Absorption, metabolism, anti-cancer effect and molecular targets of epigallocatechin gallate (EGCG): An updated review

被引:377
作者
Gan, Ren-You [1 ,2 ]
Li, Hua-Bin [3 ]
Sui, Zhong-Quan [1 ]
Corke, Harold [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Agr & Biol, Dept Food Sci & Engn, Shanghai 200240, Peoples R China
[2] Univ Hong Kong, Sch Biol Sci, Hong Kong, Hong Kong, Peoples R China
[3] Sun Yat Sen Univ, Sch Publ Hlth, Dept Nutr, Guangdong Prov Key Lab Food Nutr & Hlth, Guangzhou, Guangdong, Peoples R China
关键词
Metabolism; gut microbiota; anti-cancer effect; cancer stem cells; molecular targets; nanoparticles; GREEN TEA POLYPHENOL; BREAST-CANCER CELLS; GROWTH-FACTOR RECEPTOR; HUMAN LUNG-CANCER; (-)-EPIGALLOCATECHIN-3-GALLATE INDUCES APOPTOSIS; MATRIX METALLOPROTEINASE-7 PRODUCTION; EPITHELIAL-MESENCHYMAL TRANSITION; STEM-LIKE CELLS; PROSTATE-CANCER; COLON-CANCER;
D O I
10.1080/10408398.2016.1231168
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Green tea is one of the most popular beverages in the world, especially in Asian countries. Consumption of green tea has been demonstrated to possess many health benefits, which mainly attributed to the main bioactive compound epigallocatechin gallate (EGCG), a flavone-3-ol polyphenol, in green tea. EGCG is mainly absorbed in the intestine, and gut microbiota play a critical role in its metabolism prior to absorption. EGCG exhibits versatile bioactivities, with its anti-cancer effect most attracting due to the cancer preventive effect of green tea consumption, and a great number of studies intensively investigated its anti-cancer effect. In this review, we therefore, first stated the absorption and metabolism process of EGCG, and then summarized its anti-cancer effect in vitro and in vivo, including its manifold anti-cancer actions and mechanisms, especially its anti-cancer stem cell effect, and next highlighted its various molecular targets involved in cancer inhibition. Finally, the anti-cancer effect of EGCG analogs and nanoparticles, as well as the potential cancer promoting effect of EGCG were also discussed. Understanding of the absorption, metabolism, anti-cancer effect and molecular targets of EGCG can be of importance to better utilize it as a chemopreventive and chemotherapeutic agent.
引用
收藏
页码:924 / 941
页数:18
相关论文
共 183 条
[31]   The paradox of pro-inflammatory cytokines in cancer [J].
Dinarello, Charles A. .
CANCER AND METASTASIS REVIEWS, 2006, 25 (03) :307-313
[32]   Tumor-Homing Cell-Penetrating Peptide Linked to Colloidal Mesoporous Silica Encapsulated (-)-Epigallocatechin-3-gallate as Drug Delivery System for Breast Cancer Therapy in Vivo [J].
Ding, Jie ;
Yao, Jing ;
Xue, Jingjing ;
Li, Rong ;
Bao, Bo ;
Jiang, Liping ;
Zhu, Jun-jie ;
He, Zhiwei .
ACS APPLIED MATERIALS & INTERFACES, 2015, 7 (32) :18145-18155
[33]   The Synergistic Apoptotic Interaction of Panaxadiol and Epigallocatechin Gallate in Human Colorectal Cancer Cells [J].
Du, Guang-Jian ;
Wang, Chong-Zhi ;
Qi, Lian-Wen ;
Zhang, Zhi-Yu ;
Calway, Tyler ;
He, Tong-Chuan ;
Du, Wei ;
Yuan, Chun-Su .
PHYTOTHERAPY RESEARCH, 2013, 27 (02) :272-277
[34]   Epigallocatechin Gallate (EGCG) Is the Most Effective Cancer Chemopreventive Polyphenol in Green Tea [J].
Du, Guang-Jian ;
Zhang, Zhiyu ;
Wen, Xiao-Dong ;
Yu, Chunhao ;
Calway, Tyler ;
Yuan, Chun-Su ;
Wang, Chong-Zhi .
NUTRIENTS, 2012, 4 (11) :1679-1691
[35]   The Polyphenol Epigallocatechin-3-Gallate Affects Lipid Rafts to Block Activation of the c-Met Receptor in Prostate Cancer Cells [J].
Duhon, Damian ;
Bigelow, Rebecca L. H. ;
Coleman, David T. ;
Steffan, Joshua J. ;
Yu, Chris ;
Langston, Will ;
Kevil, Christopher G. ;
Cardelli, James A. .
MOLECULAR CARCINOGENESIS, 2010, 49 (08) :739-749
[36]   Synergistic effect of curcumin on epigallocatechin gallate-induced anticancer action in PC3 prostate cancer cells [J].
Eom, Dae-Woon ;
Lee, Ji Hwan ;
Kim, Young-Joo ;
Hwang, Gwi Seo ;
Kim, Su-Nam ;
Kwak, Jin Ho ;
Cheon, Gab Jin ;
Kim, Ki Hyun ;
Jang, Hyuk-Jai ;
Ham, Jungyeob ;
Kang, Ki Sung ;
Yamabe, Noriko .
BMB REPORTS, 2015, 48 (08) :461-466
[37]   Sustained proliferation in cancer: Mechanisms and novel therapeutic targets [J].
Feitelson, Mark A. ;
Arzumanyan, Alla ;
Kulathinal, Rob J. ;
Blain, Stacy W. ;
Holcombe, Randall F. ;
Mahajna, Jamal ;
Marino, Maria ;
Martinez-Chantar, Maria L. ;
Nawroth, Roman ;
Sanchez-Garcia, Isidro ;
Sharma, Dipali ;
Saxena, Neeraj K. ;
Singh, Neetu ;
Vlachostergios, Panagiotis J. ;
Guo, Shanchun ;
Honoki, Kanya ;
Fujii, Hiromasa ;
Georgakilas, Alexandros G. ;
Bilsland, Alan ;
Amedei, Amedeo ;
Niccolai, Elena ;
Amin, Amr ;
Ashraf, S. Salman ;
Boosani, Chandra S. ;
Guha, Gunjan ;
Ciriolo, Maria Rosa ;
Aquilano, Katia ;
Chen, Sophie ;
Mohammed, Sulma I. ;
Azmi, Asfar S. ;
Bhakta, Dipita ;
Halicka, Dorota ;
Keith, W. Nicol ;
Nowsheen, Somaira .
SEMINARS IN CANCER BIOLOGY, 2015, 35 :S25-S54
[38]   Lung Cancer Inhibitory Effect of Epigallocatechin-3-Gallate Is Dependent on Its Presence in a Complex Mixture (Polyphenon E) [J].
Fu, Huijing ;
He, Jun ;
Mei, Fan ;
Zhang, Qi ;
Hara, Yukihiko ;
Ryota, Seto ;
Lubet, Ronald A. ;
Chen, Ruth ;
Chen, Da-Ren ;
You, Ming .
CANCER PREVENTION RESEARCH, 2009, 2 (06) :531-537
[39]   REDUCED RISK OF ESOPHAGEAL CANCER-ASSOCIATED WITH GREEN TEA CONSUMPTION [J].
GAO, YT ;
MCLAUGHLIN, JK ;
BLOT, WJ ;
JI, BT ;
DAI, Q ;
FRAUMENI, JF .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (11) :855-858
[40]   Epigallocatechin-3-gallate promotes apoptosis and expression of the caspase 9a splice variant in PC3 prostate cancer cells [J].
Hagen, Rachel M. ;
Chedea, Veronica S. ;
Mintoff, Christopher P. ;
Bowler, Elizabeth ;
Morse, H. Ruth ;
Ladomery, Michael R. .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2013, 43 (01) :194-200