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Wogonin suppresses tumor growth in vivo and VEGF-induced angiogenesis through inhibiting tyrosine phosphorylation of VEGFR2

机译:Wogonin通过抑制VEGFR2的酪氨酸磷酸化来抑制体内肿瘤生长和VEGF诱导的血管生成

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摘要

Previous studies revealed that wogonin, a naturally occurring monoflavonoid extracted from Scutellariae radix, possessed anticancer activity both in vitro and in vivo. However, the molecular mechanism of its potent anticancer activity remains poorly understood and warrants further investigations. In this study, we found for the first time that wogonin inhibited the growth and tumor angiogenesis of human gastric carcinoma in nude mice. We explored the inhibitory effect of wogonin on angiogenesis stimulated by vascular endothelial growth factor (VEGF) in vitro. Wogonin suppressed the VEGF-stimulated migration and tube formation of human umbilical vein endothelial cells (HUVECs). It also restrained VEGF-induced tyrosine phosphorylation of vascular endothelial growth factor receptor 2 (VEGFR2). This inhibition of receptor phosphorylation was correlated with a significant decrease in VEGF-triggered phosphorylated forms of ERK, AKT and p38. Taken together, these findings strongly suggest that wogonin might be a promising antitumor drug. (c) 2008 Elsevier Inc. All rights reserved.
机译:先前的研究表明,wogonin是从黄cut中提取的一种天然存在的类黄酮,在体外和体内均具有抗癌活性。然而,其有效的抗癌活性的分子机制仍知之甚少,值得进一步研究。在这项研究中,我们首次发现wogonin抑制裸鼠人胃癌的生长和肿瘤血管生成。我们探讨了wogonin对体外血管内皮生长因子(VEGF)刺激血管生成的抑制作用。 Wogonin抑制了VEGF刺激的人脐静脉内皮细胞(HUVEC)迁移和管形成。它也抑制了VEGF诱导的血管内皮生长因子受体2(VEGFR2)酪氨酸磷酸化。受体磷酸化的这种抑制与VEGF触发的ERK,AKT和p38磷酸化形式的显着减少有关。综上所述,这些发现强烈表明沃戈宁可能是一种有前途的抗肿瘤药物。 (c)2008 Elsevier Inc.保留所有权利。

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