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Caffeic Acid Phenethyl Ester and Ethanol Extract of Propolis Induce the Complementary Cytotoxic Effect on Triple-Negative Breast Cancer Cell Lines

Chemotherapy of breast cancer could be improved by bioactive natural substances, which may potentially sensitize the carcinoma cells’ susceptibility to drugs. Numerous phytochemicals, including propolis, have been reported to interfere with the viability of carcinoma cells. We evaluated the in vitro...

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Autores principales: Rzepecka-Stojko, Anna, Kabała-Dzik, Agata, Moździerz, Aleksandra, Kubina, Robert, Wojtyczka, Robert D., Stojko, Rafał, Dziedzic, Arkadiusz, Jastrzębska-Stojko, Żaneta, Jurzak, Magdalena, Buszman, Ewa, Stojko, Jerzy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272161/
https://www.ncbi.nlm.nih.gov/pubmed/26007182
http://dx.doi.org/10.3390/molecules20059242
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author Rzepecka-Stojko, Anna
Kabała-Dzik, Agata
Moździerz, Aleksandra
Kubina, Robert
Wojtyczka, Robert D.
Stojko, Rafał
Dziedzic, Arkadiusz
Jastrzębska-Stojko, Żaneta
Jurzak, Magdalena
Buszman, Ewa
Stojko, Jerzy
author_facet Rzepecka-Stojko, Anna
Kabała-Dzik, Agata
Moździerz, Aleksandra
Kubina, Robert
Wojtyczka, Robert D.
Stojko, Rafał
Dziedzic, Arkadiusz
Jastrzębska-Stojko, Żaneta
Jurzak, Magdalena
Buszman, Ewa
Stojko, Jerzy
author_sort Rzepecka-Stojko, Anna
collection PubMed
description Chemotherapy of breast cancer could be improved by bioactive natural substances, which may potentially sensitize the carcinoma cells’ susceptibility to drugs. Numerous phytochemicals, including propolis, have been reported to interfere with the viability of carcinoma cells. We evaluated the in vitro cytotoxic activity of ethanol extract of propolis (EEP) and its derivative caffeic acid phenethyl ester (CAPE) towards two triple-negative breast cancer (TNBC) cell lines, MDA-MB-231 and Hs578T, by implementation of the MTT and lactate dehydrogenase (LDH) assays. The morphological changes of breast carcinoma cells were observed following exposure to EEP and CAPE. The IC(50) of EEP was 48.35 µg∙mL(−1) for MDA-MB-23 cells and 33.68 µg∙mL(−1) for Hs578T cells, whereas the CAPE IC(50) was 14.08 µM and 8.01 µM for the MDA-MB-231 and Hs578T cell line, respectively. Here, we report that propolis and CAPE inhibited the growth of the MDA-MB-231 and Hs578T lines in a dose-dependent and exposure time-dependent manner. EEP showed less cytotoxic activity against both types of TNBC cells. EEP and, particularly, CAPE may markedly affect the viability of breast cancer cells, suggesting the potential role of bioactive compounds in chemoprevention/chemotherapy by potentiating the action of standard anti-cancer drugs.
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spelling pubmed-62721612019-01-07 Caffeic Acid Phenethyl Ester and Ethanol Extract of Propolis Induce the Complementary Cytotoxic Effect on Triple-Negative Breast Cancer Cell Lines Rzepecka-Stojko, Anna Kabała-Dzik, Agata Moździerz, Aleksandra Kubina, Robert Wojtyczka, Robert D. Stojko, Rafał Dziedzic, Arkadiusz Jastrzębska-Stojko, Żaneta Jurzak, Magdalena Buszman, Ewa Stojko, Jerzy Molecules Article Chemotherapy of breast cancer could be improved by bioactive natural substances, which may potentially sensitize the carcinoma cells’ susceptibility to drugs. Numerous phytochemicals, including propolis, have been reported to interfere with the viability of carcinoma cells. We evaluated the in vitro cytotoxic activity of ethanol extract of propolis (EEP) and its derivative caffeic acid phenethyl ester (CAPE) towards two triple-negative breast cancer (TNBC) cell lines, MDA-MB-231 and Hs578T, by implementation of the MTT and lactate dehydrogenase (LDH) assays. The morphological changes of breast carcinoma cells were observed following exposure to EEP and CAPE. The IC(50) of EEP was 48.35 µg∙mL(−1) for MDA-MB-23 cells and 33.68 µg∙mL(−1) for Hs578T cells, whereas the CAPE IC(50) was 14.08 µM and 8.01 µM for the MDA-MB-231 and Hs578T cell line, respectively. Here, we report that propolis and CAPE inhibited the growth of the MDA-MB-231 and Hs578T lines in a dose-dependent and exposure time-dependent manner. EEP showed less cytotoxic activity against both types of TNBC cells. EEP and, particularly, CAPE may markedly affect the viability of breast cancer cells, suggesting the potential role of bioactive compounds in chemoprevention/chemotherapy by potentiating the action of standard anti-cancer drugs. MDPI 2015-05-20 /pmc/articles/PMC6272161/ /pubmed/26007182 http://dx.doi.org/10.3390/molecules20059242 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rzepecka-Stojko, Anna
Kabała-Dzik, Agata
Moździerz, Aleksandra
Kubina, Robert
Wojtyczka, Robert D.
Stojko, Rafał
Dziedzic, Arkadiusz
Jastrzębska-Stojko, Żaneta
Jurzak, Magdalena
Buszman, Ewa
Stojko, Jerzy
Caffeic Acid Phenethyl Ester and Ethanol Extract of Propolis Induce the Complementary Cytotoxic Effect on Triple-Negative Breast Cancer Cell Lines
title Caffeic Acid Phenethyl Ester and Ethanol Extract of Propolis Induce the Complementary Cytotoxic Effect on Triple-Negative Breast Cancer Cell Lines
title_full Caffeic Acid Phenethyl Ester and Ethanol Extract of Propolis Induce the Complementary Cytotoxic Effect on Triple-Negative Breast Cancer Cell Lines
title_fullStr Caffeic Acid Phenethyl Ester and Ethanol Extract of Propolis Induce the Complementary Cytotoxic Effect on Triple-Negative Breast Cancer Cell Lines
title_full_unstemmed Caffeic Acid Phenethyl Ester and Ethanol Extract of Propolis Induce the Complementary Cytotoxic Effect on Triple-Negative Breast Cancer Cell Lines
title_short Caffeic Acid Phenethyl Ester and Ethanol Extract of Propolis Induce the Complementary Cytotoxic Effect on Triple-Negative Breast Cancer Cell Lines
title_sort caffeic acid phenethyl ester and ethanol extract of propolis induce the complementary cytotoxic effect on triple-negative breast cancer cell lines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272161/
https://www.ncbi.nlm.nih.gov/pubmed/26007182
http://dx.doi.org/10.3390/molecules20059242
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