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Engineering a 3D microfluidic culture platform for tumor-treating field application
The limitations of current cancer therapies highlight the urgent need for a more effective therapeutic strategy. One promising approach uses an alternating electric field; however, the mechanisms involved in the disruption of the cancer cell cycle as well as the potential adverse effects on non-canc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877588/ https://www.ncbi.nlm.nih.gov/pubmed/27215466 http://dx.doi.org/10.1038/srep26584 |
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author | Pavesi, Andrea Adriani, Giulia Tay, Andy Warkiani, Majid Ebrahimi Yeap, Wei Hseun Wong, Siew Cheng Kamm, Roger D. |
author_facet | Pavesi, Andrea Adriani, Giulia Tay, Andy Warkiani, Majid Ebrahimi Yeap, Wei Hseun Wong, Siew Cheng Kamm, Roger D. |
author_sort | Pavesi, Andrea |
collection | PubMed |
description | The limitations of current cancer therapies highlight the urgent need for a more effective therapeutic strategy. One promising approach uses an alternating electric field; however, the mechanisms involved in the disruption of the cancer cell cycle as well as the potential adverse effects on non-cancerous cells must be clarified. In this study, we present a novel microfluidic device with embedded electrodes that enables the application of an alternating electric field therapy to cancer cells in a 3D extracellular matrix. To demonstrate the potential of our system to aid in designing and testing new therapeutic approaches, cancer cells and cancer cell aggregates were cultured individually or co-cultured with endothelial cells. The metastatic potential of the cancer cells was reduced after electric field treatment. Moreover, the proliferation rate of the treated cancer cells was lower compared with that of the untreated cells, whereas the morphologies and proliferative capacities of the endothelial cells were not significantly affected. These results demonstrate that our novel system can be used to rapidly screen the effect of an alternating electric field on cancer and normal cells within an in vivo-like microenvironment with the potential to optimize treatment protocols and evaluate synergies between tumor-treating field treatment and chemotherapy. |
format | Online Article Text |
id | pubmed-4877588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48775882016-06-08 Engineering a 3D microfluidic culture platform for tumor-treating field application Pavesi, Andrea Adriani, Giulia Tay, Andy Warkiani, Majid Ebrahimi Yeap, Wei Hseun Wong, Siew Cheng Kamm, Roger D. Sci Rep Article The limitations of current cancer therapies highlight the urgent need for a more effective therapeutic strategy. One promising approach uses an alternating electric field; however, the mechanisms involved in the disruption of the cancer cell cycle as well as the potential adverse effects on non-cancerous cells must be clarified. In this study, we present a novel microfluidic device with embedded electrodes that enables the application of an alternating electric field therapy to cancer cells in a 3D extracellular matrix. To demonstrate the potential of our system to aid in designing and testing new therapeutic approaches, cancer cells and cancer cell aggregates were cultured individually or co-cultured with endothelial cells. The metastatic potential of the cancer cells was reduced after electric field treatment. Moreover, the proliferation rate of the treated cancer cells was lower compared with that of the untreated cells, whereas the morphologies and proliferative capacities of the endothelial cells were not significantly affected. These results demonstrate that our novel system can be used to rapidly screen the effect of an alternating electric field on cancer and normal cells within an in vivo-like microenvironment with the potential to optimize treatment protocols and evaluate synergies between tumor-treating field treatment and chemotherapy. Nature Publishing Group 2016-05-24 /pmc/articles/PMC4877588/ /pubmed/27215466 http://dx.doi.org/10.1038/srep26584 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Pavesi, Andrea Adriani, Giulia Tay, Andy Warkiani, Majid Ebrahimi Yeap, Wei Hseun Wong, Siew Cheng Kamm, Roger D. Engineering a 3D microfluidic culture platform for tumor-treating field application |
title | Engineering a 3D microfluidic culture platform for tumor-treating field application |
title_full | Engineering a 3D microfluidic culture platform for tumor-treating field application |
title_fullStr | Engineering a 3D microfluidic culture platform for tumor-treating field application |
title_full_unstemmed | Engineering a 3D microfluidic culture platform for tumor-treating field application |
title_short | Engineering a 3D microfluidic culture platform for tumor-treating field application |
title_sort | engineering a 3d microfluidic culture platform for tumor-treating field application |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877588/ https://www.ncbi.nlm.nih.gov/pubmed/27215466 http://dx.doi.org/10.1038/srep26584 |
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