首页> 外文期刊>Polish journal of veterinary sciences >Synergistic interactions between resveratrol and doxorubicin inhibit angiogenesis both in vitro and in vivo
【24h】

Synergistic interactions between resveratrol and doxorubicin inhibit angiogenesis both in vitro and in vivo

机译:白藜芦醇和多柔比蛋白之间的协同相互作用在体外和体内抑制血管生成

获取原文
获取原文并翻译 | 示例
       

摘要

Resveratrol is a polyphenolic compound which is found in many nutrients including grapes, peanuts, raspberries, and apples. Anti-proliferative, anti-angiogenic and apoptotic effects of resveratrol have been shown on various cancer cells. Doxorubicin is considered as one of the most effective anticancer agents and reveals its antitumor activity by induction of apoptosis and inhibition of angiogenesis. Our study reports for the first time the potent ability of resveratrol in combination with doxorubicin to inhibit angiogenesis in vitro and in vivo. The cytotoxic effect of resveratrol (1.56-100 mu M), doxorubicin (0.01-0.92 mu M) and their combination were analyzed in the human umbilical vein endothelial cells (HUVECs) by ATP assay. In vitro angiogenesis was evaluated using tube formation assay in HUVECs. In vivo anti-angiogenic activity was assessed in a chick chorioallantoic membrane (CAM) model using fertilized chicken eggs. All test groups were compared to thalidomide as a positive control, three concentrations of resveratrol (10-5-2.5 mu g/pellet) and a 2 mu g/pellet concentration of doxorubicin was examined. All data were evaluated statistically. Resveratrol and doxorubicin alone displayed inhibitory effects on angiogenesis and cell viability at higher doses. However, the combination of resveratrol and doxorubicin exhibited a significant dose-dependent inhibition of CAM angiogenesis in vivo as well as proliferation and tube formation in HUVECs compared to the positive control (+/-)-thalidomide. Our results suggest that resveratrol in combination with doxorubicin is a novel strategy in the prevention and treatment of angiogenesis
机译:白藜芦醇是一种多酚化合物,存在于葡萄、花生、覆盆子和苹果等多种营养物质中。白藜芦醇对多种癌细胞具有抗增殖、抗血管生成和凋亡作用。阿霉素被认为是最有效的抗癌药物之一,通过诱导细胞凋亡和抑制血管生成显示其抗肿瘤活性。我们的研究首次报道了白藜芦醇与阿霉素联合在体外和体内抑制血管生成的有效能力。采用ATP法分析白藜芦醇(1.56-100μM)、阿霉素(0.01-0.92μM)及其组合对人脐静脉内皮细胞(HUVECs)的细胞毒性作用。体外血管生成通过HUVEC中的试管形成试验进行评估。利用受精鸡蛋在鸡绒毛尿囊膜(CAM)模型中评估了体内抗血管生成活性。将所有试验组与沙利度胺作为阳性对照进行比较,检查三种浓度的白藜芦醇(10-5-2.5μg/粒)和2μg/粒浓度的阿霉素。对所有数据进行统计评估。在较高剂量下,白藜芦醇和阿霉素单独对血管生成和细胞活力有抑制作用。然而,与阳性对照(+/-)-沙利度胺相比,白藜芦醇和阿霉素联合应用对体内CAM血管生成以及HUVECs的增殖和管形成表现出显著的剂量依赖性抑制。我们的结果表明,白藜芦醇联合阿霉素是一种预防和治疗血管生成的新策略

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号