首页> 美国卫生研究院文献>Journal of Angiogenesis Research >EGCG a major green tea catechin suppresses breast tumor angiogenesis and growth via inhibiting the activation of HIF-1α and NFκB and VEGF expression
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EGCG a major green tea catechin suppresses breast tumor angiogenesis and growth via inhibiting the activation of HIF-1α and NFκB and VEGF expression

机译:EGCG是一种主要的绿茶儿茶素它通过抑制HIF-1α和NFκB的激活以及VEGF的表达来抑制乳腺肿瘤的血管生成和生长。

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摘要

The role of EGCG, a major green tea catechin in breast cancer therapy is poorly understood. The present study tests the hypothesis that EGCG can inhibit the activation of HIF-1α and NFκB, and VEGF expression, thereby suppressing tumor angiogenesis and breast cancer progression. Sixteen eight-wk-old female mice (C57BL/6 J) were inoculated with 10^6 E0771 (mouse breast cancer) cells in the left fourth mammary gland fat pad. Eight mice received EGCG at 50–100 mg/kg/d in drinking water for 4 weeks. 8 control mice received drinking water only. Tumor size was monitored using dial calipers. At the end of the experiment, blood samples, tumors, heart and limb muscles were collected for measuring VEGF expression using ELISA and capillary density (CD) using CD31 immunohistochemistry. EGCG treatment significantly reduced tumor weight over the control (0.37 ± 0.15 vs. 1.16 ± 0.30 g; P < 0.01), tumor CD (109 ± 20 vs. 156 ± 12 capillary #/mm^2; P < 0.01), tumor VEGF expression (45.72 ± 1.4 vs. 59.03 ± 3.8 pg/mg; P < 0.01), respectively. But, it has no effects on the body weight, heart weight, angiogenesis and VEGF expression in the heart and skeletal muscle of mice. EGCG at 50 μg/ml significantly inhibited the activation of HIF-1α and NFκB as well as VEGF expression in cultured E0771 cells, compared to the control, respectively. These findings support the hypothesis that EGCG, a major green tea catechin, directly targets both tumor cells and tumor vasculature, thereby inhibiting tumor growth, proliferation, migration, and angiogenesis of breast cancer, which is mediated by the inhibition of HIF-1α and NFκB activation as well as VEGF expression.
机译:人们对EGCG(一种主要的绿茶儿茶素)在乳腺癌治疗中的作用了解甚少。本研究检验了以下假设:EGCG可以抑制HIF-1α和NFκB的激活以及VEGF的表达,从而抑制肿瘤血管生成和乳腺癌的进展。在左第四乳腺脂肪垫中,向16只八周大的雌性小鼠(C57BL / 6 J)接种10 ^ 6 E0771(小鼠乳腺癌)细胞。八只小鼠在饮用水中以50-100 mg / kg / d的剂量服用EGCG,持续4周。 8只对照小鼠仅接受饮用水。使用卡尺监测肿瘤大小。在实验结束时,收集血液样本,肿瘤,心脏和四肢肌肉以使用ELISA来测量VEGF表达,并使用CD31免疫组织化学来测量毛细血管密度(CD)。 EGCG治疗显着减轻了肿瘤重量(0.37±±0.15 vs. 1.16±±0.30μg; P <0.01),肿瘤CD(109±±20 vs. 156±12毛细管#/ mm ^ 2; P <0.01),肿瘤VEGF表达(分别为45.72±1.4和59.03±3.8μpg/ mg; P <0.01)。但是,它对小鼠的心脏和骨骼肌的体重,心脏重量,血管生成和VEGF表达没有影响。与对照组相比,浓度为50μg/ ml的EGCG分别显着抑制了培养的E0771细胞中HIF-1α和NFκB的活化以及VEGF的表达。这些发现支持以下假设:主要的绿茶儿茶素EGCG直接靶向肿瘤细胞和肿瘤脉管系统,从而抑制了乳腺癌的生长,增殖,迁移和血管生成,这是由抑制HIF-1α和NFκB介导的激活以及VEGF表达。

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