass spectrometry imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8401535/
https://www.ncbi.nlm.nih.gov/pubmed/34436447
http://dx.doi.org/10.3390/metabo11080506
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