Apigenin Reduces Survival of Choriocarcinoma Cells by Inducing Apoptosis via the PI3K/AKT and ERK1/2 MAPK Pathways

被引:65
|
作者
Lim, Whasun [1 ]
Park, Sunwoo [1 ]
Bazer, Fuller W. [2 ]
Song, Gwonhwa [1 ]
机构
[1] Korea Univ, Dept Biotechnol, Coll Life Sci & Biotechnol, Seoul 136713, South Korea
[2] Texas A&M Univ, Dept Anim Sci, Ctr Anim Biotechnol & Genom, College Stn, TX 77843 USA
关键词
HUMAN LUNG-CANCER; GROWTH-FACTOR; DEPENDENT PATHWAYS; SIGNALING PATHWAY; PROSTATE-CANCER; CARCINOMA CELLS; TUMOR-GROWTH; ACTIVATION; INVASION; PROLIFERATION;
D O I
10.1002/jcp.25372
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Apigenin is a flavonoid found in parsley, onions, oranges, tea, chamomile, wheat, and sprouts. It has a variety of biological properties including anti-oxidant, anti-mutagenic, anti-carcinogenic, anti-inflammatory, anti-proliferative, and anti-spasmodic effects. Based on epidemiological and case-control studies, apigenin is regarded as a novel chemotherapeutic agent against various cancer types. However, little is known about the effects of apigenin on choriocarcinoma cells. Therefore, we investigated the anti-cancer effects of apigenin on choriocarcinoma cells (JAR and JEG3) in the present study. Apigenin reduced viability and migratory properties, increased apoptosis, and suppressed mitochondrial membrane potential in both the JAR and JEG3 cells. In addition, apigenin predominantly decreased phosphorylation of AKT, P70RSK, and S6 whereas the phosphorylation of ERK1/2 and P90RSK was increased by apigenin treatment of JAR and JEG3 cells in a dose-dependent manner. Moreover, treatment of JAR and JEG3 cells with both apigenin and pharmacological inhibitors of PI3K/AKT (LY294002) and ERK1/2 (U0126) revealed synergistic anti-proliferative effects. Collectively, these results indicated that the apigenin is an invaluable chemopreventive agent that inhibits progression and metastasis of choriocarcinoma cells through regulation of PI3K/AKT and ERK1/2 MAPK signal transduction mechanism. (C) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:2690 / 2699
页数:10
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