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

被引:56
|
作者
Rzepecka-Stojko, Anna [1 ]
Kabala-Dzik, Agata [2 ]
Mozdzierz, Aleksandra [3 ]
Kubina, Robert [2 ]
Wojtyczka, Robert D. [4 ]
Stojko, Rafal [5 ]
Dziedzic, Arkadiusz [6 ]
Jastrzebska-Stojko, Zaneta [7 ]
Jurzak, Magdalena [8 ]
Buszman, Ewa [1 ]
Stojko, Jerzy [3 ]
机构
[1] Med Univ Silesia, Dept Pharmaceut Chem, Sch Pharm, Div Lab Med Sosnowiec, PL-41200 Sosnowiec, Poland
[2] Med Univ Silesia, Dept Pathol, Sch Pharm, Div Lab Med Sosnowiec, PL-41200 Sosnowiec, Poland
[3] Med Univ Silesia, Dept Hyg Bioanal & Environm Studies, Sch Pharm, Div Lab Med Sosnowiec, PL-41200 Sosnowiec, Poland
[4] Med Univ Silesia, Dept & Inst Microbiol & Virol, Sch Pharm, Div Lab Med Sosnowiec, PL-41200 Sosnowiec, Poland
[5] Med Univ Silesia, Dept Women Hlth, Sch Hlth Sci, PL-40752 Katowice, Poland
[6] Med Univ Silesia, Div Dent Zabrze, Sch Med, Dept Conservat Dent Endodont, PL-41902 Bytom, Poland
[7] Med Univ Silesia, Sch Med, Dept Anesthesiol & Intens Care, PL-40752 Katowice, Poland
[8] Med Univ Silesia, Dept Cosmetol, Sch Pharm, Div Lab Med Sosnowiec, PL-41200 Sosnowiec, Poland
来源
MOLECULES | 2015年 / 20卷 / 05期
关键词
caffeic acid phenethyl ester; propolis; cytotoxicity; breast cancer; NF-KAPPA-B; IN-VITRO; SYNTHETIC DERIVATIVES; GREEN PROPOLIS; COLON-CANCER; APOPTOSIS; CAPE; ANTIOXIDANT; GROWTH; COMBINATION;
D O I
10.3390/molecules20059242
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 IC50 of EEP was 48.35 mu g.mL(-1) for MDA-MB-23 cells and 33.68 mu g.mL(-1) for Hs578T cells, whereas the CAPE IC50 was 14.08 mu M and 8.01 mu M 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.
引用
收藏
页码:9242 / 9262
页数:21
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