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Differential Apoptotic Effects of Bee Product Mixtures on Normal and Cancer Hepatic Cells

Most effective anticancer drugs normally generate considerable cytotoxicity in normal cells; therefore, the preferential activation of apoptosis in cancer cells and the reduction of toxicity in normal cells is a great challenge in cancer research. Natural products with selective anticancer propertie...

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Autores principales: Sánchez-Martín, Vanesa, Morales, Paloma, Iriondo-DeHond, Amaia, Hospital, Xavier F., Fernández, Manuela, Hierro, Eva, Haza, Ana I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045410/
https://www.ncbi.nlm.nih.gov/pubmed/36978864
http://dx.doi.org/10.3390/antiox12030615
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author Sánchez-Martín, Vanesa
Morales, Paloma
Iriondo-DeHond, Amaia
Hospital, Xavier F.
Fernández, Manuela
Hierro, Eva
Haza, Ana I.
author_facet Sánchez-Martín, Vanesa
Morales, Paloma
Iriondo-DeHond, Amaia
Hospital, Xavier F.
Fernández, Manuela
Hierro, Eva
Haza, Ana I.
author_sort Sánchez-Martín, Vanesa
collection PubMed
description Most effective anticancer drugs normally generate considerable cytotoxicity in normal cells; therefore, the preferential activation of apoptosis in cancer cells and the reduction of toxicity in normal cells is a great challenge in cancer research. Natural products with selective anticancer properties used as complementary medicine can help to achieve this goal. The aim of the present study was to analyze the effect of the addition of bee products [propolis (PR) or royal jelly (RJ) or propolis and royal jelly (PR+RJ), 2–10%] to thyme (TH) and chestnut honeys (CH) on the differential anticancer properties, mainly the cytotoxic and pro-apoptotic effects, in normal and cancer hepatic cells. The cytotoxic effects of samples were analyzed using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay (0–250 mg/mL) and the effects on apoptosis were analyzed using cell cycle analysis, TdT-dUTP terminal nick-end labeling (TUNEL) assay, DR5 (Death Receptor 5) and BAX (BCL-2-Associated X) activation, and caspases 8, 9, and 3 activities. Both honey samples alone and honey mixtures had no or very little apoptotic effect on normal cells. Antioxidant honey mixtures enhanced the apoptotic capacity of the corresponding honey alone via both extrinsic and intrinsic pathways. Of all the samples, chestnut honey enriched with 10% royal jelly and 10% propolis (sample 14, CH+10RJ+10PR) showed the highest apoptotic effect on tumor liver cells. The enrichment of monofloral honey with bee products could be used together with conventional anticancer treatments as a dietary supplement without side effects. On the other hand, it could be included in the diet as a natural sweetener with high added value.
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spelling pubmed-100454102023-03-29 Differential Apoptotic Effects of Bee Product Mixtures on Normal and Cancer Hepatic Cells Sánchez-Martín, Vanesa Morales, Paloma Iriondo-DeHond, Amaia Hospital, Xavier F. Fernández, Manuela Hierro, Eva Haza, Ana I. Antioxidants (Basel) Article Most effective anticancer drugs normally generate considerable cytotoxicity in normal cells; therefore, the preferential activation of apoptosis in cancer cells and the reduction of toxicity in normal cells is a great challenge in cancer research. Natural products with selective anticancer properties used as complementary medicine can help to achieve this goal. The aim of the present study was to analyze the effect of the addition of bee products [propolis (PR) or royal jelly (RJ) or propolis and royal jelly (PR+RJ), 2–10%] to thyme (TH) and chestnut honeys (CH) on the differential anticancer properties, mainly the cytotoxic and pro-apoptotic effects, in normal and cancer hepatic cells. The cytotoxic effects of samples were analyzed using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay (0–250 mg/mL) and the effects on apoptosis were analyzed using cell cycle analysis, TdT-dUTP terminal nick-end labeling (TUNEL) assay, DR5 (Death Receptor 5) and BAX (BCL-2-Associated X) activation, and caspases 8, 9, and 3 activities. Both honey samples alone and honey mixtures had no or very little apoptotic effect on normal cells. Antioxidant honey mixtures enhanced the apoptotic capacity of the corresponding honey alone via both extrinsic and intrinsic pathways. Of all the samples, chestnut honey enriched with 10% royal jelly and 10% propolis (sample 14, CH+10RJ+10PR) showed the highest apoptotic effect on tumor liver cells. The enrichment of monofloral honey with bee products could be used together with conventional anticancer treatments as a dietary supplement without side effects. On the other hand, it could be included in the diet as a natural sweetener with high added value. MDPI 2023-03-02 /pmc/articles/PMC10045410/ /pubmed/36978864 http://dx.doi.org/10.3390/antiox12030615 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
Sánchez-Martín, Vanesa
Morales, Paloma
Iriondo-DeHond, Amaia
Hospital, Xavier F.
Fernández, Manuela
Hierro, Eva
Haza, Ana I.
Differential Apoptotic Effects of Bee Product Mixtures on Normal and Cancer Hepatic Cells
title Differential Apoptotic Effects of Bee Product Mixtures on Normal and Cancer Hepatic Cells
title_full Differential Apoptotic Effects of Bee Product Mixtures on Normal and Cancer Hepatic Cells
title_fullStr Differential Apoptotic Effects of Bee Product Mixtures on Normal and Cancer Hepatic Cells
title_full_unstemmed Differential Apoptotic Effects of Bee Product Mixtures on Normal and Cancer Hepatic Cells
title_short Differential Apoptotic Effects of Bee Product Mixtures on Normal and Cancer Hepatic Cells
title_sort differential apoptotic effects of bee product mixtures on normal and cancer hepatic cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045410/
https://www.ncbi.nlm.nih.gov/pubmed/36978864
http://dx.doi.org/10.3390/antiox12030615
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