Lamy Sylvie, Gingras Denis, Béliveau Richard
Laboratoire de Médecine Moléculaire, Centre de Cancérologie Charles-Bruneau, Hôpital Ste-Justine et Université du Québec à Montréal, Montréal, Québec H3C 3P8, Canada.
Cancer Res. 2002 Jan 15;62(2):381-5.
Vascular endothelial growth factor (VEGF) receptors (VEGFR) play a major role in tumor angiogenesis and, thus, represent attractive targets for the development of novel anticancer therapeutics. In this work, we report that green tea catechins are novel inhibitors of VEGFR-2 activity. Physiological concentrations (0.01-1 microM) of epigallocatechin-3 gallate, catechin-3 gallate, and, to a lesser extent, epicatechin-3 gallate induce a rapid and potent inhibition of VEGF-dependent tyrosine phosphorylation of VEGFR-2. The inhibition of VEGFR-2 by epigallocatechin-3 gallate was similar to that induced by Semaxanib (SU5416), a specific VEGFR-2 inhibitor. The inhibition of VEGFR-2 activity by the catechins displayed positive correlation with the suppression of in vitro angiogenesis. These observations suggest that the anticancer properties of green tea extracts may be related to their inhibition of VEGF-dependent angiogenesis.
血管内皮生长因子(VEGF)受体(VEGFR)在肿瘤血管生成中起主要作用,因此是新型抗癌治疗药物开发的有吸引力的靶点。在这项研究中,我们报告绿茶儿茶素是VEGFR - 2活性的新型抑制剂。表没食子儿茶素 - 3 - 没食子酸酯、儿茶素 - 3 - 没食子酸酯以及程度稍轻的表儿茶素 - 3 - 没食子酸酯的生理浓度(0.01 - 1 microM)可快速且有效地抑制VEGFR - 2的VEGF依赖性酪氨酸磷酸化。表没食子儿茶素 - 3 - 没食子酸酯对VEGFR - 2的抑制作用与特异性VEGFR - 2抑制剂司马沙尼(SU5416)诱导的抑制作用相似。儿茶素对VEGFR - 2活性的抑制与体外血管生成的抑制呈正相关。这些观察结果表明,绿茶提取物的抗癌特性可能与其对VEGF依赖性血管生成的抑制作用有关。