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Emodin-8-O-Glucoside—Isolation and the Screening of the Anticancer Potential against the Nervous System Tumors

Emodin-8-O-glucoside (E-8-O-G) is a glycosylated derivative of emodin that exhibits numerous biological activities, including immunomodulatory, anti-inflammatory, antioxidant, hepatoprotective, or anticancer activities. However, there are no reports on the activity of E-8-O-G against cancers of the...

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Autores principales: Okon, Estera, Koval, Maryna, Wawruszak, Anna, Slawinska-Brych, Adrianna, Smolinska, Katarzyna, Shevera, Myroslav, Stepulak, Andrzej, Kukula-Koch, Wirginia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650745/
https://www.ncbi.nlm.nih.gov/pubmed/37959784
http://dx.doi.org/10.3390/molecules28217366
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author Okon, Estera
Koval, Maryna
Wawruszak, Anna
Slawinska-Brych, Adrianna
Smolinska, Katarzyna
Shevera, Myroslav
Stepulak, Andrzej
Kukula-Koch, Wirginia
author_facet Okon, Estera
Koval, Maryna
Wawruszak, Anna
Slawinska-Brych, Adrianna
Smolinska, Katarzyna
Shevera, Myroslav
Stepulak, Andrzej
Kukula-Koch, Wirginia
author_sort Okon, Estera
collection PubMed
description Emodin-8-O-glucoside (E-8-O-G) is a glycosylated derivative of emodin that exhibits numerous biological activities, including immunomodulatory, anti-inflammatory, antioxidant, hepatoprotective, or anticancer activities. However, there are no reports on the activity of E-8-O-G against cancers of the nervous system. Therefore, the aim of the study was to investigate the antiproliferative and cytotoxic effect of E-8-O-G in the SK-N-AS neuroblastoma, T98G human glioblastoma, and C6 mouse glioblastoma cancer cells. As a source of E-8-O-G the methanolic extract from the aerial parts of Reynoutria japonica Houtt. (Polygonaceae) was used. Thanks to the application of centrifugal partition chromatography (CPC) operated in the descending mode using a mixture of petroleum ether:ethyl acetate:methanol:water (4:5:4:5 v/v/v/v) and a subsequent purification with preparative HPLC, E-8-O-G was obtained in high purity in a sufficient quantity for the bioactivity tests. Assessment of the cancer cell viability and proliferation were performed with the MTT (3-(bromide 4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium), CTG (CellTiter-Glo(®)) and BrdU (5-bromo-2′-deoxyuridine) assays, respectively. E-8-O-G inhibits the viability and proliferation of SK-N-AS neuroblastoma, T98G human glioblastoma multiforme, and C6 mouse glioblastoma cells dose-dependently. E-8-O-G seems to be a promising natural antitumor compound in the therapy of nervous system tumors.
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spelling pubmed-106507452023-10-31 Emodin-8-O-Glucoside—Isolation and the Screening of the Anticancer Potential against the Nervous System Tumors Okon, Estera Koval, Maryna Wawruszak, Anna Slawinska-Brych, Adrianna Smolinska, Katarzyna Shevera, Myroslav Stepulak, Andrzej Kukula-Koch, Wirginia Molecules Article Emodin-8-O-glucoside (E-8-O-G) is a glycosylated derivative of emodin that exhibits numerous biological activities, including immunomodulatory, anti-inflammatory, antioxidant, hepatoprotective, or anticancer activities. However, there are no reports on the activity of E-8-O-G against cancers of the nervous system. Therefore, the aim of the study was to investigate the antiproliferative and cytotoxic effect of E-8-O-G in the SK-N-AS neuroblastoma, T98G human glioblastoma, and C6 mouse glioblastoma cancer cells. As a source of E-8-O-G the methanolic extract from the aerial parts of Reynoutria japonica Houtt. (Polygonaceae) was used. Thanks to the application of centrifugal partition chromatography (CPC) operated in the descending mode using a mixture of petroleum ether:ethyl acetate:methanol:water (4:5:4:5 v/v/v/v) and a subsequent purification with preparative HPLC, E-8-O-G was obtained in high purity in a sufficient quantity for the bioactivity tests. Assessment of the cancer cell viability and proliferation were performed with the MTT (3-(bromide 4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium), CTG (CellTiter-Glo(®)) and BrdU (5-bromo-2′-deoxyuridine) assays, respectively. E-8-O-G inhibits the viability and proliferation of SK-N-AS neuroblastoma, T98G human glioblastoma multiforme, and C6 mouse glioblastoma cells dose-dependently. E-8-O-G seems to be a promising natural antitumor compound in the therapy of nervous system tumors. MDPI 2023-10-31 /pmc/articles/PMC10650745/ /pubmed/37959784 http://dx.doi.org/10.3390/molecules28217366 Text en © 2023 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
Okon, Estera
Koval, Maryna
Wawruszak, Anna
Slawinska-Brych, Adrianna
Smolinska, Katarzyna
Shevera, Myroslav
Stepulak, Andrzej
Kukula-Koch, Wirginia
Emodin-8-O-Glucoside—Isolation and the Screening of the Anticancer Potential against the Nervous System Tumors
title Emodin-8-O-Glucoside—Isolation and the Screening of the Anticancer Potential against the Nervous System Tumors
title_full Emodin-8-O-Glucoside—Isolation and the Screening of the Anticancer Potential against the Nervous System Tumors
title_fullStr Emodin-8-O-Glucoside—Isolation and the Screening of the Anticancer Potential against the Nervous System Tumors
title_full_unstemmed Emodin-8-O-Glucoside—Isolation and the Screening of the Anticancer Potential against the Nervous System Tumors
title_short Emodin-8-O-Glucoside—Isolation and the Screening of the Anticancer Potential against the Nervous System Tumors
title_sort emodin-8-o-glucoside—isolation and the screening of the anticancer potential against the nervous system tumors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650745/
https://www.ncbi.nlm.nih.gov/pubmed/37959784
http://dx.doi.org/10.3390/molecules28217366
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