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Electric Fields at Breast Cancer and Cancer Cell Collective Galvanotaxis

Cancer growth interferes with local ionic environments, membrane potentials, and transepithelial potentials, resulting in small electrical changes in the tumor microenvironment. Electrical fields (EFs) have significant effects on cancer cell migration (galvanotaxis/electrotaxis), however, their role...

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Autores principales: Zhu, Kan, Hum, Nicholas R., Reid, Brian, Sun, Qin, Loots, Gabriela G., Zhao, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250931/
https://www.ncbi.nlm.nih.gov/pubmed/32457381
http://dx.doi.org/10.1038/s41598-020-65566-0
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author Zhu, Kan
Hum, Nicholas R.
Reid, Brian
Sun, Qin
Loots, Gabriela G.
Zhao, Min
author_facet Zhu, Kan
Hum, Nicholas R.
Reid, Brian
Sun, Qin
Loots, Gabriela G.
Zhao, Min
author_sort Zhu, Kan
collection PubMed
description Cancer growth interferes with local ionic environments, membrane potentials, and transepithelial potentials, resulting in small electrical changes in the tumor microenvironment. Electrical fields (EFs) have significant effects on cancer cell migration (galvanotaxis/electrotaxis), however, their role as a regulator of cancer progression and metastasis is poorly understood. Here, we employed unique probe systems to characterize the electrical properties of cancer cells and their migratory ability under an EF. Subcutaneous tumors were established from a triple-negative murine breast cancer cell line (4T1), electric currents and potentials of tumors were measured using vibrating probe and glass microelectrodes, respectively. Steady outward and inward currents could be detected at different positions on the tumor surface and magnitudes of the electric currents on the tumor surface strongly correlated with tumor weights. Potential measurements also showed the non-homogeneous intratumor electric potentials. Cancer cell migration was then surveyed in the presence of EFs in vitro. Parental 4T1 cells and metastatic sublines in isolation showed random migration in EFs of physiological strength, whereas cells in monolayer migrated collectively to the anode. Our data contribute to an improved understanding of breast cancer metastasis, providing new evidence in support of an electrical mechanism that promotes this phenomenon.
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spelling pubmed-72509312020-06-04 Electric Fields at Breast Cancer and Cancer Cell Collective Galvanotaxis Zhu, Kan Hum, Nicholas R. Reid, Brian Sun, Qin Loots, Gabriela G. Zhao, Min Sci Rep Article Cancer growth interferes with local ionic environments, membrane potentials, and transepithelial potentials, resulting in small electrical changes in the tumor microenvironment. Electrical fields (EFs) have significant effects on cancer cell migration (galvanotaxis/electrotaxis), however, their role as a regulator of cancer progression and metastasis is poorly understood. Here, we employed unique probe systems to characterize the electrical properties of cancer cells and their migratory ability under an EF. Subcutaneous tumors were established from a triple-negative murine breast cancer cell line (4T1), electric currents and potentials of tumors were measured using vibrating probe and glass microelectrodes, respectively. Steady outward and inward currents could be detected at different positions on the tumor surface and magnitudes of the electric currents on the tumor surface strongly correlated with tumor weights. Potential measurements also showed the non-homogeneous intratumor electric potentials. Cancer cell migration was then surveyed in the presence of EFs in vitro. Parental 4T1 cells and metastatic sublines in isolation showed random migration in EFs of physiological strength, whereas cells in monolayer migrated collectively to the anode. Our data contribute to an improved understanding of breast cancer metastasis, providing new evidence in support of an electrical mechanism that promotes this phenomenon. Nature Publishing Group UK 2020-05-26 /pmc/articles/PMC7250931/ /pubmed/32457381 http://dx.doi.org/10.1038/s41598-020-65566-0 Text en © The Author(s) 2020 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
Zhu, Kan
Hum, Nicholas R.
Reid, Brian
Sun, Qin
Loots, Gabriela G.
Zhao, Min
Electric Fields at Breast Cancer and Cancer Cell Collective Galvanotaxis
title Electric Fields at Breast Cancer and Cancer Cell Collective Galvanotaxis
title_full Electric Fields at Breast Cancer and Cancer Cell Collective Galvanotaxis
title_fullStr Electric Fields at Breast Cancer and Cancer Cell Collective Galvanotaxis
title_full_unstemmed Electric Fields at Breast Cancer and Cancer Cell Collective Galvanotaxis
title_short Electric Fields at Breast Cancer and Cancer Cell Collective Galvanotaxis
title_sort electric fields at breast cancer and cancer cell collective galvanotaxis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250931/
https://www.ncbi.nlm.nih.gov/pubmed/32457381
http://dx.doi.org/10.1038/s41598-020-65566-0
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