Linus Pauling Institute, Oregon State University, Corvallis, OR, USA.
Pharmacol Res. 2010 Dec;62(6):457-64. doi: 10.1016/j.phrs.2010.07.010. Epub 2010 Aug 4.
Receptor tyrosine kinases (RTKs) play important roles in the control of fundamental cellular processes, influencing the balance between cell proliferation and death. RTKs have emerged as molecular targets for the treatment of various cancers. Green tea and its polyphenolic compounds, the catechins, exhibit chemopreventive and chemotherapeutic properties in many human cancer cell types, as well as in various carcinogenicity models in vivo. Epidemiological studies are somewhat less convincing, but some positive correlations have been observed. The tea catechins, including (-)-epigallocatechin-3-gallate (EGCG), have pleiotropic effects on cellular proteins and signaling pathways. This review focuses on the ability of the tea constituents to suppress RTK signaling, and summarizes the mechanisms by which EGCG and other catechins might exert their protective effects towards dysregulated RTKs in cancer cells. The findings are discussed in the context of ongoing clinical trials with RTK inhibitors, and the possibility for drug/nutrient interactions enhancing therapeutic efficacy.
受体酪氨酸激酶(RTKs)在控制基本细胞过程中发挥重要作用,影响细胞增殖和死亡之间的平衡。RTKs 已成为治疗各种癌症的分子靶标。绿茶及其多酚化合物儿茶素在许多人类癌细胞类型以及体内各种致癌模型中表现出化学预防和化学治疗特性。流行病学研究的说服力稍差,但观察到一些正相关关系。茶儿茶素,包括(-)-表没食子儿茶素-3-没食子酸酯(EGCG),对细胞蛋白和信号通路具有多种作用。本文综述了茶成分抑制 RTK 信号的能力,并总结了 EGCG 和其他儿茶素可能通过何种机制对癌细胞中失调的 RTKs 发挥保护作用。这些发现是在正在进行的 RTK 抑制剂临床试验的背景下讨论的,并探讨了药物/营养素相互作用增强治疗效果的可能性。