Cargando…
Fluid shear stress impacts ovarian cancer cell viability, subcellular organization, and promotes genomic instability
Ovarian cancer cells are exposed to physical stress in the peritoneal cavity during both tumor growth and dissemination. Ascites build-up in metastatic ovarian cancer further increases the exposure to fluid shear stress. Here, we used a murine, in vitro ovarian cancer progression model in parallel w...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864000/ https://www.ncbi.nlm.nih.gov/pubmed/29566010 http://dx.doi.org/10.1371/journal.pone.0194170 |
_version_ | 1783308470228877312 |
---|---|
author | Hyler, Alexandra R. Baudoin, Nicolaas C. Brown, Megan S. Stremler, Mark A. Cimini, Daniela Davalos, Rafael V. Schmelz, Eva M. |
author_facet | Hyler, Alexandra R. Baudoin, Nicolaas C. Brown, Megan S. Stremler, Mark A. Cimini, Daniela Davalos, Rafael V. Schmelz, Eva M. |
author_sort | Hyler, Alexandra R. |
collection | PubMed |
description | Ovarian cancer cells are exposed to physical stress in the peritoneal cavity during both tumor growth and dissemination. Ascites build-up in metastatic ovarian cancer further increases the exposure to fluid shear stress. Here, we used a murine, in vitro ovarian cancer progression model in parallel with immortalized human cells to investigate how ovarian cancer cells of increasing aggressiveness respond to [Image: see text] of fluid-induced shear stress. This biophysical stimulus significantly reduced cell viability in all cells exposed, independent of disease stage. Fluid shear stress induced spheroid formation and altered cytoskeleton organization in more tumorigenic cell lines. While benign ovarian cells appeared to survive in higher numbers under the influence of fluid shear stress, they exhibited severe morphological changes and chromosomal instability. These results suggest that exposure of benign cells to low magnitude fluid shear stress can induce phenotypic changes that are associated with transformation and ovarian cancer progression. Moreover, exposure of tumorigenic cells to fluid shear stress enhanced anchorage-independent survival, suggesting a role in promoting invasion and metastasis. |
format | Online Article Text |
id | pubmed-5864000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58640002018-03-28 Fluid shear stress impacts ovarian cancer cell viability, subcellular organization, and promotes genomic instability Hyler, Alexandra R. Baudoin, Nicolaas C. Brown, Megan S. Stremler, Mark A. Cimini, Daniela Davalos, Rafael V. Schmelz, Eva M. PLoS One Research Article Ovarian cancer cells are exposed to physical stress in the peritoneal cavity during both tumor growth and dissemination. Ascites build-up in metastatic ovarian cancer further increases the exposure to fluid shear stress. Here, we used a murine, in vitro ovarian cancer progression model in parallel with immortalized human cells to investigate how ovarian cancer cells of increasing aggressiveness respond to [Image: see text] of fluid-induced shear stress. This biophysical stimulus significantly reduced cell viability in all cells exposed, independent of disease stage. Fluid shear stress induced spheroid formation and altered cytoskeleton organization in more tumorigenic cell lines. While benign ovarian cells appeared to survive in higher numbers under the influence of fluid shear stress, they exhibited severe morphological changes and chromosomal instability. These results suggest that exposure of benign cells to low magnitude fluid shear stress can induce phenotypic changes that are associated with transformation and ovarian cancer progression. Moreover, exposure of tumorigenic cells to fluid shear stress enhanced anchorage-independent survival, suggesting a role in promoting invasion and metastasis. Public Library of Science 2018-03-22 /pmc/articles/PMC5864000/ /pubmed/29566010 http://dx.doi.org/10.1371/journal.pone.0194170 Text en © 2018 Hyler et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Hyler, Alexandra R. Baudoin, Nicolaas C. Brown, Megan S. Stremler, Mark A. Cimini, Daniela Davalos, Rafael V. Schmelz, Eva M. Fluid shear stress impacts ovarian cancer cell viability, subcellular organization, and promotes genomic instability |
title | Fluid shear stress impacts ovarian cancer cell viability, subcellular organization, and promotes genomic instability |
title_full | Fluid shear stress impacts ovarian cancer cell viability, subcellular organization, and promotes genomic instability |
title_fullStr | Fluid shear stress impacts ovarian cancer cell viability, subcellular organization, and promotes genomic instability |
title_full_unstemmed | Fluid shear stress impacts ovarian cancer cell viability, subcellular organization, and promotes genomic instability |
title_short | Fluid shear stress impacts ovarian cancer cell viability, subcellular organization, and promotes genomic instability |
title_sort | fluid shear stress impacts ovarian cancer cell viability, subcellular organization, and promotes genomic instability |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864000/ https://www.ncbi.nlm.nih.gov/pubmed/29566010 http://dx.doi.org/10.1371/journal.pone.0194170 |
work_keys_str_mv | AT hyleralexandrar fluidshearstressimpactsovariancancercellviabilitysubcellularorganizationandpromotesgenomicinstability AT baudoinnicolaasc fluidshearstressimpactsovariancancercellviabilitysubcellularorganizationandpromotesgenomicinstability AT brownmegans fluidshearstressimpactsovariancancercellviabilitysubcellularorganizationandpromotesgenomicinstability AT stremlermarka fluidshearstressimpactsovariancancercellviabilitysubcellularorganizationandpromotesgenomicinstability AT ciminidaniela fluidshearstressimpactsovariancancercellviabilitysubcellularorganizationandpromotesgenomicinstability AT davalosrafaelv fluidshearstressimpactsovariancancercellviabilitysubcellularorganizationandpromotesgenomicinstability AT schmelzevam fluidshearstressimpactsovariancancercellviabilitysubcellularorganizationandpromotesgenomicinstability |