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Cellular shear stiffness reflects progression of arsenic-induced transformation during G(1)
Cancer cells consistently exhibit decreased stiffness; however, the onset and progression of this change have not been characterized. To study the development of cell stiffness changes, we evaluated the shear stiffness of populations of cells during transformation to a carcinogenic state. Bronchial...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862275/ https://www.ncbi.nlm.nih.gov/pubmed/29069374 http://dx.doi.org/10.1093/carcin/bgx116 |
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author | Muñoz, Alexandra Eldridge, Will J Jakobsen, Nina Munkholt Sørensen, Helle Wax, Adam Costa, Max |
author_facet | Muñoz, Alexandra Eldridge, Will J Jakobsen, Nina Munkholt Sørensen, Helle Wax, Adam Costa, Max |
author_sort | Muñoz, Alexandra |
collection | PubMed |
description | Cancer cells consistently exhibit decreased stiffness; however, the onset and progression of this change have not been characterized. To study the development of cell stiffness changes, we evaluated the shear stiffness of populations of cells during transformation to a carcinogenic state. Bronchial epithelial cells were exposed to sodium arsenite to initiate early stages of transformation. Exposed cells were cultured in soft agar to further transformation and select for clonal populations exhibiting anchorage-independent growth. Shear stiffness of various cell populations in G1 was assessed using a novel non-invasive assay that applies shear stress with fluid flow and evaluates nanoscale deformation using quantitative phase imaging (QPI). Arsenic-treated cells exhibited reduced stiffness relative to control cells, while arsenic clonal lines, selected by growth in soft agar, were found to have reduced stiffness relative to control clonal lines, which were cultured in soft agar but did not receive arsenic treatment. The relative standard deviation (RSD) of the stiffness of Arsenic clones was reduced compared with control clones, as well as to the arsenic-exposed cell population. Cell stiffness at the population level exhibits potential to be a novel and sensitive framework for identifying the development of cancerous cells. |
format | Online Article Text |
id | pubmed-5862275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58622752019-01-30 Cellular shear stiffness reflects progression of arsenic-induced transformation during G(1) Muñoz, Alexandra Eldridge, Will J Jakobsen, Nina Munkholt Sørensen, Helle Wax, Adam Costa, Max Carcinogenesis Cancer Biomarkers and Molecular Epidemiology Cancer cells consistently exhibit decreased stiffness; however, the onset and progression of this change have not been characterized. To study the development of cell stiffness changes, we evaluated the shear stiffness of populations of cells during transformation to a carcinogenic state. Bronchial epithelial cells were exposed to sodium arsenite to initiate early stages of transformation. Exposed cells were cultured in soft agar to further transformation and select for clonal populations exhibiting anchorage-independent growth. Shear stiffness of various cell populations in G1 was assessed using a novel non-invasive assay that applies shear stress with fluid flow and evaluates nanoscale deformation using quantitative phase imaging (QPI). Arsenic-treated cells exhibited reduced stiffness relative to control cells, while arsenic clonal lines, selected by growth in soft agar, were found to have reduced stiffness relative to control clonal lines, which were cultured in soft agar but did not receive arsenic treatment. The relative standard deviation (RSD) of the stiffness of Arsenic clones was reduced compared with control clones, as well as to the arsenic-exposed cell population. Cell stiffness at the population level exhibits potential to be a novel and sensitive framework for identifying the development of cancerous cells. Oxford University Press 2018-02 2017-10-24 /pmc/articles/PMC5862275/ /pubmed/29069374 http://dx.doi.org/10.1093/carcin/bgx116 Text en © The Author(s) 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Cancer Biomarkers and Molecular Epidemiology Muñoz, Alexandra Eldridge, Will J Jakobsen, Nina Munkholt Sørensen, Helle Wax, Adam Costa, Max Cellular shear stiffness reflects progression of arsenic-induced transformation during G(1) |
title | Cellular shear stiffness reflects progression of arsenic-induced transformation during G(1) |
title_full | Cellular shear stiffness reflects progression of arsenic-induced transformation during G(1) |
title_fullStr | Cellular shear stiffness reflects progression of arsenic-induced transformation during G(1) |
title_full_unstemmed | Cellular shear stiffness reflects progression of arsenic-induced transformation during G(1) |
title_short | Cellular shear stiffness reflects progression of arsenic-induced transformation during G(1) |
title_sort | cellular shear stiffness reflects progression of arsenic-induced transformation during g(1) |
topic | Cancer Biomarkers and Molecular Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862275/ https://www.ncbi.nlm.nih.gov/pubmed/29069374 http://dx.doi.org/10.1093/carcin/bgx116 |
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