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Low dose amiodarone reduces tumor growth and angiogenesis
Amiodarone is an anti-arrhythmic drug that was approved by the US Food and Drug Administration (FDA) in 1985. Pre-clinical studies suggest that Amiodarone induces cytotoxicity in several types of cancer cells, thus making it a potential candidate for use as an anti-cancer treatment. However, it is a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582908/ https://www.ncbi.nlm.nih.gov/pubmed/33093573 http://dx.doi.org/10.1038/s41598-020-75142-1 |
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author | Steinberg, Eliana Fluksman, Arnon Zemmour, Chalom Tischenko, Katerina Karsch-Bluman, Adi Brill-Karniely, Yifat Birsner, Amy E. D’Amato, Robert J. Benny, Ofra |
author_facet | Steinberg, Eliana Fluksman, Arnon Zemmour, Chalom Tischenko, Katerina Karsch-Bluman, Adi Brill-Karniely, Yifat Birsner, Amy E. D’Amato, Robert J. Benny, Ofra |
author_sort | Steinberg, Eliana |
collection | PubMed |
description | Amiodarone is an anti-arrhythmic drug that was approved by the US Food and Drug Administration (FDA) in 1985. Pre-clinical studies suggest that Amiodarone induces cytotoxicity in several types of cancer cells, thus making it a potential candidate for use as an anti-cancer treatment. However, it is also known to cause a variety of severe side effects. We hypothesized that in addition to the cytotoxic effects observed in cancer cells Amiodarone also has an indirect effect on angiogensis, a key factor in the tumor microenvironment. In this study, we examined Amiodarone's effects on a murine tumor model comprised of U-87 MG glioblastoma multiforme (GBM) cells, known to form highly vascularized tumors. We performed several in vitro assays using tumor and endothelial cells, along with in vivo assays utilizing three murine models. Low dose Amiodarone markedly reduced the size of GBM xenograft tumors and displayed a strong anti-angiogenic effect, suggesting dual cancer fighting properties. Our findings lay the ground for further research of Amiodarone as a possible clinical agent that, used in safe doses, maintains its dual properties while averting the drug’s harmful side effects. |
format | Online Article Text |
id | pubmed-7582908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75829082020-10-23 Low dose amiodarone reduces tumor growth and angiogenesis Steinberg, Eliana Fluksman, Arnon Zemmour, Chalom Tischenko, Katerina Karsch-Bluman, Adi Brill-Karniely, Yifat Birsner, Amy E. D’Amato, Robert J. Benny, Ofra Sci Rep Article Amiodarone is an anti-arrhythmic drug that was approved by the US Food and Drug Administration (FDA) in 1985. Pre-clinical studies suggest that Amiodarone induces cytotoxicity in several types of cancer cells, thus making it a potential candidate for use as an anti-cancer treatment. However, it is also known to cause a variety of severe side effects. We hypothesized that in addition to the cytotoxic effects observed in cancer cells Amiodarone also has an indirect effect on angiogensis, a key factor in the tumor microenvironment. In this study, we examined Amiodarone's effects on a murine tumor model comprised of U-87 MG glioblastoma multiforme (GBM) cells, known to form highly vascularized tumors. We performed several in vitro assays using tumor and endothelial cells, along with in vivo assays utilizing three murine models. Low dose Amiodarone markedly reduced the size of GBM xenograft tumors and displayed a strong anti-angiogenic effect, suggesting dual cancer fighting properties. Our findings lay the ground for further research of Amiodarone as a possible clinical agent that, used in safe doses, maintains its dual properties while averting the drug’s harmful side effects. Nature Publishing Group UK 2020-10-22 /pmc/articles/PMC7582908/ /pubmed/33093573 http://dx.doi.org/10.1038/s41598-020-75142-1 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 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/. |
spellingShingle | Article Steinberg, Eliana Fluksman, Arnon Zemmour, Chalom Tischenko, Katerina Karsch-Bluman, Adi Brill-Karniely, Yifat Birsner, Amy E. D’Amato, Robert J. Benny, Ofra Low dose amiodarone reduces tumor growth and angiogenesis |
title | Low dose amiodarone reduces tumor growth and angiogenesis |
title_full | Low dose amiodarone reduces tumor growth and angiogenesis |
title_fullStr | Low dose amiodarone reduces tumor growth and angiogenesis |
title_full_unstemmed | Low dose amiodarone reduces tumor growth and angiogenesis |
title_short | Low dose amiodarone reduces tumor growth and angiogenesis |
title_sort | low dose amiodarone reduces tumor growth and angiogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582908/ https://www.ncbi.nlm.nih.gov/pubmed/33093573 http://dx.doi.org/10.1038/s41598-020-75142-1 |
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