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The effect of Azo-dyes on glioblastoma cells in vitro

Despite the multidisciplinary standard treatment of glioblastoma (GB) consisting of maximal surgical resection, followed by radiotherapy (RT) plus concomitant chemotherapy with temozolomide (TMZ), the majority of patients experience tumor progression and almost universal mortality. In recent years,...

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Autores principales: Sevastre, Ani-Simona, Baloi, Carina, Alexandru, Oana, Tataranu, Ligia Gabriela, Popescu, Oana Stefana, Dricu, Anica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9975690/
https://www.ncbi.nlm.nih.gov/pubmed/36874201
http://dx.doi.org/10.1016/j.sjbs.2023.103599
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author Sevastre, Ani-Simona
Baloi, Carina
Alexandru, Oana
Tataranu, Ligia Gabriela
Popescu, Oana Stefana
Dricu, Anica
author_facet Sevastre, Ani-Simona
Baloi, Carina
Alexandru, Oana
Tataranu, Ligia Gabriela
Popescu, Oana Stefana
Dricu, Anica
author_sort Sevastre, Ani-Simona
collection PubMed
description Despite the multidisciplinary standard treatment of glioblastoma (GB) consisting of maximal surgical resection, followed by radiotherapy (RT) plus concomitant chemotherapy with temozolomide (TMZ), the majority of patients experience tumor progression and almost universal mortality. In recent years, efforts have been made to create new agents for GB treatment, of which azo-dyes proved to be potential candidates, showing antiproliferative effects by inducing apoptosis and by inhibiting different signaling pathways. In this study we evaluated the antiproliferative the effect of six azo-dyes and TMZ on a low passage human GB cell line using MTT assay. We found that all compounds proved antiproliferative properties on GB cells. At equimolar concentrations azo-dyes induced more cytotoxic effect than TMZ. We found that Methyl Orange required the lowest IC(50) for 3 days of treatment (26.4684 μM), whilst for 7 days of treatment, two azo dyes proved to have the highest potency: Methyl Orange IC(50) = 13.8808 μM and Sudan I IC(50) = 12.4829 μM. The highest IC(50) was determined for TMZ under both experimental situations. Conclusions: Our research represents a novelty, by offering unique valuable data regarding the azo-dye cyototoxic effects in high grade brain tumors. This study may focus the attention on azo-dye agents that may represent an insufficient exploited source of agents for cancer treatment.
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spelling pubmed-99756902023-03-02 The effect of Azo-dyes on glioblastoma cells in vitro Sevastre, Ani-Simona Baloi, Carina Alexandru, Oana Tataranu, Ligia Gabriela Popescu, Oana Stefana Dricu, Anica Saudi J Biol Sci Original Article Despite the multidisciplinary standard treatment of glioblastoma (GB) consisting of maximal surgical resection, followed by radiotherapy (RT) plus concomitant chemotherapy with temozolomide (TMZ), the majority of patients experience tumor progression and almost universal mortality. In recent years, efforts have been made to create new agents for GB treatment, of which azo-dyes proved to be potential candidates, showing antiproliferative effects by inducing apoptosis and by inhibiting different signaling pathways. In this study we evaluated the antiproliferative the effect of six azo-dyes and TMZ on a low passage human GB cell line using MTT assay. We found that all compounds proved antiproliferative properties on GB cells. At equimolar concentrations azo-dyes induced more cytotoxic effect than TMZ. We found that Methyl Orange required the lowest IC(50) for 3 days of treatment (26.4684 μM), whilst for 7 days of treatment, two azo dyes proved to have the highest potency: Methyl Orange IC(50) = 13.8808 μM and Sudan I IC(50) = 12.4829 μM. The highest IC(50) was determined for TMZ under both experimental situations. Conclusions: Our research represents a novelty, by offering unique valuable data regarding the azo-dye cyototoxic effects in high grade brain tumors. This study may focus the attention on azo-dye agents that may represent an insufficient exploited source of agents for cancer treatment. Elsevier 2023-03 2023-02-14 /pmc/articles/PMC9975690/ /pubmed/36874201 http://dx.doi.org/10.1016/j.sjbs.2023.103599 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Sevastre, Ani-Simona
Baloi, Carina
Alexandru, Oana
Tataranu, Ligia Gabriela
Popescu, Oana Stefana
Dricu, Anica
The effect of Azo-dyes on glioblastoma cells in vitro
title The effect of Azo-dyes on glioblastoma cells in vitro
title_full The effect of Azo-dyes on glioblastoma cells in vitro
title_fullStr The effect of Azo-dyes on glioblastoma cells in vitro
title_full_unstemmed The effect of Azo-dyes on glioblastoma cells in vitro
title_short The effect of Azo-dyes on glioblastoma cells in vitro
title_sort effect of azo-dyes on glioblastoma cells in vitro
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9975690/
https://www.ncbi.nlm.nih.gov/pubmed/36874201
http://dx.doi.org/10.1016/j.sjbs.2023.103599
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