Synergistic enhancement of anticancer effects on numerous human cancer cell lines treated with the combination of EGCG, other green tea catechins, and anticancer compounds

被引:87
作者
Fujiki, Hirota [1 ]
Sueoka, Eisaburo [1 ]
Watanabe, Tatsuro [1 ]
Suganuma, Masami [2 ]
机构
[1] Saga Univ, Dept Clin Lab Med, Fac Med, Saga 8498501, Japan
[2] Saitama Univ, Grad Sch Sci & Engn, Sakura Ku, Saitama 3388570, Japan
关键词
Apoptosis; Cancer stem cells; EGCG; GADD153; NSAID; HUMAN PROSTATE-CANCER; MALIGNANT NEUROBLASTOMA SH-SY5Y; NEGATIVE BREAST-CANCER; EPIGALLOCATECHIN GALLATE; GENE-EXPRESSION; (-)-EPIGALLOCATECHIN GALLATE; IN-VIVO; TUMOR-GROWTH; MDA-MB-231; CELLS; CARCINOMA CELLS;
D O I
10.1007/s00432-014-1899-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In 2008, we reported that 10 Japanese-size cups of green tea daily, supplemented with tablets of green tea extract (GTE), reduced the recurrence of colorectal adenoma by 51.6 % in patients after polypectomy. Based on these results, we paid special attention to Japanese cancer patients, who consume green tea every day and are administered anticancer drugs. This encouraged us to study whether the combination of green tea catechins and anticancer drugs has the potential to enhance the efficacy of the drugs. The combination of GTE and NSAIDs synergistically inhibited tumor development in rodents through the activation of the GADD153-DR5-TRAIL apoptotic pathway. Since then, this study was further extended by various investigators to the combinations of EGCG and other green tea catechins with anticancer compounds, the latter of which include NSAIDs, phytochemicals, and anticancer drugs. In order to demonstrate whether diversity of the combinations would generally induce synergistic anticancer effects on numerous human cancer cell lines, we studied the results of 42 in vitro combination experiments and the synergistic inhibition of tumor volume of 13 combination experiments using xenograft mouse models, which were previously reported by other investigators. The various combinations of EGCG and anticancer compounds induced similar synergistic anticancer effects for both in vitro and in vivo experiments, and showed an average reduction in tumor volume by 70.3 %. Considering the evidence showing that treatment with EGCG inhibited self-renewal of cancer stem cells, the combination shows a great advantage. Green tea is a cancer preventive for humans, showing a new trend of green tea catechins as synergists with anticancer compounds.
引用
收藏
页码:1511 / 1522
页数:12
相关论文
共 62 条
[1]   The development of proteasome inhibitors as anticancer drugs [J].
Adams, J .
CANCER CELL, 2004, 5 (05) :417-421
[2]   Combined inhibitory effects of green tea polyphenols and selective cyclooxygenase-2 inhibitors on the growth of human prostate cancer cells both in vitro and in vivo [J].
Adhami, Vaqar Mustafa ;
Malik, Arshi ;
Zaman, Najia ;
Sarfaraz, Sami ;
Siddiqui, Imtiaz Ahmad ;
Syed, Deeba Nadeem ;
Afaq, Farrukh ;
Pasha, Farrukh Sierre ;
Saleem, Mohammad ;
Mukhtar, Hasan .
CLINICAL CANCER RESEARCH, 2007, 13 (05) :1611-1619
[3]   Protein kinase CK2 modulates apoptosis induced by resveratrol and epigallocatechin-3-gallate in prostate cancer cells [J].
Ahmad, Kashif A. ;
Harris, Nathan H. ;
Johnson, Andrew D. ;
Lindvall, Hans C. N. ;
Wang, Guixia ;
Ahmed, Khalil .
MOLECULAR CANCER THERAPEUTICS, 2007, 6 (03) :1006-1012
[4]   Preclinical evaluation of the antitumor activity of bortezomib in combination with vitamin C or with epigallocatechin gallate, a component of green tea [J].
Bannerman, Bret ;
Xu, Ling ;
Jones, Matthew ;
Tsu, Christopher ;
Yu, Jie ;
Hales, Paul ;
Monbaliu, Johan ;
Fleming, Paul ;
Dick, Lawrence ;
Manfredi, Mark ;
Claiborne, Christopher ;
Bolen, Joseph ;
Kupperman, Erik ;
Berger, Allison .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2011, 68 (05) :1145-1154
[5]   Combinatorial effect of epigallocatechin-3-gallate and TRAIL on pancreatic cancer cell death [J].
Basu, Aruna ;
Haldar, Subrata .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2009, 34 (01) :281-286
[6]   Epigallocatechin gallate and sulforaphane combination treatment induce apoptosis in paclitaxel-resistant ovarian cancer cells through hTERT and Bcl-2 down-regulation [J].
Chen, Huaping ;
Landen, Charles N. ;
Li, Yuanyuan ;
Alvarez, Ronald D. ;
Tollefsbol, Trygve O. .
EXPERIMENTAL CELL RESEARCH, 2013, 319 (05) :697-706
[7]   Tamoxifen and epigallocatechin gallate are synergistically cytotoxic to MDA-MB-231 human breast cancer cells [J].
Chisholm, K ;
Bray, BJ ;
Rosengren, RJ .
ANTI-CANCER DRUGS, 2004, 15 (09) :889-897
[8]   (-)-Epigallocatechin-3-gallate and DZNep reduce polycomb protein level via a proteasome-dependent mechanism in skin cancer cells [J].
Choudhury, Subhasree Roy ;
Balasubramanian, Sivaprakasam ;
Chew, Yap Ching ;
Han, Bingshe ;
Marquez, Victor E. ;
Eckert, Richard L. .
CARCINOGENESIS, 2011, 32 (10) :1525-1532
[9]   Retinoids induce differentiation and downregulate telomerase activity and N-Myc to increase sensitivity to flavonoids for apoptosis in human malignant neuroblastoma SH-SY5Y cells [J].
Das, Arabinda ;
Banik, Naren L. ;
Ray, Swapan K. .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2009, 34 (03) :757-765
[10]   Celastrol and an EGCG pro-drug exhibit potent chemosensitizing activity in human leukemia cells [J].
Davenport, Andrew ;
Frezza, Michael ;
Shen, Min ;
Ge, Yubin ;
Huo, Congde ;
Chan, Tak Hang ;
Dou, Q. Ping .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2010, 25 (03) :465-470