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从苦参中分离出的一种新型黄酮类化合物在体外表现出抗血管生成活性,降低了血管内皮生长因子(VEGF)的表达并导致G0/G1期细胞周期阻滞。

A novel flavonoid isolated from Sophora flavescens exhibited anti-angiogenesis activity, decreased VEGF expression and caused G0/G1 cell cycle arrest in vitro.

作者信息

Zhang Xiu-Li, Cao Mei-Ai, Pu Li-Ping, Huang Shuang-Sheng, Gao Qing-Xiang, Yuan Cheng-Shan, Wang Chun-Ming

机构信息

School of Life Sciences, Lanzhou University, Lanzhou, China.

出版信息

Pharmazie. 2013 May;68(5):369-75.

PMID:23802436
Abstract

Kushen, the dried root of Sophora flavescens Ait, is a traditional Chinese herbal medicine. Kushen alkaloids have been developed in China as anticancer drugs, and more potent antitumor activities have been identified in kushen flavonoids than in kushen alkaloids. In this study, the anti-angiogenic properties of (2S)-7,2',4'-triihydroxy-5-methoxy-8-dimethylallyl flavanone (Compound 1, a novel flavonoid isolated from Kushen), were examined using the human umbilical vein endothelial cell line (ECV304) in vitro. The results indicated that compound 1 shows anti-angiogenesis activity via inhibitory effects on cell proliferation, cell migration, cell adhesion, and tube formation. Further studies indicated that compound 1 blocks cell cycles in the G0/G1 phase without inducing apoptosis, and down regulates vascular endothelial growth factor (VEGF) expression. The free radical scavenging activity of compound 1 was found through 2',7'-dichlorofluorescin diacetate (DCFH-DA) incubation assay in cells. The anti-angiogenic properties of compound 1 and its antiproliferative effect on endothelial cells without causing apoptosis make it a good candidate for development as a agent against development of tumors.

摘要

苦参为豆科植物苦参的干燥根,是一种传统的中药材。苦参生物碱在中国已被开发为抗癌药物,并且已发现苦参黄酮类化合物比苦参生物碱具有更强的抗肿瘤活性。在本研究中,使用人脐静脉内皮细胞系(ECV304)在体外检测了(2S)-7,2',4'-三羟基-5-甲氧基-8-二甲基烯丙基黄烷酮(化合物1,一种从苦参中分离出的新型黄酮类化合物)的抗血管生成特性。结果表明,化合物1通过抑制细胞增殖、细胞迁移、细胞黏附和管腔形成显示出抗血管生成活性。进一步研究表明,化合物1阻滞细胞周期于G0/G1期而不诱导细胞凋亡,并下调血管内皮生长因子(VEGF)的表达。通过用二氯荧光素二乙酸酯(DCFH-DA)孵育细胞检测发现了化合物1的自由基清除活性。化合物1的抗血管生成特性及其对内皮细胞的抗增殖作用而不引起细胞凋亡,使其成为开发抗肿瘤药物的良好候选物。

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