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Journal of Zhejiang University-SCIENCE B (Biomedicine & Biotechnology)  2017, Vol. 18 Issue (2): 89-98    DOI: 10.1631/jzus.B1600022
Articles     
Green tea polyphenols induce cell death in breast cancer MCF-7 cells through induction of cell cycle arrest and mitochondrial-mediated apoptosis
Shu-min Liu, Shi-yi Ou, Hui-hua Huang
Department of Food Science and Engineering, South China University of Technology, Guangzhou 510641, China; Department of Food Science and Engineering, Jinan University, Guangzhou 510632, China
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Abstract  In order to study the molecular mechanisms of green tea polyphenols (GTPs) in treatment or prevention of breast cancer, the cytotoxic effects of GTPs on five human cell lines (MCF-7, A549, Hela, PC3, and HepG2 cells) were determined and the antitumor mechanisms of GTPs in MCF-7 cells were analyzed. The results showed that GTPs exhibited a broad spectrum of inhibition against the detected cancer cell lines, particularly the MCF-7 cells. Studies on the mechanisms revealed that the main modes of cell death induced by GTPs were cell cycle arrest and mitochondrial-mediated apoptosis. Flow cytometric analysis showed that GTPs mediated cell cycle arrest at both G1/M and G2/M transitions. GTP dose dependently led to apoptosis of MCF-7 cells via the mitochondrial pathways, as evidenced by induction of chromatin condensation, reduction of mitochondrial membrane potential (ΔΨm), improvement in the generation of reactive oxygen species (ROS), induction of DNA fragmentation, and activations of caspase-3 and caspase-9 in the present paper.

Key wordsGreen tea polyphenol (GTP)      Breast cancer      MCF-7 cells      Mitochondrial-mediated apoptosis      Cell death      Cell cycle arrest     
Received: 26 January 2016      Published: 26 January 2017
CLC:  R737.9  
Cite this article:

Shu-min Liu, Shi-yi Ou, Hui-hua Huang. Green tea polyphenols induce cell death in breast cancer MCF-7 cells through induction of cell cycle arrest and mitochondrial-mediated apoptosis. Journal of Zhejiang University-SCIENCE B (Biomedicine & Biotechnology), 2017, 18(2): 89-98.

URL:

http://www.zjujournals.com/xueshu/zjus-b/10.1631/jzus.B1600022     OR     http://www.zjujournals.com/xueshu/zjus-b/Y2017/V18/I2/89

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