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In Vitro and Computational Studies of Perezone and Perezone Angelate as Potential Anti-Glioblastoma Multiforme Agents

Glioblastoma multiforme (GBM) represents the most malignant type of astrocytoma, with a life expectancy of two years. It has been shown that Poly (ADP-ribose) polymerase 1 (PARP-1) protein is over-expressed in GBM cells, while its expression in healthy tissue is low. In addition, perezone, a phyto-c...

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Autores principales: Hernández-Rodríguez, Maricarmen, Mendoza Sánchez, Pablo I., Martínez, Joel, Macías Pérez, Martha E., Rosales Cruz, Erika, Żołek, Teresa, Maciejewska, Dorota, Miranda Ruvalcaba, René, Mera Jiménez, Elvia, Nicolás-Vázquez, María I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911992/
https://www.ncbi.nlm.nih.gov/pubmed/35268667
http://dx.doi.org/10.3390/molecules27051565
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author Hernández-Rodríguez, Maricarmen
Mendoza Sánchez, Pablo I.
Martínez, Joel
Macías Pérez, Martha E.
Rosales Cruz, Erika
Żołek, Teresa
Maciejewska, Dorota
Miranda Ruvalcaba, René
Mera Jiménez, Elvia
Nicolás-Vázquez, María I.
author_facet Hernández-Rodríguez, Maricarmen
Mendoza Sánchez, Pablo I.
Martínez, Joel
Macías Pérez, Martha E.
Rosales Cruz, Erika
Żołek, Teresa
Maciejewska, Dorota
Miranda Ruvalcaba, René
Mera Jiménez, Elvia
Nicolás-Vázquez, María I.
author_sort Hernández-Rodríguez, Maricarmen
collection PubMed
description Glioblastoma multiforme (GBM) represents the most malignant type of astrocytoma, with a life expectancy of two years. It has been shown that Poly (ADP-ribose) polymerase 1 (PARP-1) protein is over-expressed in GBM cells, while its expression in healthy tissue is low. In addition, perezone, a phyto-compound, is a PARP-1 inhibitor with anti-neoplastic activity. As a consequence, in the present study, both in vitro and computational evaluations of perezone and its chemically related compound, perezone angelate, as anti-GBM agents were performed. Hence, the anti-proliferative assay showed that perezone angelate induces higher cytotoxicity in the GBM cell line (U373 IC(50) = 6.44 μM) than perezone (U373 IC(50) = 51.20 μM) by induction of apoptosis. In addition, perezone angelate showed low cytotoxic activity in rat glial cells (IC(50) = 173.66 μM). PARP-1 inhibitory activity (IC(50) = 5.25 μM) and oxidative stress induction by perezone angelate were corroborated employing in vitro studies. In the other hand, the performed docking studies allowed explaining the PARP-1 inhibitory activity of perezone angelate, and ADMET studies showed its probability to permeate cell membranes and the blood–brain barrier, which is an essential characteristic of drugs to treat neurological diseases. Finally, it is essential to highlight that the results confirm perezone angelate as a potential anti-GBM agent.
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spelling pubmed-89119922022-03-11 In Vitro and Computational Studies of Perezone and Perezone Angelate as Potential Anti-Glioblastoma Multiforme Agents Hernández-Rodríguez, Maricarmen Mendoza Sánchez, Pablo I. Martínez, Joel Macías Pérez, Martha E. Rosales Cruz, Erika Żołek, Teresa Maciejewska, Dorota Miranda Ruvalcaba, René Mera Jiménez, Elvia Nicolás-Vázquez, María I. Molecules Article Glioblastoma multiforme (GBM) represents the most malignant type of astrocytoma, with a life expectancy of two years. It has been shown that Poly (ADP-ribose) polymerase 1 (PARP-1) protein is over-expressed in GBM cells, while its expression in healthy tissue is low. In addition, perezone, a phyto-compound, is a PARP-1 inhibitor with anti-neoplastic activity. As a consequence, in the present study, both in vitro and computational evaluations of perezone and its chemically related compound, perezone angelate, as anti-GBM agents were performed. Hence, the anti-proliferative assay showed that perezone angelate induces higher cytotoxicity in the GBM cell line (U373 IC(50) = 6.44 μM) than perezone (U373 IC(50) = 51.20 μM) by induction of apoptosis. In addition, perezone angelate showed low cytotoxic activity in rat glial cells (IC(50) = 173.66 μM). PARP-1 inhibitory activity (IC(50) = 5.25 μM) and oxidative stress induction by perezone angelate were corroborated employing in vitro studies. In the other hand, the performed docking studies allowed explaining the PARP-1 inhibitory activity of perezone angelate, and ADMET studies showed its probability to permeate cell membranes and the blood–brain barrier, which is an essential characteristic of drugs to treat neurological diseases. Finally, it is essential to highlight that the results confirm perezone angelate as a potential anti-GBM agent. MDPI 2022-02-26 /pmc/articles/PMC8911992/ /pubmed/35268667 http://dx.doi.org/10.3390/molecules27051565 Text en © 2022 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
Hernández-Rodríguez, Maricarmen
Mendoza Sánchez, Pablo I.
Martínez, Joel
Macías Pérez, Martha E.
Rosales Cruz, Erika
Żołek, Teresa
Maciejewska, Dorota
Miranda Ruvalcaba, René
Mera Jiménez, Elvia
Nicolás-Vázquez, María I.
In Vitro and Computational Studies of Perezone and Perezone Angelate as Potential Anti-Glioblastoma Multiforme Agents
title In Vitro and Computational Studies of Perezone and Perezone Angelate as Potential Anti-Glioblastoma Multiforme Agents
title_full In Vitro and Computational Studies of Perezone and Perezone Angelate as Potential Anti-Glioblastoma Multiforme Agents
title_fullStr In Vitro and Computational Studies of Perezone and Perezone Angelate as Potential Anti-Glioblastoma Multiforme Agents
title_full_unstemmed In Vitro and Computational Studies of Perezone and Perezone Angelate as Potential Anti-Glioblastoma Multiforme Agents
title_short In Vitro and Computational Studies of Perezone and Perezone Angelate as Potential Anti-Glioblastoma Multiforme Agents
title_sort in vitro and computational studies of perezone and perezone angelate as potential anti-glioblastoma multiforme agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911992/
https://www.ncbi.nlm.nih.gov/pubmed/35268667
http://dx.doi.org/10.3390/molecules27051565
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