EGCG, GREEN TEA POLYPHENOLS AND THEIR SYNTHETIC ANALOGS AND PRODRUGS FOR HUMAN CANCER PREVENTION AND TREATMENT

被引:174
作者
Chen, Di [1 ,2 ,3 ,4 ]
Wan, Sheng Biao [5 ]
Yang, Huanjie [1 ,2 ,3 ,4 ,6 ]
Yuan, Jian [5 ]
Chan, Tak Hang [7 ]
Dou, Q. Ping [1 ,2 ,3 ,4 ]
机构
[1] Wayne State Univ, Sch Med, Dev Therapeut Program, Barbara Ann Karmanos Canc Inst, Detroit, MI 48202 USA
[2] Wayne State Univ, Dept Oncol, Detroit, MI USA
[3] Wayne State Univ, Dept Pathol, Detroit, MI USA
[4] Wayne State Univ, Dept Pharmacol, Sch Med, Detroit, MI USA
[5] Ocean Univ China, Key Lab Marine Drugs, Chinese Minist Educ, Sch Med & Pharm, Qingdao, Peoples R China
[6] Harbin Inst Technol, Dept Life Sci & Engn, Harbin 150006, Peoples R China
[7] McGill Univ, Dept Chem, Montreal, PQ, Canada
来源
ADVANCES IN CLINICAL CHEMISTRY, VOL 53 | 2011年 / 53卷
关键词
DOWNSTREAM SIGNALING PATHWAYS; RENAL-CELL CARCINOMA; (-)-EPIGALLOCATECHIN GALLATE; LUNG-CANCER; PROSTATE-CANCER; BREAST-CANCER; PROTEASOME INHIBITORS; IN-VITRO; EPIGALLOCATECHIN-3-GALLATE EGCG; MOLECULAR-MECHANISMS;
D O I
10.1016/S0065-2423(11)53007-0
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Cancer-preventive effects of tea polyphenols, especially epigallocatechin-3-gallate (EGCG), have been demonstrated by epidemiological, preclinical, and clinical studies. Green tea polyphenols such as EGCG have the potential to affect multiple biological pathways, including gene expression, growth factor-mediated pathways, the mitogen-activated protein kinase-dependent pathway, and the ubiquitin/proteasome degradation pathway. Therefore, identification of the molecular targets of EGCG should greatly facilitate a better understanding of the mechanisms underlying its anticancer and cancer-preventive activities. Performing structure-activity relationship (SAR) studies could also greatly enhance the discovery of novel tea polyphenol analogs as potential anticancer and cancer-preventive agents. In this chapter, we review the relevant literature as it relates to the effects of natural and synthetic green tea polyphenols and EGCG analogs on human cancer cells and their potential molecular targets as well as their antitumor effects. We also discuss the implications of green tea polyphenols in cancer prevention.
引用
收藏
页码:155 / 177
页数:23
相关论文
共 131 条
[1]   Development of the proteasome inhibitor PS-341 [J].
Adams, J .
ONCOLOGIST, 2002, 7 (01) :9-16
[2]   Oral consumption of green tea polyphenols inhibits insulin-like growth factor-i-induced signaling in an autochthonous mouse model of prostate cancer [J].
Adhami, VM ;
Siddiqui, IA ;
Ahmad, N ;
Gupta, S ;
Mukhtar, H .
CANCER RESEARCH, 2004, 64 (23) :8715-8722
[3]   Novel dipeptidyl proteasome inhibitors overcome Bcl-2 protective function and selectively accumulate the cyclin-dependent kinase inhibitor p27 and induce apoptosis in transformed, but not normal, human fibroblasts [J].
An, B ;
Goldfarb, RH ;
Siman, R ;
Dou, QP .
CELL DEATH AND DIFFERENTIATION, 1998, 5 (12) :1062-1075
[4]   Inhibition of HuR and MMP-9 expression in macrophage-differentiated HL-60 myeloid leukemia cells by green tea polyphenol EGCg [J].
Annabi, Borhane ;
Currie, Jean-Christophe ;
Moghrabi, Albert ;
Beliveau, Richard .
LEUKEMIA RESEARCH, 2007, 31 (09) :1277-1284
[5]   Epigenetic gene silencing in cancer - a mechanism for early oncogenic pathway addiction? [J].
Baylin, SB ;
Ohm, JE .
NATURE REVIEWS CANCER, 2006, 6 (02) :107-116
[6]   Chemoprevention of human prostate cancer by oral administration of green tea catechins in volunteers with high-grade prostate intraepithelial neoplasia: A preliminary report from a one-year proof-of-principle study [J].
Bettuzzi, S ;
Brausi, M ;
Rizzi, F ;
Castagnetti, G ;
Peracchia, G ;
Corti, A .
CANCER RESEARCH, 2006, 66 (02) :1234-1240
[7]  
Bettuzzi S, 2007, POL J VET SCI, V10, P57
[8]   Differential responses of skin cancer-chemopreventive agents silibinin, quercetin, and epigallocatechin 3-gallate on mitogenic signaling and cell cycle regulators in human epidermoid carcinoma A431 cells [J].
Bhatia, N ;
Agarwal, C ;
Agarwal, R .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 2001, 39 (02) :292-299
[9]  
Chen D, 2008, HISTOL HISTOPATHOL, V23, P487, DOI 10.14670/HH-23.487
[10]   Indoleamine 2,3-Dioxygenase, an Immunomodulatory Protein, Is Suppressed by (-)-Epigallocatechin-3-gallate via Blocking of γ-Interferon-Induced JAK-PKC-δ-STAT1 Signaling in Human Oral Cancer Cells [J].
Cheng, Chieh-Wen ;
Shieh, Po-Chuen ;
Lin, Ying-Chao ;
Chen, Yi-Jen ;
Lin, Yu-Huei ;
Kuo, Daih-Huang ;
Liu, Jah-Yao ;
Kao, Jung-Yie ;
Kao, Ming-Ching ;
Way, Tzong-Der .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2010, 58 (02) :887-894