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A physical sciences network characterization of non-tumorigenic and metastatic cells

To investigate the transition from non-cancerous to metastatic from a physical sciences perspective, the Physical Sciences–Oncology Centers (PS-OC) Network performed molecular and biophysical comparative studies of the non-tumorigenic MCF-10A and metastatic MDA-MB-231 breast epithelial cell lines, c...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3636513/
https://www.ncbi.nlm.nih.gov/pubmed/23618955
http://dx.doi.org/10.1038/srep01449
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description To investigate the transition from non-cancerous to metastatic from a physical sciences perspective, the Physical Sciences–Oncology Centers (PS-OC) Network performed molecular and biophysical comparative studies of the non-tumorigenic MCF-10A and metastatic MDA-MB-231 breast epithelial cell lines, commonly used as models of cancer metastasis. Experiments were performed in 20 laboratories from 12 PS-OCs. Each laboratory was supplied with identical aliquots and common reagents and culture protocols. Analyses of these measurements revealed dramatic differences in their mechanics, migration, adhesion, oxygen response, and proteomic profiles. Model-based multi-omics approaches identified key differences between these cells' regulatory networks involved in morphology and survival. These results provide a multifaceted description of cellular parameters of two widely used cell lines and demonstrate the value of the PS-OC Network approach for integration of diverse experimental observations to elucidate the phenotypes associated with cancer metastasis.
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spelling pubmed-36365132013-04-29 A physical sciences network characterization of non-tumorigenic and metastatic cells Sci Rep Article To investigate the transition from non-cancerous to metastatic from a physical sciences perspective, the Physical Sciences–Oncology Centers (PS-OC) Network performed molecular and biophysical comparative studies of the non-tumorigenic MCF-10A and metastatic MDA-MB-231 breast epithelial cell lines, commonly used as models of cancer metastasis. Experiments were performed in 20 laboratories from 12 PS-OCs. Each laboratory was supplied with identical aliquots and common reagents and culture protocols. Analyses of these measurements revealed dramatic differences in their mechanics, migration, adhesion, oxygen response, and proteomic profiles. Model-based multi-omics approaches identified key differences between these cells' regulatory networks involved in morphology and survival. These results provide a multifaceted description of cellular parameters of two widely used cell lines and demonstrate the value of the PS-OC Network approach for integration of diverse experimental observations to elucidate the phenotypes associated with cancer metastasis. Nature Publishing Group 2013-04-26 /pmc/articles/PMC3636513/ /pubmed/23618955 http://dx.doi.org/10.1038/srep01449 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Article
A physical sciences network characterization of non-tumorigenic and metastatic cells
title A physical sciences network characterization of non-tumorigenic and metastatic cells
title_full A physical sciences network characterization of non-tumorigenic and metastatic cells
title_fullStr A physical sciences network characterization of non-tumorigenic and metastatic cells
title_full_unstemmed A physical sciences network characterization of non-tumorigenic and metastatic cells
title_short A physical sciences network characterization of non-tumorigenic and metastatic cells
title_sort physical sciences network characterization of non-tumorigenic and metastatic cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3636513/
https://www.ncbi.nlm.nih.gov/pubmed/23618955
http://dx.doi.org/10.1038/srep01449
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