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Bioimpedimetric analysis in conjunction with growth dynamics to differentiate aggressiveness of cancer cells

Determination of cancer aggressiveness is mainly assessed in tissues by looking at the grade of cancer. There is a lack of specific method to determine aggressiveness of cancer cells in vitro. In our present work, we have proposed a bio-impedance based non-invasive method to differentiate aggressive...

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Autores principales: Parekh, Aditya, Das, Debanjan, Das, Subhayan, Dhara, Santanu, Biswas, Karabi, Mandal, Mahitosh, Das, Soumen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768811/
https://www.ncbi.nlm.nih.gov/pubmed/29335481
http://dx.doi.org/10.1038/s41598-017-18965-9
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author Parekh, Aditya
Das, Debanjan
Das, Subhayan
Dhara, Santanu
Biswas, Karabi
Mandal, Mahitosh
Das, Soumen
author_facet Parekh, Aditya
Das, Debanjan
Das, Subhayan
Dhara, Santanu
Biswas, Karabi
Mandal, Mahitosh
Das, Soumen
author_sort Parekh, Aditya
collection PubMed
description Determination of cancer aggressiveness is mainly assessed in tissues by looking at the grade of cancer. There is a lack of specific method to determine aggressiveness of cancer cells in vitro. In our present work, we have proposed a bio-impedance based non-invasive method to differentiate aggressive property of two breast cancer cell lines. Real-time impedance analysis of MCF-7 (less aggressive) and MDA-MB-231 cells (more aggressive) demonstrated unique growth pattern. Detailed slope-analysis of impedance curves at different growth phases showed that MDA-MB-231 had higher proliferation rate and intrinsic resistance to cell death, when allowed to grow in nutrient and space limiting conditions. This intrinsic nature of death resistance of MDA-MB-231 was due to modulation and elongation of filopodia, which was also observed during scanning electron microscopy. Results were also similar when validated by cell cycle analysis. Additionally, wavelet based analysis was used to demonstrate that MCF-7 had lesser micromotion based cellular activity, when compared with MDA-MB-231. Combined together, we hypothesize that analysis of growth rate, death resistance and cellular energy, through bioimpedance based analysis can be used to determine and compare aggressiveness of multiple cancer cell lines. This further opens avenues for extrapolation of present work to human tumor tissue samples.
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spelling pubmed-57688112018-01-25 Bioimpedimetric analysis in conjunction with growth dynamics to differentiate aggressiveness of cancer cells Parekh, Aditya Das, Debanjan Das, Subhayan Dhara, Santanu Biswas, Karabi Mandal, Mahitosh Das, Soumen Sci Rep Article Determination of cancer aggressiveness is mainly assessed in tissues by looking at the grade of cancer. There is a lack of specific method to determine aggressiveness of cancer cells in vitro. In our present work, we have proposed a bio-impedance based non-invasive method to differentiate aggressive property of two breast cancer cell lines. Real-time impedance analysis of MCF-7 (less aggressive) and MDA-MB-231 cells (more aggressive) demonstrated unique growth pattern. Detailed slope-analysis of impedance curves at different growth phases showed that MDA-MB-231 had higher proliferation rate and intrinsic resistance to cell death, when allowed to grow in nutrient and space limiting conditions. This intrinsic nature of death resistance of MDA-MB-231 was due to modulation and elongation of filopodia, which was also observed during scanning electron microscopy. Results were also similar when validated by cell cycle analysis. Additionally, wavelet based analysis was used to demonstrate that MCF-7 had lesser micromotion based cellular activity, when compared with MDA-MB-231. Combined together, we hypothesize that analysis of growth rate, death resistance and cellular energy, through bioimpedance based analysis can be used to determine and compare aggressiveness of multiple cancer cell lines. This further opens avenues for extrapolation of present work to human tumor tissue samples. Nature Publishing Group UK 2018-01-15 /pmc/articles/PMC5768811/ /pubmed/29335481 http://dx.doi.org/10.1038/s41598-017-18965-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Parekh, Aditya
Das, Debanjan
Das, Subhayan
Dhara, Santanu
Biswas, Karabi
Mandal, Mahitosh
Das, Soumen
Bioimpedimetric analysis in conjunction with growth dynamics to differentiate aggressiveness of cancer cells
title Bioimpedimetric analysis in conjunction with growth dynamics to differentiate aggressiveness of cancer cells
title_full Bioimpedimetric analysis in conjunction with growth dynamics to differentiate aggressiveness of cancer cells
title_fullStr Bioimpedimetric analysis in conjunction with growth dynamics to differentiate aggressiveness of cancer cells
title_full_unstemmed Bioimpedimetric analysis in conjunction with growth dynamics to differentiate aggressiveness of cancer cells
title_short Bioimpedimetric analysis in conjunction with growth dynamics to differentiate aggressiveness of cancer cells
title_sort bioimpedimetric analysis in conjunction with growth dynamics to differentiate aggressiveness of cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768811/
https://www.ncbi.nlm.nih.gov/pubmed/29335481
http://dx.doi.org/10.1038/s41598-017-18965-9
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