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Synthesis of New Boron Derived Compounds; Anticancer, Antioxidant and Antimicrobial Effect in Vitro Glioblastoma Tumor Model

OBJECTIVE: The aim of our study is to investigate the cytotoxic, antioxidant, and antimicrobial effects of newly synthesized boron compounds in U87MG glioblastoma cell treatment. METHODS: We synthesized boron glycine monoester (BGM) and boron glycine diester (BGD) structures containing boron atoms a...

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Autores principales: Koldemir-Gündüz, Meliha, Aydin, Hasan Emre, Berikten, Derya, Kaymak, Güllü, Köse, Dursun Ali, Arslantaş, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurosurgical Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590914/
https://www.ncbi.nlm.nih.gov/pubmed/34571588
http://dx.doi.org/10.3340/jkns.2021.0032
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author Koldemir-Gündüz, Meliha
Aydin, Hasan Emre
Berikten, Derya
Kaymak, Güllü
Köse, Dursun Ali
Arslantaş, Ali
author_facet Koldemir-Gündüz, Meliha
Aydin, Hasan Emre
Berikten, Derya
Kaymak, Güllü
Köse, Dursun Ali
Arslantaş, Ali
author_sort Koldemir-Gündüz, Meliha
collection PubMed
description OBJECTIVE: The aim of our study is to investigate the cytotoxic, antioxidant, and antimicrobial effects of newly synthesized boron compounds in U87MG glioblastoma cell treatment. METHODS: We synthesized boron glycine monoester (BGM) and boron glycine diester (BGD) structures containing boron atoms and determined their cytotoxic activities on glioblastoma by the MTT method. The inhibitory concentration 50 (IC(50)) value was calculated with GraphPad Prism 5.0 program. The IC(50) values were administered 48 hours on U87MG glioblastoma cell. Catalase (CAT), acid phosphatase (ACP) and alkaline phosphatase (ALP) enzyme activity, malondialdehyde (MDA), total glutathione (GSH), and total protein levels were detected using spectrophotometric methods. We determined the antimicrobial activities of BGM and BGD with the disc diffusion method. RESULTS: After 48 hours of BGM and BGD application to U87MG glioblastoma cells, we found the IC(50) value as 6.6 mM and 26 mM, respectively. CAT and ACP enzyme activities were decreased in BGM and BGD groups. MDA which is a metabolite of lipid peroxidation was increased in both boron compounds groups. GSH level was reduced especially in BGD group. BGM and BGD have been found to be antimicrobial effects. CONCLUSION: Boron compounds, especially the BGM, can provide a new therapeutic approach for the treatment of glioblastoma with their anticancer, antioxidant, and antimicrobial effects.
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spelling pubmed-85909142021-11-18 Synthesis of New Boron Derived Compounds; Anticancer, Antioxidant and Antimicrobial Effect in Vitro Glioblastoma Tumor Model Koldemir-Gündüz, Meliha Aydin, Hasan Emre Berikten, Derya Kaymak, Güllü Köse, Dursun Ali Arslantaş, Ali J Korean Neurosurg Soc Laboratory Investigation OBJECTIVE: The aim of our study is to investigate the cytotoxic, antioxidant, and antimicrobial effects of newly synthesized boron compounds in U87MG glioblastoma cell treatment. METHODS: We synthesized boron glycine monoester (BGM) and boron glycine diester (BGD) structures containing boron atoms and determined their cytotoxic activities on glioblastoma by the MTT method. The inhibitory concentration 50 (IC(50)) value was calculated with GraphPad Prism 5.0 program. The IC(50) values were administered 48 hours on U87MG glioblastoma cell. Catalase (CAT), acid phosphatase (ACP) and alkaline phosphatase (ALP) enzyme activity, malondialdehyde (MDA), total glutathione (GSH), and total protein levels were detected using spectrophotometric methods. We determined the antimicrobial activities of BGM and BGD with the disc diffusion method. RESULTS: After 48 hours of BGM and BGD application to U87MG glioblastoma cells, we found the IC(50) value as 6.6 mM and 26 mM, respectively. CAT and ACP enzyme activities were decreased in BGM and BGD groups. MDA which is a metabolite of lipid peroxidation was increased in both boron compounds groups. GSH level was reduced especially in BGD group. BGM and BGD have been found to be antimicrobial effects. CONCLUSION: Boron compounds, especially the BGM, can provide a new therapeutic approach for the treatment of glioblastoma with their anticancer, antioxidant, and antimicrobial effects. Korean Neurosurgical Society 2021-11 2021-09-28 /pmc/articles/PMC8590914/ /pubmed/34571588 http://dx.doi.org/10.3340/jkns.2021.0032 Text en Copyright © 2021 The Korean Neurosurgical Society https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Laboratory Investigation
Koldemir-Gündüz, Meliha
Aydin, Hasan Emre
Berikten, Derya
Kaymak, Güllü
Köse, Dursun Ali
Arslantaş, Ali
Synthesis of New Boron Derived Compounds; Anticancer, Antioxidant and Antimicrobial Effect in Vitro Glioblastoma Tumor Model
title Synthesis of New Boron Derived Compounds; Anticancer, Antioxidant and Antimicrobial Effect in Vitro Glioblastoma Tumor Model
title_full Synthesis of New Boron Derived Compounds; Anticancer, Antioxidant and Antimicrobial Effect in Vitro Glioblastoma Tumor Model
title_fullStr Synthesis of New Boron Derived Compounds; Anticancer, Antioxidant and Antimicrobial Effect in Vitro Glioblastoma Tumor Model
title_full_unstemmed Synthesis of New Boron Derived Compounds; Anticancer, Antioxidant and Antimicrobial Effect in Vitro Glioblastoma Tumor Model
title_short Synthesis of New Boron Derived Compounds; Anticancer, Antioxidant and Antimicrobial Effect in Vitro Glioblastoma Tumor Model
title_sort synthesis of new boron derived compounds; anticancer, antioxidant and antimicrobial effect in vitro glioblastoma tumor model
topic Laboratory Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590914/
https://www.ncbi.nlm.nih.gov/pubmed/34571588
http://dx.doi.org/10.3340/jkns.2021.0032
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