Hsu Y L, Kuo P L, Tzeng W S, Lin C C
Graduate Institute of Natural Products, College of Pharmacy, Kaohsiung Medical University, 100 Shih-Chuan 1st Road, Kaohsiung 807, Taiwan.
Food Chem Toxicol. 2006 May;44(5):704-13. doi: 10.1016/j.fct.2005.10.003. Epub 2005 Nov 22.
Chalcones are discussed to represent cancer preventive food components in a human diet that is rich in fruits and vegetables. In this study, we examined chalcone (1,3-diphenyl-2-propenone) for its effect on proliferation in human breast cancer cell lines, MCF-7 and MDA-MB-231. The results showed that chalcone inhibited the proliferation of MCF-7 and MDA-MB-231 by inducing apoptosis and blocking cell cycle progression in the G2/M phase. Immunoblot assay showed that chalcone significantly decreased the expression of cyclin B1, cyclin A and Cdc2 protein, as well as increased the expression of p21 and p27 in a p53-independent manner, contributing to cell cycle arrest. An enhancement in Fas/APO-1 and its two form ligands, membrane-bound Fas ligand (mFasL) and soluble Fas ligand (sFasL), was responsible for the apoptotic effect induced by chalcone. In addition, chalcone also triggered the mitochondrial apoptotic signaling by increasing the amount of Bax and Bak and reducing the level of Bcl-2 and Bcl-X(L), and subsequently activated caspase-9 in MCF-7 and MDA-MB-231 cells. Taken together, our study suggests that the blockade of cell cycle progression and initiation of cell apoptotic system may participate in the antiproliferative activity of chalcone in human breast cancer cells.
查耳酮被认为是人类富含水果和蔬菜饮食中的癌症预防食物成分。在本研究中,我们检测了查耳酮(1,3 - 二苯基 - 2 - 丙烯酮)对人乳腺癌细胞系MCF - 7和MDA - MB - 231增殖的影响。结果表明,查耳酮通过诱导凋亡和阻断细胞周期在G2/M期的进程来抑制MCF - 7和MDA - MB - 231的增殖。免疫印迹分析表明,查耳酮以不依赖p53的方式显著降低细胞周期蛋白B1、细胞周期蛋白A和Cdc2蛋白的表达,同时增加p21和p27的表达,从而导致细胞周期停滞。Fas/APO - 1及其两种形式的配体,即膜结合型Fas配体(mFasL)和可溶性Fas配体(sFasL)的增强,是查耳酮诱导凋亡效应的原因。此外,查耳酮还通过增加Bax和Bak的量以及降低Bcl - 2和Bcl - X(L)的水平触发线粒体凋亡信号,并随后在MCF - 7和MDA - MB - 231细胞中激活caspase - 9。综上所述,我们的研究表明,细胞周期进程的阻断和细胞凋亡系统的启动可能参与了查耳酮对人乳腺癌细胞的抗增殖活性。