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Influence of Silver Nanoparticles on the Growth of Ascitic and Solid Ehrlich Adenocarcinoma: Focus on Copper Metabolism

The link between copper metabolism and tumor progression motivated us to use copper chelators for suppression of tumor growth. We assume that silver nanoparticles (AgNPs) can be used for lowering bioavailable copper. Our assumption is based on the ability of Ag(I) ions released by AgNPs in biologica...

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Autores principales: Magazenkova, Daria N., Skomorokhova, Ekaterina A., Farroukh, Mohammad Al, Zharkova, Maria S., Jassem, Zena M., Rekina, Valeria E., Shamova, Olga V., Puchkova, Ludmila V., Ilyechova, Ekaterina Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10145613/
https://www.ncbi.nlm.nih.gov/pubmed/37111584
http://dx.doi.org/10.3390/pharmaceutics15041099
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author Magazenkova, Daria N.
Skomorokhova, Ekaterina A.
Farroukh, Mohammad Al
Zharkova, Maria S.
Jassem, Zena M.
Rekina, Valeria E.
Shamova, Olga V.
Puchkova, Ludmila V.
Ilyechova, Ekaterina Y.
author_facet Magazenkova, Daria N.
Skomorokhova, Ekaterina A.
Farroukh, Mohammad Al
Zharkova, Maria S.
Jassem, Zena M.
Rekina, Valeria E.
Shamova, Olga V.
Puchkova, Ludmila V.
Ilyechova, Ekaterina Y.
author_sort Magazenkova, Daria N.
collection PubMed
description The link between copper metabolism and tumor progression motivated us to use copper chelators for suppression of tumor growth. We assume that silver nanoparticles (AgNPs) can be used for lowering bioavailable copper. Our assumption is based on the ability of Ag(I) ions released by AgNPs in biological media and interfere with Cu(I) transport. Intervention of Ag(I) into copper metabolism leads to the replacement of copper by silver in ceruloplasmin and the decrease in bioavailable copper in the bloodstream. To check this assumption, mice with ascitic or solid Ehrlich adenocarcinoma (EAC) were treated with AgNPs using different protocols. Copper status indexes (copper concentration, ceruloplasmin protein level, and oxidase activity) were monitored to assess copper metabolism. The expression of copper-related genes was determined by real-time PCR in the liver and tumors, and copper and silver levels were measured by FAAS. Intraperitoneal AgNPs treatment beginning on the day of tumor inoculation enhanced mice survival, reduced the proliferation of ascitic EAC cells, and suppressed the activity of HIF1α, TNF-α and VEGFa genes. Topical treatment by the AgNPs, which was started together with the implantation of EAC cells in the thigh, also enhanced mice survival, decreased tumor growth, and repressed genes responsible for neovascularization. The advantages of silver-induced copper deficiency over copper chelators are discussed.
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spelling pubmed-101456132023-04-29 Influence of Silver Nanoparticles on the Growth of Ascitic and Solid Ehrlich Adenocarcinoma: Focus on Copper Metabolism Magazenkova, Daria N. Skomorokhova, Ekaterina A. Farroukh, Mohammad Al Zharkova, Maria S. Jassem, Zena M. Rekina, Valeria E. Shamova, Olga V. Puchkova, Ludmila V. Ilyechova, Ekaterina Y. Pharmaceutics Article The link between copper metabolism and tumor progression motivated us to use copper chelators for suppression of tumor growth. We assume that silver nanoparticles (AgNPs) can be used for lowering bioavailable copper. Our assumption is based on the ability of Ag(I) ions released by AgNPs in biological media and interfere with Cu(I) transport. Intervention of Ag(I) into copper metabolism leads to the replacement of copper by silver in ceruloplasmin and the decrease in bioavailable copper in the bloodstream. To check this assumption, mice with ascitic or solid Ehrlich adenocarcinoma (EAC) were treated with AgNPs using different protocols. Copper status indexes (copper concentration, ceruloplasmin protein level, and oxidase activity) were monitored to assess copper metabolism. The expression of copper-related genes was determined by real-time PCR in the liver and tumors, and copper and silver levels were measured by FAAS. Intraperitoneal AgNPs treatment beginning on the day of tumor inoculation enhanced mice survival, reduced the proliferation of ascitic EAC cells, and suppressed the activity of HIF1α, TNF-α and VEGFa genes. Topical treatment by the AgNPs, which was started together with the implantation of EAC cells in the thigh, also enhanced mice survival, decreased tumor growth, and repressed genes responsible for neovascularization. The advantages of silver-induced copper deficiency over copper chelators are discussed. MDPI 2023-03-29 /pmc/articles/PMC10145613/ /pubmed/37111584 http://dx.doi.org/10.3390/pharmaceutics15041099 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Magazenkova, Daria N.
Skomorokhova, Ekaterina A.
Farroukh, Mohammad Al
Zharkova, Maria S.
Jassem, Zena M.
Rekina, Valeria E.
Shamova, Olga V.
Puchkova, Ludmila V.
Ilyechova, Ekaterina Y.
Influence of Silver Nanoparticles on the Growth of Ascitic and Solid Ehrlich Adenocarcinoma: Focus on Copper Metabolism
title Influence of Silver Nanoparticles on the Growth of Ascitic and Solid Ehrlich Adenocarcinoma: Focus on Copper Metabolism
title_full Influence of Silver Nanoparticles on the Growth of Ascitic and Solid Ehrlich Adenocarcinoma: Focus on Copper Metabolism
title_fullStr Influence of Silver Nanoparticles on the Growth of Ascitic and Solid Ehrlich Adenocarcinoma: Focus on Copper Metabolism
title_full_unstemmed Influence of Silver Nanoparticles on the Growth of Ascitic and Solid Ehrlich Adenocarcinoma: Focus on Copper Metabolism
title_short Influence of Silver Nanoparticles on the Growth of Ascitic and Solid Ehrlich Adenocarcinoma: Focus on Copper Metabolism
title_sort influence of silver nanoparticles on the growth of ascitic and solid ehrlich adenocarcinoma: focus on copper metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10145613/
https://www.ncbi.nlm.nih.gov/pubmed/37111584
http://dx.doi.org/10.3390/pharmaceutics15041099
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