Hydroxytyrosol Protects against Oxidative DNA Damage in Human Breast Cells

被引:115
作者
Warleta, Fernando [1 ]
Sanchez Quesada, Cristina [1 ]
Campos, Maria [1 ]
Allouche, Yosra [1 ,2 ]
Beltran, Gabriel [2 ]
Gaforio, Jose J. [1 ]
机构
[1] Univ Jaen, Div Immunol, Dept Hlth Sci, Fac Expt Sci, Jaen 23071, Spain
[2] Ctr Venta Llano, Pesquera Prod Ecol IFAPA, Inst Andaluz Invest & Formac Agr, Mengibar 23620, Spain
关键词
breast cancer; Mediterranean diet; olive oil minor compounds; hydroxytyrosol; tyrosol; phenols; oxidative stress; reactive oxygen species; DNA damage; OLIVE OIL PHENOLICS; ANTIOXIDANT PROPERTIES; EPITHELIAL-CELLS; CANCER CELLS; CARCINOGENESIS; TYROSOL; STRESS; HEALTH; LINES; ASSAY;
D O I
10.3390/nu3100839
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Over recent years, several studies have related olive oil ingestion to a low incidence of several diseases, including breast cancer. Hydroxytyrosol and tyrosol are two of the major phenols present in virgin olive oils. Despite the fact that they have been linked to cancer prevention, there is no evidence that clarifies their effect in human breast tumor and non-tumor cells. In the present work, we present hydroxytyrosol and tyrosol's effects in human breast cell lines. Our results show that hydroxytyrosol acts as a more efficient free radical scavenger than tyrosol, but both fail to affect cell proliferation rates, cell cycle profile or cell apoptosis in human mammary epithelial cells (MCF10A) or breast cancer cells (MDA-MB-231 and MCF7). We found that hydroxytyrosol decreases the intracellular reactive oxygen species (ROS) level in MCF10A cells but not in MCF7 or MDA-MB-231 cells while very high amounts of tyrosol is needed to decrease the ROS level in MCF10A cells. Interestingly, hydroxytyrosol prevents oxidative DNA damage in the three breast cell lines. Therefore, our data suggest that simple phenol hydroxytyrosol could contribute to a lower incidence of breast cancer in populations that consume virgin olive oil due to its antioxidant activity and its protection against oxidative DNA damage in mammary cells.
引用
收藏
页码:839 / 857
页数:19
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