Mulberry anthocyanins, cyanidin 3-rutinoside and cyanidin 3-glucoside, exhibited an inhibitory effect on the migration and invasion of a human lung cancer cell line

被引:315
作者
Chen, Pei-Ni
Chu, Shu-Chen
Chiou, Hui-Ling
Kuo, Wu-Hsien
Chiang, Chui-Liang
Hsieh, Yih-Shou
机构
[1] Chung Shan Med Univ, Inst Biochem, Taichung 402, Taiwan
[2] Chungtai Inst Hlth Sci & Technol, Dept Food Sci, Taichung 406, Taiwan
[3] Chung Shan Med Univ, Sch Med Technol, Taichung 402, Taiwan
关键词
anthocyanins; migration; invasion; MMP-2; u-PA; inhibitory effect; mulberry;
D O I
10.1016/j.canlet.2005.04.033
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Anthocyanins, present in various fruits and vegetables as natural colorant, have been well characterized to be involved in various bioactive properties and are wildly used for their antioxidant properties. Furthermore, recent studies have revealed pleiotropic anticancer and antiproliferative capabilities of anthocyanin. Berry extract contains high amounts of anthocyanins and is commonly used in diet or in some therapeutic applications. In this study, we first observed that cyanidin 3-rutinoside and cyanidin 3-glucoside (extracted from Morus alba L.) exerted a dose-dependent inhibitory effect on the migration and invasion, of highly metastatic A549 human lung carcinoma cells in absence of cytotoxicity. The results showed that cyanidin 3-glucoside and cyanidin 3-rutinoside treatments could decrease the expressions of matrix matalloprotinase-2 (MMP-2) and urokinase-plasminogen activator (u-PA) in a dose-dependent manner and enhance the expression of tissue inhibitor of matrix matalloprotinase-2 (TIMP-2) and plasminogen activator inhibitor (PAI). Further analysis with semi-quantitative RT-PCR showed that these alterations were all on the transcriptional level. Further, a treatment of cyanidin 3-rutinoside and cyanidin 3-glucoside also resulted in an inhibition on the activation of c-Jun and NF-kappa B. Together, these result suggested that anthocyanins could decrease the in vitro invasiveness of cancer cells and therefore, may be of great value in developing a potential cancer therapy. (c) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:248 / 259
页数:12
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