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Dose-dependent benefits of quercetin on tumorigenesis in the C3(1)/SV40Tag transgenic mouse model of breast cancer

机译:槲皮素在乳腺癌C3(1)/ SV40Tag转基因小鼠模型中对肿瘤发生的剂量依赖性益处

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Breast cancer is the leading cause of cancer related death in women. Quercetin is a flavonol shown to have anti-carcinogenic actions. However, few studies have investigated the dose-dependent effects of quercetin on tumorigenesis and none have used the C3(1)/SV40 Tag breast cancer mouse model. At 4 weeks of age female C3(1)/SV40 Tag mice were randomized to one of four dietary treatments (n = 15-16/group): control (no quercetin), low-dose quercetin (0.02% diet), moderate-dose quercetin (0.2% diet), or high-dose quercetin (2% diet). Tumor number and volume was assessed twice a week and at sacrifice (20 wks). Results showed an inverted 'U' dose-dependent effect of dietary quercetin on tumor number and volume; at sacrifice the moderate dose was most efficacious and reduced tumor number 20% and tumor volume 78% compared to control mice (C3-Con: 9.0 +/- 0.9; C3-0.2%: 7.3 +/- 0.9) and (C3-Con: 2061.8 +/- 977.0 mm(3); and C3-0.2%: 462.9 +/- 75.9 mm(3)). Tumor volume at sacrifice was also reduced by the moderate dose compared to the high and low doses (C3-2%: 1163.2 +/- 305.9 mm(3); C3-0.02%: 1401.5 +/- 555.6 mm(3)), as was tumor number (C3-2%: 10.7 +/- 1.3 mm(3); C3-0.02%: 8.1 +/- 1.1 mm(3)). Gene expression microarray analysis performed on mammary glands from C3-Con and C3-0.2% mice determined that 31 genes were down-regulated and 9 genes were up-regulated more than 2-fold (P < 0.05) by quercetin treatment. We report the novel finding that there is a distinct dose-dependent effect of quercetin on tumor number and volume in a transgenic mouse model of human breast cancer, which is associated with a specific gene expression signature related to quercetin treatment.
机译:乳腺癌是女性癌症相关死亡的主要原因。槲皮素是一种黄酮醇,具有抗癌作用。但是,很少有研究研究槲皮素对肿瘤发生的剂量依赖性作用,没有研究使用C3(1)/ SV40 Tag乳腺癌小鼠模型。在4周龄时,将雌性C3(1)/ SV40 Tag小鼠随机分配至以下四种饮食疗法之一(n = 15-16 /组):对照组(无槲皮素),低剂量槲皮素(饮食为0.02%),中度-剂量槲皮素(饮食为0.2%)或大剂量槲皮素(饮食为2%)。每周两次并且处死时(20周)评估肿瘤的数量和体积。结果表明,膳食槲皮素对肿瘤的数量和体积呈“ U”型剂量依赖性。与对照小鼠(C3-Con:9.0 +/- 0.9; C3-0.2%:7.3 +/- 0.9)和(C3-Con)相比,在处死时,中等剂量最有效并且肿瘤数目减少了20%,肿瘤体积减少了78%。 :2061.8 +/- 977.0毫米(3);和C3-0.2%:462.9 +/- 75.9毫米(3))。与高剂量和低剂量相比,处死剂量的肿瘤体积也减少了中等剂量(C3-2%:1163.2 +/- 305.9 mm(3); C3-0.02%:1401.5 +/- 555.6 mm(3)),肿瘤数目(C3-2%:10.7 +/- 1.3毫米(3); C3-0.02%:8.1 +/- 1.1毫米(3))。对槲皮素处理的C3-Con和C3-0.2%小鼠的乳腺进行的基因表达微阵列分析确定31个基因被下调,而9个基因被上调2倍以上(P <0.05)。我们报告了这一新发现,槲皮素对人类乳腺癌的转基因小鼠模型中的肿瘤数量和体积具有明显的剂量依赖性效应,这与与槲皮素治疗相关的特定基因表达特征有关。

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