Gu Jian-Wei, Makey Kristina L, Tucker Kevan B, Chinchar Edmund, Mao Xiaowen, Pei Ivy, Thomas Emily Y, Miele Lucio
Cancer Institute, University of Mississippi Medical Center, Jackson, Mississippi 39216, USA.
Vasc Cell. 2013 May 2;5(1):9. doi: 10.1186/2045-824X-5-9.
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.
表没食子儿茶素没食子酸酯(EGCG)作为绿茶中的主要儿茶素,其在乳腺癌治疗中的作用尚未得到充分了解。本研究检验了以下假设:EGCG可抑制缺氧诱导因子-1α(HIF-1α)和核因子κB(NFκB)的激活以及血管内皮生长因子(VEGF)的表达,从而抑制肿瘤血管生成和乳腺癌进展。将16只8周龄雌性小鼠(C57BL/6 J)左侧第四乳腺脂肪垫接种10^6个E0771(小鼠乳腺癌)细胞。8只小鼠饮用含50 - 100 mg/kg/d EGCG的水,持续4周。8只对照小鼠仅饮用普通水。使用游标卡尺监测肿瘤大小。实验结束时,采集血样、肿瘤、心脏和肢体肌肉,采用酶联免疫吸附测定(ELISA)法检测VEGF表达,采用CD31免疫组织化学法检测微血管密度(CD)。与对照组相比,EGCG治疗显著降低了肿瘤重量(0.37±0.15 vs. 1.16±0.30 g;P < 0.01)、肿瘤CD(109±20 vs. 156±12个毛细血管/mm^2;P < 0.01)、肿瘤VEGF表达(45.72±1.4 vs. 59.03±3.8 pg/mg;P < 0.01)。但是,EGCG对小鼠体重、心脏重量、心脏和骨骼肌中的血管生成及VEGF表达没有影响。与对照组相比,50μg/ml的EGCG可显著抑制培养的E0771细胞中HIF-1α和NFκB的激活以及VEGF的表达。这些研究结果支持了以下假设:EGCG作为绿茶中的主要儿茶素,直接作用于肿瘤细胞和肿瘤血管系统,从而抑制乳腺癌的肿瘤生长、增殖、迁移和血管生成,这一过程是通过抑制HIF-1α和NFκB的激活以及VEGF的表达来介导的。