Flavonoids from persimmon (Diospyros kaki L.) leaves inhibit proliferation and induce apoptosis in PC-3 cells by activation of oxidative stress and mitochondrial apoptosis

被引:33
作者
Ding, Yan [1 ]
Ren, Kai [2 ,3 ]
Dong, Huanhuan [1 ]
Song, Fei [1 ]
Chen, Jing [1 ]
Guo, Youtian [1 ]
Liu, Yanshan [1 ]
Tao, Weijie [1 ]
Zhang, Yali [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Minist Educ, Key Lab Biomed Informat Engn, Xian 710049, Shaanxi, Peoples R China
[2] Xian Med Univ, Dept Biochem & Mol Biol, Xian 710021, Shaanxi, Peoples R China
[3] Univ Torino, Mol Biotechnol Ctr, Dept Mol Biotechnol, Turin, Italy
基金
中国国家自然科学基金;
关键词
Persimmon leaves; Flavonoids; Cytotoxicity; Oxidative stress; Apoptosis; Prostate cancer; CANCER PREVENTION; ANTIOXIDANT; QUERCETIN; MECHANISMS; JAPANESE; EXTRACT;
D O I
10.1016/j.cbi.2017.07.026
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
Persimmon (Diospyros kaki L.) leaves are extensively used in Chinese medicine and are also excellent source of dietary polyphenols. Here we investigated the antiproliferative and pro-apoptotic activity of the total flavonoids extracted from persimmon leaves (FPL) in PC-3 cells. After treating cells with different concentration of FPL, Quercetin or Rutin for 24 h, MTT and flow cytometry were used to measure the cytotoxicity, apoptotic rate and cell cycle arrest. Compared with Quercetin and Rutin, FPL showed higher cytotoxicity at 12.5 and 25 mu g/ml concentrations and also presented lower IC50 in PC-3 cells. In addition, FPL induced PC-3 cells apoptosis by activation of oxidative stress, as detected by ROS, MDA, nitrite and iNOS activity, and increased mitochondrial membrane permeability. Morphological changes, inactivation of Bcl-2, upregulation of BAX, release of cytochrome c and activation of downstream apoptotic signaling in FPL-treated PC-3 cells also suggested apoptotic death. Meanwhile, FPL significantly inhibited migration of PC-3 cells. Therefore, FPL inhibited proliferation, migration and induced apoptosis of PC-3 cells by activation of oxidative stress and mitochondrial-related apoptosis. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:210 / 217
页数:8
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