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Constituents of Propolis: Chrysin, Caffeic Acid, p-Coumaric Acid, and Ferulic Acid Induce PRODH/POX-Dependent Apoptosis in Human Tongue Squamous Cell Carcinoma Cell (CAL-27)

Propolis evokes several therapeutic properties, including anticancer activity. These activities are attributed to the action of polyphenols. Previously it has been demonstrated, that one of the most abundant polyphenolic compounds in ethanolic extracts of propolis are chrysin, caffeic acid, p-coumar...

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Autores principales: Celińska-Janowicz, Katarzyna, Zaręba, Ilona, Lazarek, Urszula, Teul, Joanna, Tomczyk, Michał, Pałka, Jerzy, Miltyk, Wojciech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897514/
https://www.ncbi.nlm.nih.gov/pubmed/29681859
http://dx.doi.org/10.3389/fphar.2018.00336
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author Celińska-Janowicz, Katarzyna
Zaręba, Ilona
Lazarek, Urszula
Teul, Joanna
Tomczyk, Michał
Pałka, Jerzy
Miltyk, Wojciech
author_facet Celińska-Janowicz, Katarzyna
Zaręba, Ilona
Lazarek, Urszula
Teul, Joanna
Tomczyk, Michał
Pałka, Jerzy
Miltyk, Wojciech
author_sort Celińska-Janowicz, Katarzyna
collection PubMed
description Propolis evokes several therapeutic properties, including anticancer activity. These activities are attributed to the action of polyphenols. Previously it has been demonstrated, that one of the most abundant polyphenolic compounds in ethanolic extracts of propolis are chrysin, caffeic acid, p-coumaric acid, and ferulic acid. Although their pro-apoptotic activity on human tongue squamous cell carcinoma cells (CAL-27) was established previously, the detailed mechanism of this process remains unclear. Considering the crucial role of proline metabolism and proline dehydrogenase/proline oxidase (PRODH/POX) in the regulation of cancer cell survival/apoptosis, we studied these processes in polyphenol-treated CAL-27 cells. All studied polyphenols evoked anti-proliferative activity, accompanied by increased PRODH/POX, P53, active caspases-3 and -9 expressions and decreased collagen biosynthesis, prolidase activity and proline concentration in CAL-27 cells. These data suggest that polyphenols of propolis induce PRODH/POX-dependent apoptosis through up-regulation of mitochondrial proline degradation and down-regulation of proline utilization for collagen biosynthesis.
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spelling pubmed-58975142018-04-20 Constituents of Propolis: Chrysin, Caffeic Acid, p-Coumaric Acid, and Ferulic Acid Induce PRODH/POX-Dependent Apoptosis in Human Tongue Squamous Cell Carcinoma Cell (CAL-27) Celińska-Janowicz, Katarzyna Zaręba, Ilona Lazarek, Urszula Teul, Joanna Tomczyk, Michał Pałka, Jerzy Miltyk, Wojciech Front Pharmacol Pharmacology Propolis evokes several therapeutic properties, including anticancer activity. These activities are attributed to the action of polyphenols. Previously it has been demonstrated, that one of the most abundant polyphenolic compounds in ethanolic extracts of propolis are chrysin, caffeic acid, p-coumaric acid, and ferulic acid. Although their pro-apoptotic activity on human tongue squamous cell carcinoma cells (CAL-27) was established previously, the detailed mechanism of this process remains unclear. Considering the crucial role of proline metabolism and proline dehydrogenase/proline oxidase (PRODH/POX) in the regulation of cancer cell survival/apoptosis, we studied these processes in polyphenol-treated CAL-27 cells. All studied polyphenols evoked anti-proliferative activity, accompanied by increased PRODH/POX, P53, active caspases-3 and -9 expressions and decreased collagen biosynthesis, prolidase activity and proline concentration in CAL-27 cells. These data suggest that polyphenols of propolis induce PRODH/POX-dependent apoptosis through up-regulation of mitochondrial proline degradation and down-regulation of proline utilization for collagen biosynthesis. Frontiers Media S.A. 2018-04-06 /pmc/articles/PMC5897514/ /pubmed/29681859 http://dx.doi.org/10.3389/fphar.2018.00336 Text en Copyright © 2018 Celińska-Janowicz, Zaręba, Lazarek, Teul, Tomczyk, Pałka and Miltyk. http://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 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 Pharmacology
Celińska-Janowicz, Katarzyna
Zaręba, Ilona
Lazarek, Urszula
Teul, Joanna
Tomczyk, Michał
Pałka, Jerzy
Miltyk, Wojciech
Constituents of Propolis: Chrysin, Caffeic Acid, p-Coumaric Acid, and Ferulic Acid Induce PRODH/POX-Dependent Apoptosis in Human Tongue Squamous Cell Carcinoma Cell (CAL-27)
title Constituents of Propolis: Chrysin, Caffeic Acid, p-Coumaric Acid, and Ferulic Acid Induce PRODH/POX-Dependent Apoptosis in Human Tongue Squamous Cell Carcinoma Cell (CAL-27)
title_full Constituents of Propolis: Chrysin, Caffeic Acid, p-Coumaric Acid, and Ferulic Acid Induce PRODH/POX-Dependent Apoptosis in Human Tongue Squamous Cell Carcinoma Cell (CAL-27)
title_fullStr Constituents of Propolis: Chrysin, Caffeic Acid, p-Coumaric Acid, and Ferulic Acid Induce PRODH/POX-Dependent Apoptosis in Human Tongue Squamous Cell Carcinoma Cell (CAL-27)
title_full_unstemmed Constituents of Propolis: Chrysin, Caffeic Acid, p-Coumaric Acid, and Ferulic Acid Induce PRODH/POX-Dependent Apoptosis in Human Tongue Squamous Cell Carcinoma Cell (CAL-27)
title_short Constituents of Propolis: Chrysin, Caffeic Acid, p-Coumaric Acid, and Ferulic Acid Induce PRODH/POX-Dependent Apoptosis in Human Tongue Squamous Cell Carcinoma Cell (CAL-27)
title_sort constituents of propolis: chrysin, caffeic acid, p-coumaric acid, and ferulic acid induce prodh/pox-dependent apoptosis in human tongue squamous cell carcinoma cell (cal-27)
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897514/
https://www.ncbi.nlm.nih.gov/pubmed/29681859
http://dx.doi.org/10.3389/fphar.2018.00336
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