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Optimization of tumor-treating field therapy for triple-negative breast cancer cells in vitro via frequency modulation

PURPOSE: Currently, tumor-treating field (TTField) therapy utilizes a single “optimal” frequency of electric fields to achieve maximal cell death in a targeted population of cells. However, because of differences in cell size, shape, and ploidy during mitosis, optimal electric field characteristics...

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Autores principales: Smothers, Austin R., Henderson, Jason R., O’Connell, John J., Stenbeck, Jonathan M., Dean, Delphine, Booth, Brian W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245511/
https://www.ncbi.nlm.nih.gov/pubmed/37287008
http://dx.doi.org/10.1186/s12935-023-02959-x
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author Smothers, Austin R.
Henderson, Jason R.
O’Connell, John J.
Stenbeck, Jonathan M.
Dean, Delphine
Booth, Brian W.
author_facet Smothers, Austin R.
Henderson, Jason R.
O’Connell, John J.
Stenbeck, Jonathan M.
Dean, Delphine
Booth, Brian W.
author_sort Smothers, Austin R.
collection PubMed
description PURPOSE: Currently, tumor-treating field (TTField) therapy utilizes a single “optimal” frequency of electric fields to achieve maximal cell death in a targeted population of cells. However, because of differences in cell size, shape, and ploidy during mitosis, optimal electric field characteristics for universal maximal cell death may not exist. This study investigated the anti-mitotic effects of modulating electric field frequency as opposed to utilizing uniform electric fields. METHODS: We developed and validated a custom device that delivers a wide variety of electric field and treatment parameters including frequency modulation. We investigated the efficacy of frequency modulating tumor-treating fields on triple-negative breast cancer cells compared to human breast epithelial cells. RESULTS: We show that frequency-modulated (FM) TTFields are as selective at treating triple-negative breast cancer (TNBC) as uniform TTFields while having a greater efficacy for combating TNBC cell growth. TTField treatment at a mean frequency of 150 kHz with a frequency range of ± 10 kHz induced apoptosis in a greater number of TNBC cells after 24 h as compared to unmodulated treatment which led to further decreased cell viability after 48 h. Furthermore, all TNBC cells died after 72 h of FM treatment while cells that received unmodulated treatment were able to recover to cell number equivalent to the control. CONCLUSION: TTFields were highly efficacious against TNBC growth, FM TTFields showed minimal effects on epithelial cells similar to unmodulated treatment.
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spelling pubmed-102455112023-06-08 Optimization of tumor-treating field therapy for triple-negative breast cancer cells in vitro via frequency modulation Smothers, Austin R. Henderson, Jason R. O’Connell, John J. Stenbeck, Jonathan M. Dean, Delphine Booth, Brian W. Cancer Cell Int Research PURPOSE: Currently, tumor-treating field (TTField) therapy utilizes a single “optimal” frequency of electric fields to achieve maximal cell death in a targeted population of cells. However, because of differences in cell size, shape, and ploidy during mitosis, optimal electric field characteristics for universal maximal cell death may not exist. This study investigated the anti-mitotic effects of modulating electric field frequency as opposed to utilizing uniform electric fields. METHODS: We developed and validated a custom device that delivers a wide variety of electric field and treatment parameters including frequency modulation. We investigated the efficacy of frequency modulating tumor-treating fields on triple-negative breast cancer cells compared to human breast epithelial cells. RESULTS: We show that frequency-modulated (FM) TTFields are as selective at treating triple-negative breast cancer (TNBC) as uniform TTFields while having a greater efficacy for combating TNBC cell growth. TTField treatment at a mean frequency of 150 kHz with a frequency range of ± 10 kHz induced apoptosis in a greater number of TNBC cells after 24 h as compared to unmodulated treatment which led to further decreased cell viability after 48 h. Furthermore, all TNBC cells died after 72 h of FM treatment while cells that received unmodulated treatment were able to recover to cell number equivalent to the control. CONCLUSION: TTFields were highly efficacious against TNBC growth, FM TTFields showed minimal effects on epithelial cells similar to unmodulated treatment. BioMed Central 2023-06-07 /pmc/articles/PMC10245511/ /pubmed/37287008 http://dx.doi.org/10.1186/s12935-023-02959-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Smothers, Austin R.
Henderson, Jason R.
O’Connell, John J.
Stenbeck, Jonathan M.
Dean, Delphine
Booth, Brian W.
Optimization of tumor-treating field therapy for triple-negative breast cancer cells in vitro via frequency modulation
title Optimization of tumor-treating field therapy for triple-negative breast cancer cells in vitro via frequency modulation
title_full Optimization of tumor-treating field therapy for triple-negative breast cancer cells in vitro via frequency modulation
title_fullStr Optimization of tumor-treating field therapy for triple-negative breast cancer cells in vitro via frequency modulation
title_full_unstemmed Optimization of tumor-treating field therapy for triple-negative breast cancer cells in vitro via frequency modulation
title_short Optimization of tumor-treating field therapy for triple-negative breast cancer cells in vitro via frequency modulation
title_sort optimization of tumor-treating field therapy for triple-negative breast cancer cells in vitro via frequency modulation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245511/
https://www.ncbi.nlm.nih.gov/pubmed/37287008
http://dx.doi.org/10.1186/s12935-023-02959-x
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