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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Neurosurgical Society
2021
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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. |
format | Online Article Text |
id | pubmed-8590914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Korean Neurosurgical Society |
record_format | MEDLINE/PubMed |
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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