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桑椹花青素、矢车菊素 3-芸香糖苷和矢车菊素 3-葡萄糖苷对人肺癌细胞系的迁移和侵袭具有抑制作用。

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.

作者信息

Chen Pei-Ni, Chu Shu-Chen, Chiou Hui-Ling, Kuo Wu-Hsien, Chiang Chui-Liang, Hsieh Yih-Shou

机构信息

Institute of Biochemistry, Chung Shan Medical University, No 110, Section 1, Chien Kuo N. Road, Taichung 402, Taiwan, ROC.

出版信息

Cancer Lett. 2006 Apr 28;235(2):248-59. doi: 10.1016/j.canlet.2005.04.033. Epub 2005 Jun 22.

DOI:10.1016/j.canlet.2005.04.033
PMID:15975709
Abstract

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-kappaB. 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.

摘要

花青素作为天然色素存在于各种水果和蔬菜中,其具有多种生物活性特性已得到充分表征,并因其抗氧化特性而被广泛使用。此外,最近的研究揭示了花青素具有多效抗癌和抗增殖能力。浆果提取物含有大量花青素,常用于饮食或某些治疗应用中。在本研究中,我们首先观察到矢车菊素3-芸香糖苷和矢车菊素3-葡萄糖苷(从桑白皮中提取)对高转移性A549人肺癌细胞的迁移和侵袭具有剂量依赖性抑制作用,且无细胞毒性。结果表明,矢车菊素3-葡萄糖苷和矢车菊素3-芸香糖苷处理可剂量依赖性地降低基质金属蛋白酶-2(MMP-2)和尿激酶型纤溶酶原激活剂(u-PA)的表达,并增强基质金属蛋白酶组织抑制剂-2(TIMP-2)和纤溶酶原激活剂抑制剂(PAI)的表达。半定量RT-PCR进一步分析表明,这些改变均发生在转录水平。此外,矢车菊素3-芸香糖苷和矢车菊素3-葡萄糖苷处理还导致c-Jun和NF-κB的激活受到抑制。综上所述,这些结果表明花青素可降低癌细胞的体外侵袭性,因此在开发潜在的癌症治疗方法中可能具有重要价值。

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