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Differential response of patient-derived primary glioblastoma cells to environmental stiffness
The ability of cancer cells to sense external mechanical forces has emerged as a significant factor in the promotion of cancer invasion. Currently there are conflicting reports in the literature with regard to whether glioblastoma (GBM) brain cancer cell migration and invasion is rigidity-sensitive....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800394/ https://www.ncbi.nlm.nih.gov/pubmed/26996336 http://dx.doi.org/10.1038/srep23353 |
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author | Grundy, Thomas James De Leon, Ellen Griffin, Kaitlyn Rose Stringer, Brett William Day, Bryan William Fabry, Ben Cooper-White, Justin O’Neill, Geraldine Margaret |
author_facet | Grundy, Thomas James De Leon, Ellen Griffin, Kaitlyn Rose Stringer, Brett William Day, Bryan William Fabry, Ben Cooper-White, Justin O’Neill, Geraldine Margaret |
author_sort | Grundy, Thomas James |
collection | PubMed |
description | The ability of cancer cells to sense external mechanical forces has emerged as a significant factor in the promotion of cancer invasion. Currently there are conflicting reports in the literature with regard to whether glioblastoma (GBM) brain cancer cell migration and invasion is rigidity-sensitive. In order to address this question we have compared the rigidity-response of primary patient-derived GBM lines. Cells were plated on polyacrylamide gels of defined rigidity that reflect the diversity of the brain tissue mechanical environment, and cell morphology and migration were analysed by time-lapse microscopy. Invasiveness was assessed in multicellular spheroids embedded in 3D matrigel cultures. Our data reveal a range of rigidity-dependent responses between the patient-derived cell lines, from reduced migration on the most compliant tissue stiffness to those that are insensitive to substrate rigidity and are equally migratory irrespective of the underlying substrate stiffness. Notably, the rigidity-insensitive GBM cells show the greatest invasive capacity in soft 3D matrigel cultures. Collectively our data confirm both rigidity-dependent and independent behaviour in primary GBM patient-derived cells. |
format | Online Article Text |
id | pubmed-4800394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48003942016-03-22 Differential response of patient-derived primary glioblastoma cells to environmental stiffness Grundy, Thomas James De Leon, Ellen Griffin, Kaitlyn Rose Stringer, Brett William Day, Bryan William Fabry, Ben Cooper-White, Justin O’Neill, Geraldine Margaret Sci Rep Article The ability of cancer cells to sense external mechanical forces has emerged as a significant factor in the promotion of cancer invasion. Currently there are conflicting reports in the literature with regard to whether glioblastoma (GBM) brain cancer cell migration and invasion is rigidity-sensitive. In order to address this question we have compared the rigidity-response of primary patient-derived GBM lines. Cells were plated on polyacrylamide gels of defined rigidity that reflect the diversity of the brain tissue mechanical environment, and cell morphology and migration were analysed by time-lapse microscopy. Invasiveness was assessed in multicellular spheroids embedded in 3D matrigel cultures. Our data reveal a range of rigidity-dependent responses between the patient-derived cell lines, from reduced migration on the most compliant tissue stiffness to those that are insensitive to substrate rigidity and are equally migratory irrespective of the underlying substrate stiffness. Notably, the rigidity-insensitive GBM cells show the greatest invasive capacity in soft 3D matrigel cultures. Collectively our data confirm both rigidity-dependent and independent behaviour in primary GBM patient-derived cells. Nature Publishing Group 2016-03-21 /pmc/articles/PMC4800394/ /pubmed/26996336 http://dx.doi.org/10.1038/srep23353 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Grundy, Thomas James De Leon, Ellen Griffin, Kaitlyn Rose Stringer, Brett William Day, Bryan William Fabry, Ben Cooper-White, Justin O’Neill, Geraldine Margaret Differential response of patient-derived primary glioblastoma cells to environmental stiffness |
title | Differential response of patient-derived primary glioblastoma cells to environmental stiffness |
title_full | Differential response of patient-derived primary glioblastoma cells to environmental stiffness |
title_fullStr | Differential response of patient-derived primary glioblastoma cells to environmental stiffness |
title_full_unstemmed | Differential response of patient-derived primary glioblastoma cells to environmental stiffness |
title_short | Differential response of patient-derived primary glioblastoma cells to environmental stiffness |
title_sort | differential response of patient-derived primary glioblastoma cells to environmental stiffness |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800394/ https://www.ncbi.nlm.nih.gov/pubmed/26996336 http://dx.doi.org/10.1038/srep23353 |
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