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In Vitro Study of the Multimodal Effect of Na(+)/K(+) ATPase Blocker Ouabain on the Tumor Microenvironment and Malignant Cells

Na(+)/K(+) ATPase is a protein involved in the active transport of ions across the cellular membrane. Ouabain is a cardiotonic glycoside that, by inhibiting the Na(+)/K(+) pump, interferes with cell processes mediated directly by the pump, but also indirectly influences other cellular processes such...

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Autores principales: Harich, Octavia-Oana, Gavriliuc, Oana-Isabella, Ordodi, Valentin-Laurentiu, Tirziu, Alexandru, Paunescu, Virgil, Panaitescu, Carmen, Bojin, Maria-Florina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452365/
https://www.ncbi.nlm.nih.gov/pubmed/37626702
http://dx.doi.org/10.3390/biomedicines11082205
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author Harich, Octavia-Oana
Gavriliuc, Oana-Isabella
Ordodi, Valentin-Laurentiu
Tirziu, Alexandru
Paunescu, Virgil
Panaitescu, Carmen
Bojin, Maria-Florina
author_facet Harich, Octavia-Oana
Gavriliuc, Oana-Isabella
Ordodi, Valentin-Laurentiu
Tirziu, Alexandru
Paunescu, Virgil
Panaitescu, Carmen
Bojin, Maria-Florina
author_sort Harich, Octavia-Oana
collection PubMed
description Na(+)/K(+) ATPase is a protein involved in the active transport of ions across the cellular membrane. Ouabain is a cardiotonic glycoside that, by inhibiting the Na(+)/K(+) pump, interferes with cell processes mediated directly by the pump, but also indirectly influences other cellular processes such as cell cycle and proliferation, growth, cell differentiation, angiogenesis, migration, adhesion, and invasion. We used the SK-BR-3 breast cancer cell line, mesenchymal stem cells (MSCs), and tumor-associated fibroblasts (TAFs) in vitro to determine the effects of ouabain exposure on these cellular types. The results showed a multi-level effect of ouabain mainly on tumor cells, in a dose-dependent manner, while the TAFs and their normal counterparts were not significantly influenced. Following exposure to ouabain, the SK-BR-3 cells changed their morphologic appearance, decreased the expression of immunophenotypic markers (CD29, Her2, VEGF), the proliferation rate was significantly decreased (Ki67 index), the cells were blocked in the G(0) phase of the cell cycle and suffered necrosis. These data were correlated with the variable expression of α and β Na(+)/K(+) pump subunits in tumor cells, resulting in decreased ability to adhere to the VCAM-1 substrate in functional flow chamber studies. Being indicative of the pro-apoptotic and inhibitory effect of ouabain on tumor invasion and metastasis, the results support the addition of ouabain to the oncological therapeutic arsenal, trailing the “repurposing drugs” approach.
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spelling pubmed-104523652023-08-26 In Vitro Study of the Multimodal Effect of Na(+)/K(+) ATPase Blocker Ouabain on the Tumor Microenvironment and Malignant Cells Harich, Octavia-Oana Gavriliuc, Oana-Isabella Ordodi, Valentin-Laurentiu Tirziu, Alexandru Paunescu, Virgil Panaitescu, Carmen Bojin, Maria-Florina Biomedicines Article Na(+)/K(+) ATPase is a protein involved in the active transport of ions across the cellular membrane. Ouabain is a cardiotonic glycoside that, by inhibiting the Na(+)/K(+) pump, interferes with cell processes mediated directly by the pump, but also indirectly influences other cellular processes such as cell cycle and proliferation, growth, cell differentiation, angiogenesis, migration, adhesion, and invasion. We used the SK-BR-3 breast cancer cell line, mesenchymal stem cells (MSCs), and tumor-associated fibroblasts (TAFs) in vitro to determine the effects of ouabain exposure on these cellular types. The results showed a multi-level effect of ouabain mainly on tumor cells, in a dose-dependent manner, while the TAFs and their normal counterparts were not significantly influenced. Following exposure to ouabain, the SK-BR-3 cells changed their morphologic appearance, decreased the expression of immunophenotypic markers (CD29, Her2, VEGF), the proliferation rate was significantly decreased (Ki67 index), the cells were blocked in the G(0) phase of the cell cycle and suffered necrosis. These data were correlated with the variable expression of α and β Na(+)/K(+) pump subunits in tumor cells, resulting in decreased ability to adhere to the VCAM-1 substrate in functional flow chamber studies. Being indicative of the pro-apoptotic and inhibitory effect of ouabain on tumor invasion and metastasis, the results support the addition of ouabain to the oncological therapeutic arsenal, trailing the “repurposing drugs” approach. MDPI 2023-08-05 /pmc/articles/PMC10452365/ /pubmed/37626702 http://dx.doi.org/10.3390/biomedicines11082205 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
Harich, Octavia-Oana
Gavriliuc, Oana-Isabella
Ordodi, Valentin-Laurentiu
Tirziu, Alexandru
Paunescu, Virgil
Panaitescu, Carmen
Bojin, Maria-Florina
In Vitro Study of the Multimodal Effect of Na(+)/K(+) ATPase Blocker Ouabain on the Tumor Microenvironment and Malignant Cells
title In Vitro Study of the Multimodal Effect of Na(+)/K(+) ATPase Blocker Ouabain on the Tumor Microenvironment and Malignant Cells
title_full In Vitro Study of the Multimodal Effect of Na(+)/K(+) ATPase Blocker Ouabain on the Tumor Microenvironment and Malignant Cells
title_fullStr In Vitro Study of the Multimodal Effect of Na(+)/K(+) ATPase Blocker Ouabain on the Tumor Microenvironment and Malignant Cells
title_full_unstemmed In Vitro Study of the Multimodal Effect of Na(+)/K(+) ATPase Blocker Ouabain on the Tumor Microenvironment and Malignant Cells
title_short In Vitro Study of the Multimodal Effect of Na(+)/K(+) ATPase Blocker Ouabain on the Tumor Microenvironment and Malignant Cells
title_sort in vitro study of the multimodal effect of na(+)/k(+) atpase blocker ouabain on the tumor microenvironment and malignant cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452365/
https://www.ncbi.nlm.nih.gov/pubmed/37626702
http://dx.doi.org/10.3390/biomedicines11082205
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