25-Methoxyhispidol A, a novel triterpenoid of Poncirus trifoliata, inhibits cell growth via the modulation of EGFR/c-Src signaling pathway in MDA-MB-231 human breast cancer cells

被引:19
作者
Chung, Hwa-Jin
Park, Eun-Jung [2 ]
Pyee, Yuna
Xu, Guang Hua [3 ]
Lee, Seung-Ho [3 ]
Kim, Young Shik
Lee, Sang Kook [1 ]
机构
[1] Seoul Natl Univ, Inst Nat Prod Res, Coll Pharm, Seoul 151742, South Korea
[2] Ewha Womans Univ, Coll Pharm, Seoul 120750, South Korea
[3] Yeungnam Univ, Coll Pharm, Kyongsan 712749, South Korea
关键词
25-Methoxyhispidol A; Poncirus trifoliata; MDA-MB-231; Cell cycle arrest; c-Src; EGFR; FACTOR RECEPTOR;
D O I
10.1016/j.fct.2011.07.001
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
The fruit of Poncirus tnfoliata (Rutaceae) has been used a medicinal food and traditional medicine. Recently we reported the isolation of 25-methoxyhispidol A (25-MHA) as a novel triterpenoid from the immature fruit of P. tnfoliata with the potential growth inhibition of cancer cells. However, the molecular mechanisms on the anti-proliferative activity in cancer cells remain to be elucidated. In the present study, we investigated the anti-proliferative activity and mechanisms of actions mediated by 25-MHA in estrogen receptor (ER)-negative MDA-MB-231 human breast cancer cells. 25-MHA exhibited the growth inhibitory activity against MDA-MB-231 cells with the cell cycle arrest in the G0/G1 phase. The cell cycle arrest in the G0/G1 by 25-MHA was well correlated with the downregulation of cyclin D1, cyclin dependent kinase (CDK4), CDK2, cyclin A, phosphorylated retinoblastoma protein (pRb), and induction of cdk inhibitor p21(WAF1/Cip1) protein. 25-MHA also suppressed the activation of c-Src/epidermal growth factor receptor (EGFR)/Akt signaling, and consequently led to the inactivation of mTOR and its downstream signal molecules including 4E-binding protein (4E-BP) and p70 S6 kinase. These findings suggest that 25-MHA-mediated inhibitory activity of human breast cancer cell growth might be related with the cell cycle arrest and modulation of signal transduction pathways. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2942 / 2946
页数:5
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