Crew K D, Ho K A, Brown P, Greenlee H, Bevers T B, Arun B, Sneige N, Hudis C, McArthur H L, Chang J, Rimawi M, Cornelison T L, Cardelli J, Santella R M, Wang A, Lippman S M, Hershman D L
Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY, USA.
University of Texas, MD Anderson Cancer Center, Houston, TX, USA.
J Hum Nutr Diet. 2015 Jun;28(3):272-82. doi: 10.1111/jhn.12229. Epub 2014 Mar 19.
Observational and experimental data support a potential breast cancer chemopreventive effect of green tea.
We conducted an ancillary study using archived blood/urine from a phase IB randomised, placebo-controlled dose escalation trial of an oral green tea extract, Polyphenon E (Poly E), in breast cancer patients. Using an adaptive trial design, women with stage I-III breast cancer who completed adjuvant treatment were randomised to Poly E 400 mg (n = 16), 600 mg (n = 11) and 800 mg (n = 3) twice daily or matching placebo (n = 10) for 6 months. Blood and urine collection occurred at baseline, and at 2, 4 and 6 months. Biological endpoints included growth factor [serum hepatocyte growth factor (HGF), vascular endothelial growth factor (VEGF)], lipid (serum cholesterol, triglycerides), oxidative damage and inflammatory biomarkers.
From July 2007-August 2009, 40 women were enrolled and 34 (26 Poly E, eight placebo) were evaluable for biomarker endpoints. At 2 months, the Poly E group (all dose levels combined) compared to placebo had a significant decrease in mean serum HGF levels (-12.7% versus +6.3%, P = 0.04). This trend persisted at 4 and 6 months but was no longer statistically significant. For the Poly E group, serum VEGF decreased by 11.5% at 2 months (P = 0.02) and 13.9% at 4 months (P = 0.05) but did not differ compared to placebo. At 2 months, there was a trend toward a decrease in serum cholesterol with Poly E (P = 0.08). No significant differences were observed for other biomarkers.
Our findings suggest potential mechanistic actions of tea polyphenols in growth factor signalling, angiogenesis and lipid metabolism.
观察性和实验性数据支持绿茶对乳腺癌的潜在化学预防作用。
我们进行了一项辅助研究,使用来自一项1B期随机、安慰剂对照剂量递增试验的存档血液/尿液,该试验针对乳腺癌患者口服绿茶提取物表没食子儿茶素没食子酸酯(Polyphenon E,简称Poly E)。采用适应性试验设计,将完成辅助治疗的I - III期乳腺癌女性随机分为每日两次服用400毫克Poly E(n = 16)、600毫克(n = 11)和800毫克(n = 3)组或匹配的安慰剂组(n = 10),为期6个月。在基线、2个月、4个月和6个月时采集血液和尿液。生物学终点包括生长因子[血清肝细胞生长因子(HGF)、血管内皮生长因子(VEGF)]、脂质(血清胆固醇、甘油三酯)、氧化损伤和炎症生物标志物。
从2007年7月至2009年8月,40名女性入组,34名(26名Poly E组,8名安慰剂组)可用于生物标志物终点评估。在2个月时,Poly E组(所有剂量水平合并)与安慰剂组相比,血清HGF平均水平显著降低(-12.7%对+6.3%,P = 0.04)。这一趋势在4个月和6个月时持续存在,但不再具有统计学意义。对于Poly E组,血清VEGF在2个月时下降了11.5%(P = 0.02),在4个月时下降了13.9%(P = 0.05),但与安慰剂组相比无差异。在2个月时,Poly E组有血清胆固醇下降的趋势(P = 0.08)。其他生物标志物未观察到显著差异。
我们的研究结果表明茶多酚在生长因子信号传导、血管生成和脂质代谢方面具有潜在的作用机制。