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Polish and New Zealand Propolis as Sources of Antioxidant Compounds Inhibit Glioblastoma (T98G, LN-18) Cell Lines and Astrocytoma Cells Derived from Patient

Gliomas, including glioblastoma multiforme and astrocytoma, are common brain cancers in adults. Propolis is a natural product containing many active ingredients. The aim of this study was to compare the chemical composition, total phenolic content and concentration of toxic elements as well as the a...

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Autores principales: Moskwa, Justyna, Naliwajko, Sylwia Katarzyna, Markiewicz-Żukowska, Renata, Gromkowska-Kępka, Krystyna Joanna, Soroczyńska, Jolanta, Puścion-Jakubik, Anna, Borawska, Maria Halina, Isidorov, Valery, Socha, Katarzyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9312157/
https://www.ncbi.nlm.nih.gov/pubmed/35883797
http://dx.doi.org/10.3390/antiox11071305
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author Moskwa, Justyna
Naliwajko, Sylwia Katarzyna
Markiewicz-Żukowska, Renata
Gromkowska-Kępka, Krystyna Joanna
Soroczyńska, Jolanta
Puścion-Jakubik, Anna
Borawska, Maria Halina
Isidorov, Valery
Socha, Katarzyna
author_facet Moskwa, Justyna
Naliwajko, Sylwia Katarzyna
Markiewicz-Żukowska, Renata
Gromkowska-Kępka, Krystyna Joanna
Soroczyńska, Jolanta
Puścion-Jakubik, Anna
Borawska, Maria Halina
Isidorov, Valery
Socha, Katarzyna
author_sort Moskwa, Justyna
collection PubMed
description Gliomas, including glioblastoma multiforme and astrocytoma, are common brain cancers in adults. Propolis is a natural product containing many active ingredients. The aim of this study was to compare the chemical composition, total phenolic content and concentration of toxic elements as well as the anticancer potential of Polish (PPE) and New Zealand (Manuka—MPE) propolis extracts on diffuse astrocytoma derived from patient (DASC) and glioblastoma (T98G, LN-18) cell lines. The antioxidants such as flavonoids and chalcones (pinocembrin, pinobanksin, pinobanksin 3-acetate and chrysin) were the main components in both types of propolis. The content of arsenic (As) and lead (Pb) in MPE was higher than PPE. The anti-proliferative study showed strong activity of PPE and MPE propolis on DASC, T98G, and LN-18 cells by apoptosis induction, cell cycle arrest and attenuated migration. These findings suggest that despite their different geographic origins, Polish and New Zealand propolis are sources of antioxidant compounds and show similar activity and a promising anti-glioma potential in in vitro study. However, further in vivo studies are required in order to assess therapeutic potential of propolis.
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spelling pubmed-93121572022-07-26 Polish and New Zealand Propolis as Sources of Antioxidant Compounds Inhibit Glioblastoma (T98G, LN-18) Cell Lines and Astrocytoma Cells Derived from Patient Moskwa, Justyna Naliwajko, Sylwia Katarzyna Markiewicz-Żukowska, Renata Gromkowska-Kępka, Krystyna Joanna Soroczyńska, Jolanta Puścion-Jakubik, Anna Borawska, Maria Halina Isidorov, Valery Socha, Katarzyna Antioxidants (Basel) Article Gliomas, including glioblastoma multiforme and astrocytoma, are common brain cancers in adults. Propolis is a natural product containing many active ingredients. The aim of this study was to compare the chemical composition, total phenolic content and concentration of toxic elements as well as the anticancer potential of Polish (PPE) and New Zealand (Manuka—MPE) propolis extracts on diffuse astrocytoma derived from patient (DASC) and glioblastoma (T98G, LN-18) cell lines. The antioxidants such as flavonoids and chalcones (pinocembrin, pinobanksin, pinobanksin 3-acetate and chrysin) were the main components in both types of propolis. The content of arsenic (As) and lead (Pb) in MPE was higher than PPE. The anti-proliferative study showed strong activity of PPE and MPE propolis on DASC, T98G, and LN-18 cells by apoptosis induction, cell cycle arrest and attenuated migration. These findings suggest that despite their different geographic origins, Polish and New Zealand propolis are sources of antioxidant compounds and show similar activity and a promising anti-glioma potential in in vitro study. However, further in vivo studies are required in order to assess therapeutic potential of propolis. MDPI 2022-06-29 /pmc/articles/PMC9312157/ /pubmed/35883797 http://dx.doi.org/10.3390/antiox11071305 Text en © 2022 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
Moskwa, Justyna
Naliwajko, Sylwia Katarzyna
Markiewicz-Żukowska, Renata
Gromkowska-Kępka, Krystyna Joanna
Soroczyńska, Jolanta
Puścion-Jakubik, Anna
Borawska, Maria Halina
Isidorov, Valery
Socha, Katarzyna
Polish and New Zealand Propolis as Sources of Antioxidant Compounds Inhibit Glioblastoma (T98G, LN-18) Cell Lines and Astrocytoma Cells Derived from Patient
title Polish and New Zealand Propolis as Sources of Antioxidant Compounds Inhibit Glioblastoma (T98G, LN-18) Cell Lines and Astrocytoma Cells Derived from Patient
title_full Polish and New Zealand Propolis as Sources of Antioxidant Compounds Inhibit Glioblastoma (T98G, LN-18) Cell Lines and Astrocytoma Cells Derived from Patient
title_fullStr Polish and New Zealand Propolis as Sources of Antioxidant Compounds Inhibit Glioblastoma (T98G, LN-18) Cell Lines and Astrocytoma Cells Derived from Patient
title_full_unstemmed Polish and New Zealand Propolis as Sources of Antioxidant Compounds Inhibit Glioblastoma (T98G, LN-18) Cell Lines and Astrocytoma Cells Derived from Patient
title_short Polish and New Zealand Propolis as Sources of Antioxidant Compounds Inhibit Glioblastoma (T98G, LN-18) Cell Lines and Astrocytoma Cells Derived from Patient
title_sort polish and new zealand propolis as sources of antioxidant compounds inhibit glioblastoma (t98g, ln-18) cell lines and astrocytoma cells derived from patient
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9312157/
https://www.ncbi.nlm.nih.gov/pubmed/35883797
http://dx.doi.org/10.3390/antiox11071305
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