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Melatonin in Combination with Albendazole or Albendazole Sulfoxide Produces a Synergistic Cytotoxicity against Malignant Glioma Cells through Autophagy and Apoptosis

Glioblastoma is the most aggressive and lethal brain tumor in adults, presenting diffuse brain infiltration, necrosis, and drug resistance. Although new drugs have been approved for recurrent patients, the median survival rate is two years; therefore, new alternatives to treat these patients are req...

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Autores principales: Hernández-Cerón, Miguel, Chavarria, Víctor, Ríos, Camilo, Pineda, Benjamin, Palomares-Alonso, Francisca, Rojas-Tomé, Irma Susana, Jung-Cook, Helgi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295958/
https://www.ncbi.nlm.nih.gov/pubmed/37371349
http://dx.doi.org/10.3390/brainsci13060869
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author Hernández-Cerón, Miguel
Chavarria, Víctor
Ríos, Camilo
Pineda, Benjamin
Palomares-Alonso, Francisca
Rojas-Tomé, Irma Susana
Jung-Cook, Helgi
author_facet Hernández-Cerón, Miguel
Chavarria, Víctor
Ríos, Camilo
Pineda, Benjamin
Palomares-Alonso, Francisca
Rojas-Tomé, Irma Susana
Jung-Cook, Helgi
author_sort Hernández-Cerón, Miguel
collection PubMed
description Glioblastoma is the most aggressive and lethal brain tumor in adults, presenting diffuse brain infiltration, necrosis, and drug resistance. Although new drugs have been approved for recurrent patients, the median survival rate is two years; therefore, new alternatives to treat these patients are required. Previous studies have reported the anticancer activity of albendazole, its active metabolite albendazole sulfoxide, and melatonin; therefore, the present study was performed to evaluate if the combination of melatonin with albendazole or with albendazole sulfoxide induces an additive or synergistic cytotoxic effect on C6 and RG2 rat glioma cells, as well as on U87 human glioblastoma cells. Drug interaction was determined by the Chou–Talalay method. We evaluated the mechanism of cell death by flow cytometry, immunofluorescence, and crystal violet staining. The cytotoxicity of the combinations was mainly synergistic. The combined treatments induced significantly more apoptotic and autophagic cell death on the glioma cell lines. Additionally, albendazole and albendazole sulfoxide inhibited proliferation independently of melatonin. Our data justify continuing with the evaluation of this proposal since the combinations could be a potential strategy to aid in the treatment of glioblastoma.
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spelling pubmed-102959582023-06-28 Melatonin in Combination with Albendazole or Albendazole Sulfoxide Produces a Synergistic Cytotoxicity against Malignant Glioma Cells through Autophagy and Apoptosis Hernández-Cerón, Miguel Chavarria, Víctor Ríos, Camilo Pineda, Benjamin Palomares-Alonso, Francisca Rojas-Tomé, Irma Susana Jung-Cook, Helgi Brain Sci Article Glioblastoma is the most aggressive and lethal brain tumor in adults, presenting diffuse brain infiltration, necrosis, and drug resistance. Although new drugs have been approved for recurrent patients, the median survival rate is two years; therefore, new alternatives to treat these patients are required. Previous studies have reported the anticancer activity of albendazole, its active metabolite albendazole sulfoxide, and melatonin; therefore, the present study was performed to evaluate if the combination of melatonin with albendazole or with albendazole sulfoxide induces an additive or synergistic cytotoxic effect on C6 and RG2 rat glioma cells, as well as on U87 human glioblastoma cells. Drug interaction was determined by the Chou–Talalay method. We evaluated the mechanism of cell death by flow cytometry, immunofluorescence, and crystal violet staining. The cytotoxicity of the combinations was mainly synergistic. The combined treatments induced significantly more apoptotic and autophagic cell death on the glioma cell lines. Additionally, albendazole and albendazole sulfoxide inhibited proliferation independently of melatonin. Our data justify continuing with the evaluation of this proposal since the combinations could be a potential strategy to aid in the treatment of glioblastoma. MDPI 2023-05-27 /pmc/articles/PMC10295958/ /pubmed/37371349 http://dx.doi.org/10.3390/brainsci13060869 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
Hernández-Cerón, Miguel
Chavarria, Víctor
Ríos, Camilo
Pineda, Benjamin
Palomares-Alonso, Francisca
Rojas-Tomé, Irma Susana
Jung-Cook, Helgi
Melatonin in Combination with Albendazole or Albendazole Sulfoxide Produces a Synergistic Cytotoxicity against Malignant Glioma Cells through Autophagy and Apoptosis
title Melatonin in Combination with Albendazole or Albendazole Sulfoxide Produces a Synergistic Cytotoxicity against Malignant Glioma Cells through Autophagy and Apoptosis
title_full Melatonin in Combination with Albendazole or Albendazole Sulfoxide Produces a Synergistic Cytotoxicity against Malignant Glioma Cells through Autophagy and Apoptosis
title_fullStr Melatonin in Combination with Albendazole or Albendazole Sulfoxide Produces a Synergistic Cytotoxicity against Malignant Glioma Cells through Autophagy and Apoptosis
title_full_unstemmed Melatonin in Combination with Albendazole or Albendazole Sulfoxide Produces a Synergistic Cytotoxicity against Malignant Glioma Cells through Autophagy and Apoptosis
title_short Melatonin in Combination with Albendazole or Albendazole Sulfoxide Produces a Synergistic Cytotoxicity against Malignant Glioma Cells through Autophagy and Apoptosis
title_sort melatonin in combination with albendazole or albendazole sulfoxide produces a synergistic cytotoxicity against malignant glioma cells through autophagy and apoptosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10295958/
https://www.ncbi.nlm.nih.gov/pubmed/37371349
http://dx.doi.org/10.3390/brainsci13060869
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