Le Chung T, Leenders William P J, Molenaar Remco J, van Noorden Cornelis J F
a Department of Medical Biology , Academic Medical Center, University of Amsterdam, Amsterdam , The Netherlands.
b Department of Pathology, Radboudumc , Nijmegen , The Netherlands.
Nutr Cancer. 2018 Apr;70(3):317-333. doi: 10.1080/01635581.2018.1446090. Epub 2018 Mar 23.
The review discusses the effects of Epigallocatechin-3-gallate Gallate (EGCG) on glioma as a basis for future research on clinical application of EGCG. Epidemiological studies on the effects of green tea or EGCG on the risk of glioma is inconclusive due to the limited number of studies, the inclusion of all tea types in these studies, and the focus on caffeine rather than EGCG. In vivo experiments using EGCG monotherapy are inconclusive. Nevertheless, EGCG induces cell death, prevents cellular proliferation, and limits invasion in multiple glioma cell lines. Furthermore, EGCG enhances the efficacy of anti-glioma therapies, including irradiation, temozolomide, carmustine, cisplatin, tamoxifen, and TNF-related apoptosis-inducing ligand, but reduces the effect of bortezomib. Pro-drugs, co-treatment, and encapsulation are being investigated to enhance clinical applicability of EGCG. Mechanisms of actions of EGCG have been partly elucidated. EGCG has both anti-oxidant and oxidant properties. EGCG inhibits pro-survival proteins, such as telomerase, survivin, GRP78, PEA15, and P-gp. EGCG inhibits signaling of PDGFR, IGF-1R, and 67LR. EGCG reduces invasiveness of cancer cells by inhibiting the activities of various metalloproteinases, cytokines, and chemokines. Last, EGCG inhibits some NADPH-producing enzymes, thus disturbing redox status and metabolism of glioma cells. In conclusion, EGCG may be a suitable adjuvant to potentiate anti-glioma therapies.
本综述讨论了表没食子儿茶素-3-没食子酸酯(EGCG)对胶质瘤的影响,作为未来EGCG临床应用研究的基础。由于研究数量有限、这些研究纳入了所有茶类以及重点关注咖啡因而非EGCG,关于绿茶或EGCG对胶质瘤风险影响的流行病学研究尚无定论。使用EGCG单一疗法的体内实验也尚无定论。然而,EGCG可诱导细胞死亡、阻止细胞增殖并限制多种胶质瘤细胞系的侵袭。此外,EGCG可增强包括放疗、替莫唑胺、卡莫司汀、顺铂、他莫昔芬和肿瘤坏死因子相关凋亡诱导配体在内的抗胶质瘤疗法的疗效,但会降低硼替佐米的效果。正在研究前体药物、联合治疗和封装以提高EGCG的临床适用性。EGCG的作用机制已部分阐明。EGCG具有抗氧化和促氧化特性。EGCG可抑制端粒酶、生存素、葡萄糖调节蛋白78、PEA15和P-糖蛋白等促生存蛋白。EGCG可抑制血小板衍生生长因子受体(PDGFR)、胰岛素样生长因子-1受体(IGF-1R)和67LR的信号传导。EGCG通过抑制各种金属蛋白酶、细胞因子和趋化因子的活性来降低癌细胞的侵袭性。最后,EGCG可抑制一些产生烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的酶,从而扰乱胶质瘤细胞的氧化还原状态和代谢。总之,EGCG可能是增强抗胶质瘤疗法的合适佐剂。