Pro-oxidant and pro-apoptotic activity of polyphenol extract from Annurca apple and its underlying mechanisms in human breast cancer cells

被引:81
作者
D'Angelo, Stefania [1 ,2 ]
Martino, Elisa [2 ]
Ilisso, Concetta Paola [2 ]
Bagarolo, Maria Libera [2 ]
Porcelli, Marina [2 ]
Cacciapuoti, Giovanna [2 ]
机构
[1] Parthenope Univ, Dept Motor Sci & Wellness, Naples, Italy
[2] Univ Campania Luigi Vanvitelli, Dept Biochem Biophys & Gen Pathol, Via L De Crecchio 7, I-80138 Naples, Italy
关键词
Annurca apple; polyphenol extract; lipid peroxidation; pro-oxidant; breast cancer; apoptosis; cell cycle; ERK1/2; signaling; REACTIVE OXYGEN; NATURAL-PRODUCTS; REDOX REGULATION; GROWTH; ANTICANCER; DEATH; DEGRADATION; ANTIOXIDANT; INHIBITION; ACTIVATION;
D O I
10.3892/ijo.2017.4088
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Among nutraceuticals, polyphenols represent the most intriguing and studied class of compounds that can be therapeutics for a large spectrum of the most common diseases, including cancer. Although polyphenols are well known as potent antioxidants, a pro-oxidant effect has been associated with a pro-apoptotic function of these compounds in various types of tumor cells. Annurca apple, a southern Italian variety, is characterized by an extremely high content of polyphenols and displays a stronger antioxidant activity compared with other varieties. In the present study we explored the antiproliferative effect of Annurca apple poly phenol extract (APE) in human breast cancer MCF-7 cells and we investigated the underlying mechanisms. Results showed that at 500 mu M catechin equivalent (EqC) APE acts as a pro-oxidant increasing thiobarbituric acid-reactive species cell content of approximately 6-fold more than the untreated cells. We found that APE strongly inhibits the proliferation of MCF-7 cells by inducing G2/M cell cycle arrest and apoptosis. Immunoblot analysis demonstrated that APE treatment increases the levels of p53 and p21, downregulates the expression of the cell cycle regulatory protein cyclin D1, and inhibits ERK1/2 phosphorylation. Moreover, APE treatment caused a marked increase of pro-apoptotic Bax/Bcl-2 ratio paralleled by caspase-9,-6,-7, and poly(ADP ribose) polymerase cleavage. Altogether our data indicate that APE, at elevated concentrations, acts as a potent pro-oxidant and antiproliferative agent able to downregulate ERK1/2 pathway leading to cell cycle inhibition and apoptosis and provides a rationale for its potential use in the development of novel therapeutics towards breast cancer.
引用
收藏
页码:939 / 948
页数:10
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