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Interactions of Cisplatin and Daunorubicin at the Chromatin Level
Unexpectedly, the widely used anticancer agents Cisplatin (Cis-Pt) and Daunorubicin (Dauno) exhibited cell type- and concentration-dependent synergy or antagonism in vitro. We attempted to interpret these effects in terms of the changes elicited by the drugs in the chromatin, the target held primari...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981277/ https://www.ncbi.nlm.nih.gov/pubmed/31980698 http://dx.doi.org/10.1038/s41598-020-57702-7 |
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author | Firouzi Niaki, Erfaneh Van Acker, Thibaut Imre, László Nánási, Péter Tarapcsák, Szabolcs Bacsó, Zsolt Vanhaecke, Frank Szabó, Gábor |
author_facet | Firouzi Niaki, Erfaneh Van Acker, Thibaut Imre, László Nánási, Péter Tarapcsák, Szabolcs Bacsó, Zsolt Vanhaecke, Frank Szabó, Gábor |
author_sort | Firouzi Niaki, Erfaneh |
collection | PubMed |
description | Unexpectedly, the widely used anticancer agents Cisplatin (Cis-Pt) and Daunorubicin (Dauno) exhibited cell type- and concentration-dependent synergy or antagonism in vitro. We attempted to interpret these effects in terms of the changes elicited by the drugs in the chromatin, the target held primarily responsible for the cytotoxicity of both agents. We measured the effect of Cis-Pt on the levels of Dauno in different cell compartments, the effect of Cis-Pt on Dauno-induced nucleosome eviction, and assessed the influence of Dauno on DNA platination in flow- and laser scanning cytometry as well as in laser ablation-inductively coupled plasma-mass spectrometry assays. We show that the two drugs antagonize each other through a decrease of interstrand crosslinks upon co-treatment with Dauno, and also via the diminished Dauno uptake in the presence of Cis-Pt, and both effects are observed already at low Dauno concentrations. At high Dauno concentrations synergy becomes dominant because histone eviction by Dauno intercalation into the DNA is enhanced in the presence of co-treatment with Cis-Pt. These interactions may have an impact on the efficacy of combination treatment protocols, considering the long retention time of DNA adducts formed by both agents. |
format | Online Article Text |
id | pubmed-6981277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69812772020-01-30 Interactions of Cisplatin and Daunorubicin at the Chromatin Level Firouzi Niaki, Erfaneh Van Acker, Thibaut Imre, László Nánási, Péter Tarapcsák, Szabolcs Bacsó, Zsolt Vanhaecke, Frank Szabó, Gábor Sci Rep Article Unexpectedly, the widely used anticancer agents Cisplatin (Cis-Pt) and Daunorubicin (Dauno) exhibited cell type- and concentration-dependent synergy or antagonism in vitro. We attempted to interpret these effects in terms of the changes elicited by the drugs in the chromatin, the target held primarily responsible for the cytotoxicity of both agents. We measured the effect of Cis-Pt on the levels of Dauno in different cell compartments, the effect of Cis-Pt on Dauno-induced nucleosome eviction, and assessed the influence of Dauno on DNA platination in flow- and laser scanning cytometry as well as in laser ablation-inductively coupled plasma-mass spectrometry assays. We show that the two drugs antagonize each other through a decrease of interstrand crosslinks upon co-treatment with Dauno, and also via the diminished Dauno uptake in the presence of Cis-Pt, and both effects are observed already at low Dauno concentrations. At high Dauno concentrations synergy becomes dominant because histone eviction by Dauno intercalation into the DNA is enhanced in the presence of co-treatment with Cis-Pt. These interactions may have an impact on the efficacy of combination treatment protocols, considering the long retention time of DNA adducts formed by both agents. Nature Publishing Group UK 2020-01-24 /pmc/articles/PMC6981277/ /pubmed/31980698 http://dx.doi.org/10.1038/s41598-020-57702-7 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 Firouzi Niaki, Erfaneh Van Acker, Thibaut Imre, László Nánási, Péter Tarapcsák, Szabolcs Bacsó, Zsolt Vanhaecke, Frank Szabó, Gábor Interactions of Cisplatin and Daunorubicin at the Chromatin Level |
title | Interactions of Cisplatin and Daunorubicin at the Chromatin Level |
title_full | Interactions of Cisplatin and Daunorubicin at the Chromatin Level |
title_fullStr | Interactions of Cisplatin and Daunorubicin at the Chromatin Level |
title_full_unstemmed | Interactions of Cisplatin and Daunorubicin at the Chromatin Level |
title_short | Interactions of Cisplatin and Daunorubicin at the Chromatin Level |
title_sort | interactions of cisplatin and daunorubicin at the chromatin level |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981277/ https://www.ncbi.nlm.nih.gov/pubmed/31980698 http://dx.doi.org/10.1038/s41598-020-57702-7 |
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