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首页> 外文期刊>Cancer biotherapy and radiopharmaceuticals >Low-dose docetaxel combined with (-)-epigallocatechin-3-gallate inhibits angiogenesis and tumor growth in nude mice with gastric cancer xenografts
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Low-dose docetaxel combined with (-)-epigallocatechin-3-gallate inhibits angiogenesis and tumor growth in nude mice with gastric cancer xenografts

机译:低剂量多西他赛联合(-)-表没食子儿茶素-3-没食子酸酯可抑制胃癌异种移植裸鼠的血管生成和肿瘤生长

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摘要

Low-dose metronomic (LDM) chemotherapy represents a new strategy to treat solid tumors by stronger antiangiogenic activity and less side-effects, especially in combination with other antiangiogenic agents. The aim of the study is to investigate the antiangiogenic effect of docetaxel alone and combined with (-)-epigallocatechin-3-gallate (EGCG) in preclinical settings of gastric cancer. BGC-823 human gastric cancer xenograft model was used, and tumor growth, side-effects of mice were closely monitored. Expression of vascular endothelial growth factor and CD31 were observed by immunohistochemistry, and microvessel density of the tumor tissues was assessed by CD31 immunohistochemical analysis. Our results indicated that LDM docetaxel inhibited angiogenesis and growth of gastric cancer with less toxicity, and the effects were further enhanced by the concurrent administration of EGCG. Our study, for the first time, rationally demonstrated that LDM docetaxel treatment used alone or combined with EGCG is effective and safe in preclinical settings of gastric cancer. Our data suggest that LDM docetaxel used alone or combined with EGCG may be an innovative and promising therapeutic strategy in the experimental treatment of human gastric cancer.
机译:低剂量节律(LDM)化疗代表了一种通过增强抗血管生成活性和减少副作用(特别是与其他抗血管生成剂联合使用)来治疗实体瘤的新策略。该研究的目的是研究多西他赛单独和联合(-)-表没食子儿茶素-3-没食子酸酯(EGCG)在胃癌的临床前环境中的抗血管生成作用。使用BGC-823人胃癌异种移植模型,并密切监测小鼠的肿瘤生长,副作用。通过免疫组织化学观察血管内皮生长因子和CD31的表达,并通过CD31免疫组织化学分析评估肿瘤组织的微血管密度。我们的结果表明,LDM多西紫杉醇可抑制胃癌的血管生成和生长,且毒性较小,并且同时给予EGCG可进一步增强其作用。我们的研究首次合理地证明,单独使用LDM多西紫杉醇或与EGCG联合使用在胃癌的临床前治疗中是安全有效的。我们的数据表明,单独或与EGCG一起使用的LDM多西紫杉醇可能是人胃癌实验治疗中的一种创新且有希望的治疗策略。

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