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Label-Free Recognition of Drug Resistance via Impedimetric Screening of Breast Cancer Cells

We present a novel study on label-free recognition and distinction of drug resistant breast cancer cells (MCF-7 DOX) from their parental cells (MCF-7 WT) via impedimetric measurements. Drug resistant cells exhibited significant differences in their dielectric properties compared to wild-type cells,...

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Autores principales: Eker, Bilge, Meissner, Robert, Bertsch, Arnaud, Mehta, Kapil, Renaud, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3587579/
https://www.ncbi.nlm.nih.gov/pubmed/23483910
http://dx.doi.org/10.1371/journal.pone.0057423
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author Eker, Bilge
Meissner, Robert
Bertsch, Arnaud
Mehta, Kapil
Renaud, Philippe
author_facet Eker, Bilge
Meissner, Robert
Bertsch, Arnaud
Mehta, Kapil
Renaud, Philippe
author_sort Eker, Bilge
collection PubMed
description We present a novel study on label-free recognition and distinction of drug resistant breast cancer cells (MCF-7 DOX) from their parental cells (MCF-7 WT) via impedimetric measurements. Drug resistant cells exhibited significant differences in their dielectric properties compared to wild-type cells, exerting much higher extracellular resistance (R(extra)). Immunostaining revealed that MCF-7 DOX cells gained a much denser F-actin network upon acquiring drug resistance indicating that remodeling of actin cytoskeleton is probably the reason behind higher R(extra), providing stronger cell architecture. Moreover, having exposed both cell types to doxorubicin, we were able to distinguish these two phenotypes based on their substantially different drug response. Interestingly, impedimetric measurements identified a concentration-dependent and reversible increase in cell stiffness in the presence of low non-lethal drug doses. Combined with a profound frequency analysis, these findings enabled distinguishing distinct cellular responses during drug exposure within four concentration ranges without using any labeling. Overall, this study highlights the possibility to differentiate drug resistant phenotypes from their parental cells and to assess their drug response by using microelectrodes, offering direct, real-time and noninvasive measurements of cell dependent parameters under drug exposure, hence providing a promising step for personalized medicine applications such as evaluation of the disease progress and optimization of the drug treatment of a patient during chemotherapy.
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spelling pubmed-35875792013-03-12 Label-Free Recognition of Drug Resistance via Impedimetric Screening of Breast Cancer Cells Eker, Bilge Meissner, Robert Bertsch, Arnaud Mehta, Kapil Renaud, Philippe PLoS One Research Article We present a novel study on label-free recognition and distinction of drug resistant breast cancer cells (MCF-7 DOX) from their parental cells (MCF-7 WT) via impedimetric measurements. Drug resistant cells exhibited significant differences in their dielectric properties compared to wild-type cells, exerting much higher extracellular resistance (R(extra)). Immunostaining revealed that MCF-7 DOX cells gained a much denser F-actin network upon acquiring drug resistance indicating that remodeling of actin cytoskeleton is probably the reason behind higher R(extra), providing stronger cell architecture. Moreover, having exposed both cell types to doxorubicin, we were able to distinguish these two phenotypes based on their substantially different drug response. Interestingly, impedimetric measurements identified a concentration-dependent and reversible increase in cell stiffness in the presence of low non-lethal drug doses. Combined with a profound frequency analysis, these findings enabled distinguishing distinct cellular responses during drug exposure within four concentration ranges without using any labeling. Overall, this study highlights the possibility to differentiate drug resistant phenotypes from their parental cells and to assess their drug response by using microelectrodes, offering direct, real-time and noninvasive measurements of cell dependent parameters under drug exposure, hence providing a promising step for personalized medicine applications such as evaluation of the disease progress and optimization of the drug treatment of a patient during chemotherapy. Public Library of Science 2013-03-04 /pmc/articles/PMC3587579/ /pubmed/23483910 http://dx.doi.org/10.1371/journal.pone.0057423 Text en © 2013 Eker 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Eker, Bilge
Meissner, Robert
Bertsch, Arnaud
Mehta, Kapil
Renaud, Philippe
Label-Free Recognition of Drug Resistance via Impedimetric Screening of Breast Cancer Cells
title Label-Free Recognition of Drug Resistance via Impedimetric Screening of Breast Cancer Cells
title_full Label-Free Recognition of Drug Resistance via Impedimetric Screening of Breast Cancer Cells
title_fullStr Label-Free Recognition of Drug Resistance via Impedimetric Screening of Breast Cancer Cells
title_full_unstemmed Label-Free Recognition of Drug Resistance via Impedimetric Screening of Breast Cancer Cells
title_short Label-Free Recognition of Drug Resistance via Impedimetric Screening of Breast Cancer Cells
title_sort label-free recognition of drug resistance via impedimetric screening of breast cancer cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3587579/
https://www.ncbi.nlm.nih.gov/pubmed/23483910
http://dx.doi.org/10.1371/journal.pone.0057423
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