Dipartimento di Scienze Farmacologiche, Biologiche e Chimiche Applicate, Università di Parma, Viale G.P. Usberti 27a, 43124 Parma, Italy.
Pharmacol Res. 2011 Nov;64(5):464-70. doi: 10.1016/j.phrs.2011.06.008. Epub 2011 Jul 1.
The Eph tyrosine kinase receptors and their ephrin ligands play a central role in several human cancers and their deregulated expression or function promotes tumorigenesis, inducing aggressive tumor phenotypes. Green tea extracts (GTE) have been recently found to inhibit Eph-kinase phosphorylation. In order to evaluate the potential contribution of edible and medicinal plants on EphA2-ephrinA1 modulation, 133 commercially available plant extracts used as food supplements, essential and fixed oils were screened with an ELISA-based binding assay. Nine plant extracts, rich of polyphenols, reversibly inhibited binding in a dose-dependent manner (IC₅₀ 0.83-24 μg/ml). Functional studies on PC3 prostate adenocarcinoma cells revealed that active extracts antagonized ephrinA1-Fc-induced EphA2-phosphorylation at non-cytotoxic concentrations (IC₅₀ 0.31-11.3 μg/ml) without interfering with EGF-induced EGFR activation, suggesting a specific effect. These findings could furnish an interesting starting point regarding the potential relationship between diet, edible plant secondary metabolites and Eph-ephrin system, suggesting their possible involvement in cancer development modulation.
Eph 酪氨酸激酶受体及其配体在几种人类癌症中起着核心作用,其表达或功能失调会促进肿瘤发生,诱导侵袭性肿瘤表型。最近发现绿茶提取物 (GTE) 可抑制 Eph-激酶磷酸化。为了评估食用和药用植物对 EphA2-ephrinA1 调节的潜在贡献,我们使用基于 ELISA 的结合测定法筛选了 133 种市售用作食品补充剂、精油和固定油的植物提取物。9 种富含多酚的植物提取物以剂量依赖性方式可逆地抑制结合(IC₅₀ 0.83-24μg/ml)。对 PC3 前列腺腺癌细胞的功能研究表明,活性提取物在非细胞毒性浓度(IC₅₀ 0.31-11.3μg/ml)下拮抗 EphrinA1-Fc 诱导的 EphA2 磷酸化,而不干扰 EGF 诱导的 EGFR 激活,提示具有特异性作用。这些发现为饮食、食用植物次生代谢物和 Eph-ephrin 系统之间的潜在关系提供了一个有趣的起点,提示它们可能参与癌症发展的调节。