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Electromagnetic fields alter the motility of metastatic breast cancer cells
Interactions between cells and their environment influence key physiologic processes such as their propensity to migrate. However, directed migration controlled by extrinsically applied electrical signals is poorly understood. Using a novel microfluidic platform, we found that metastatic breast canc...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687738/ https://www.ncbi.nlm.nih.gov/pubmed/31428691 http://dx.doi.org/10.1038/s42003-019-0550-z |
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author | Garg, Ayush Arpit Jones, Travis H. Moss, Sarah M. Mishra, Sanjay Kaul, Kirti Ahirwar, Dinesh K. Ferree, Jessica Kumar, Prabhat Subramaniam, Deepa Ganju, Ramesh K. Subramaniam, Vish V. Song, Jonathan W. |
author_facet | Garg, Ayush Arpit Jones, Travis H. Moss, Sarah M. Mishra, Sanjay Kaul, Kirti Ahirwar, Dinesh K. Ferree, Jessica Kumar, Prabhat Subramaniam, Deepa Ganju, Ramesh K. Subramaniam, Vish V. Song, Jonathan W. |
author_sort | Garg, Ayush Arpit |
collection | PubMed |
description | Interactions between cells and their environment influence key physiologic processes such as their propensity to migrate. However, directed migration controlled by extrinsically applied electrical signals is poorly understood. Using a novel microfluidic platform, we found that metastatic breast cancer cells sense and respond to the net direction of weak (∼100 µV cm(−1)), asymmetric, non-contact induced Electric Fields (iEFs). iEFs inhibited EGFR (Epidermal Growth Factor Receptor) activation, prevented formation of actin-rich filopodia, and hindered the motility of EGF-treated breast cancer cells. The directional effects of iEFs were nullified by inhibition of Akt phosphorylation. Moreover, iEFs in combination with Akt inhibitor reduced EGF-promoted motility below the level of untreated controls. These results represent a step towards isolating the coupling mechanism between cell motility and iEFs, provide valuable insights into how iEFs target multiple diverging cancer cell signaling mechanisms, and demonstrate that electrical signals are a fundamental regulator of cancer cell migration. |
format | Online Article Text |
id | pubmed-6687738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66877382019-08-19 Electromagnetic fields alter the motility of metastatic breast cancer cells Garg, Ayush Arpit Jones, Travis H. Moss, Sarah M. Mishra, Sanjay Kaul, Kirti Ahirwar, Dinesh K. Ferree, Jessica Kumar, Prabhat Subramaniam, Deepa Ganju, Ramesh K. Subramaniam, Vish V. Song, Jonathan W. Commun Biol Article Interactions between cells and their environment influence key physiologic processes such as their propensity to migrate. However, directed migration controlled by extrinsically applied electrical signals is poorly understood. Using a novel microfluidic platform, we found that metastatic breast cancer cells sense and respond to the net direction of weak (∼100 µV cm(−1)), asymmetric, non-contact induced Electric Fields (iEFs). iEFs inhibited EGFR (Epidermal Growth Factor Receptor) activation, prevented formation of actin-rich filopodia, and hindered the motility of EGF-treated breast cancer cells. The directional effects of iEFs were nullified by inhibition of Akt phosphorylation. Moreover, iEFs in combination with Akt inhibitor reduced EGF-promoted motility below the level of untreated controls. These results represent a step towards isolating the coupling mechanism between cell motility and iEFs, provide valuable insights into how iEFs target multiple diverging cancer cell signaling mechanisms, and demonstrate that electrical signals are a fundamental regulator of cancer cell migration. Nature Publishing Group UK 2019-08-08 /pmc/articles/PMC6687738/ /pubmed/31428691 http://dx.doi.org/10.1038/s42003-019-0550-z Text en © The Author(s) 2019 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 Garg, Ayush Arpit Jones, Travis H. Moss, Sarah M. Mishra, Sanjay Kaul, Kirti Ahirwar, Dinesh K. Ferree, Jessica Kumar, Prabhat Subramaniam, Deepa Ganju, Ramesh K. Subramaniam, Vish V. Song, Jonathan W. Electromagnetic fields alter the motility of metastatic breast cancer cells |
title | Electromagnetic fields alter the motility of metastatic breast cancer cells |
title_full | Electromagnetic fields alter the motility of metastatic breast cancer cells |
title_fullStr | Electromagnetic fields alter the motility of metastatic breast cancer cells |
title_full_unstemmed | Electromagnetic fields alter the motility of metastatic breast cancer cells |
title_short | Electromagnetic fields alter the motility of metastatic breast cancer cells |
title_sort | electromagnetic fields alter the motility of metastatic breast cancer cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687738/ https://www.ncbi.nlm.nih.gov/pubmed/31428691 http://dx.doi.org/10.1038/s42003-019-0550-z |
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