Cargando…

Bee Venom Effect on Glioblastoma Cells Viability and Gelatinase Secretion

BACKGROUND: The involvement of MMP-2 and MMP-9 in the pathogenesis of various kinds of cancers including glioblastoma is well documented. The evaluation of the anticancer potential of honey bee (Apis mellifera) venom (BV) consisting of the inhibition of MMP-2 and MMP-9 secretion in a glioblastoma ce...

Descripción completa

Detalles Bibliográficos
Autores principales: Małek, Agata, Kocot, Joanna, Mitrowska, Kamila, Posyniak, Andrzej, Kurzepa, Jacek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873382/
https://www.ncbi.nlm.nih.gov/pubmed/35221898
http://dx.doi.org/10.3389/fnins.2022.792970
_version_ 1784657452856246272
author Małek, Agata
Kocot, Joanna
Mitrowska, Kamila
Posyniak, Andrzej
Kurzepa, Jacek
author_facet Małek, Agata
Kocot, Joanna
Mitrowska, Kamila
Posyniak, Andrzej
Kurzepa, Jacek
author_sort Małek, Agata
collection PubMed
description BACKGROUND: The involvement of MMP-2 and MMP-9 in the pathogenesis of various kinds of cancers including glioblastoma is well documented. The evaluation of the anticancer potential of honey bee (Apis mellifera) venom (BV) consisting of the inhibition of MMP-2 and MMP-9 secretion in a glioblastoma cell culture model was the aim of the study. METHODS: 8-MG-BA and GAMG human primary glioblastoma cell lines vs. HT-22 mouse hippocampal neuronal cells were applied for the study. The BV dose (0.5, 1.0, 1.25, 1.5, 1.75, 2.0, 2.5, and 5.0 μg/ml) and time-dependent (24, 48, 72 h) cytotoxicity was evaluated with the tetrazolium-based colorimetric assay (MTT test). MMP-2 and MMP-9 activities in the cell culture medium under different BV concentrations were determined by gelatin zymography. RESULTS: A dose and time-dependent BV effect on cytotoxicity of both glioblastoma cell lines and hippocampus line was observed. The weakest, but statistically important effect was exerted by BV on HT-22 cells. The greatest cytotoxic effect of BV was observed on the 8-MG-BA line, where a statistically significant reduction in viability was observed at the lowest BV dose and the shortest incubation time. The reduction of both gelatinases secretion was observed at 8-MG-BA and GAMG lines without significant effect of HT-22 cell line. CONCLUSION: In vitro studies indicate that BV has both cytotoxic and inhibitory effects on the secretion of MMP-2 and MMP-9 in selected lines of glioma, suggesting anticancer properties of BV.
format Online
Article
Text
id pubmed-8873382
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-88733822022-02-26 Bee Venom Effect on Glioblastoma Cells Viability and Gelatinase Secretion Małek, Agata Kocot, Joanna Mitrowska, Kamila Posyniak, Andrzej Kurzepa, Jacek Front Neurosci Neuroscience BACKGROUND: The involvement of MMP-2 and MMP-9 in the pathogenesis of various kinds of cancers including glioblastoma is well documented. The evaluation of the anticancer potential of honey bee (Apis mellifera) venom (BV) consisting of the inhibition of MMP-2 and MMP-9 secretion in a glioblastoma cell culture model was the aim of the study. METHODS: 8-MG-BA and GAMG human primary glioblastoma cell lines vs. HT-22 mouse hippocampal neuronal cells were applied for the study. The BV dose (0.5, 1.0, 1.25, 1.5, 1.75, 2.0, 2.5, and 5.0 μg/ml) and time-dependent (24, 48, 72 h) cytotoxicity was evaluated with the tetrazolium-based colorimetric assay (MTT test). MMP-2 and MMP-9 activities in the cell culture medium under different BV concentrations were determined by gelatin zymography. RESULTS: A dose and time-dependent BV effect on cytotoxicity of both glioblastoma cell lines and hippocampus line was observed. The weakest, but statistically important effect was exerted by BV on HT-22 cells. The greatest cytotoxic effect of BV was observed on the 8-MG-BA line, where a statistically significant reduction in viability was observed at the lowest BV dose and the shortest incubation time. The reduction of both gelatinases secretion was observed at 8-MG-BA and GAMG lines without significant effect of HT-22 cell line. CONCLUSION: In vitro studies indicate that BV has both cytotoxic and inhibitory effects on the secretion of MMP-2 and MMP-9 in selected lines of glioma, suggesting anticancer properties of BV. Frontiers Media S.A. 2022-02-11 /pmc/articles/PMC8873382/ /pubmed/35221898 http://dx.doi.org/10.3389/fnins.2022.792970 Text en Copyright © 2022 Małek, Kocot, Mitrowska, Posyniak and Kurzepa. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Małek, Agata
Kocot, Joanna
Mitrowska, Kamila
Posyniak, Andrzej
Kurzepa, Jacek
Bee Venom Effect on Glioblastoma Cells Viability and Gelatinase Secretion
title Bee Venom Effect on Glioblastoma Cells Viability and Gelatinase Secretion
title_full Bee Venom Effect on Glioblastoma Cells Viability and Gelatinase Secretion
title_fullStr Bee Venom Effect on Glioblastoma Cells Viability and Gelatinase Secretion
title_full_unstemmed Bee Venom Effect on Glioblastoma Cells Viability and Gelatinase Secretion
title_short Bee Venom Effect on Glioblastoma Cells Viability and Gelatinase Secretion
title_sort bee venom effect on glioblastoma cells viability and gelatinase secretion
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873382/
https://www.ncbi.nlm.nih.gov/pubmed/35221898
http://dx.doi.org/10.3389/fnins.2022.792970
work_keys_str_mv AT małekagata beevenomeffectonglioblastomacellsviabilityandgelatinasesecretion
AT kocotjoanna beevenomeffectonglioblastomacellsviabilityandgelatinasesecretion
AT mitrowskakamila beevenomeffectonglioblastomacellsviabilityandgelatinasesecretion
AT posyniakandrzej beevenomeffectonglioblastomacellsviabilityandgelatinasesecretion
AT kurzepajacek beevenomeffectonglioblastomacellsviabilityandgelatinasesecretion