Epicatechins purified from green tea (Camellia sinensis) differentially suppress growth of gender-dependent human cancer cell lines

被引:73
作者
Ravindranath, Mepur H.
Saravanan, Thiruverkadu S.
Monteclaro, Clarence C.
Presser, Naftali
Ye, Xing
Selvan, Senthamil R.
Brosman, Stanley
机构
[1] John Wayne Canc Inst, Dept Glycoimmunotherapy, Santa Monica, CA 90404 USA
[2] Hoag Mem Hosp, Cell Biol Lab, Hoag Canc Ctr, Newport Beach, CA USA
[3] Pacific Clin Res, Santa Monica, CA USA
关键词
green tea; epicatechin (EC); epigallocatechin (EGC); EC 3-gallate (ECG); EGC 3-gallate (EGCG); organ-confined; metastatic; prostate cancer; epithelial ovarian cancer; viability; doubling time; 50% inhibitory concentration (IC50);
D O I
10.1093/ecam/nel003
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
The anticancer potential of catechins derived from green tea is not well understood, in part because catechin-related growth suppression and/or apoptosis appears to vary with the type and stage of malignancy as well as with the type of catechin. This in vitro study examined the biological effects of epicatechin (EC), epigallocatechin (EGC), EC 3-gallate (ECG) and EGC 3-gallate (EGCG) in cell lines from human gender-specific cancers. Cell lines developed from organ-confined (HH870) and metastatic (DU145) prostate cancer, and from moderately (HH450) and poorly differentiated (HH639) epithelial ovarian cancer were grown with or without EC, EGC, ECG or EGCG. When untreated cells reached confluency, viability and doubling time were measured for treated and untreated cells. Whereas EC treatment reduced proliferation of HH639 cells by 50%, EGCG suppressed proliferation of all cell lines by 50%. ECG was even more potent: it inhibited DU145, HH870, HH450 and HH639 cells at concentrations of 24, 27, 29 and 30 mu M, whereas EGCG inhibited DU145, HH870, HH450 and HH639 cells at concentrations 89, 45, 62 and 42 mu M. When compared with EGCG, ECG more effectively suppresses the growth of prostate cancer and epithelial ovarian cancer cell lines derived from tumors of patients with different stages of disease.
引用
收藏
页码:237 / 247
页数:11
相关论文
共 43 条
[21]   Involvement of protein tyrosine phosphorylation in the effect of green tea polyphenols on Ehrlich ascites tumor cells in vitro [J].
Kennedy, DO ;
Nishimura, S ;
Hasuma, T ;
Yano, Y ;
Otani, S ;
Matsui-Yuasa, I .
CHEMICO-BIOLOGICAL INTERACTIONS, 1998, 110 (03) :159-172
[22]   Activity-guided fractionation of green tea extract with antiproliferative activity against human stomach cancer cells [J].
Kinjo, J ;
Nagao, T ;
Tanaka, T ;
Nonaka, G ;
Okawa, M ;
Nohara, T ;
Okabe, H .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2002, 25 (09) :1238-1240
[23]   Tea catechins inhibit angiogenesis endothelial cell growth, migration in vitro, measured by human and tube formation, through inhibition of VEGF receptor binding [J].
Kondo, T ;
Ohta, T ;
Igura, K ;
Hara, Y ;
Kaji, K .
CANCER LETTERS, 2002, 180 (02) :139-144
[24]   Delivery of tea polyphenols to the oral cavity by green tea leaves and black tea extract [J].
Lee, MJ ;
Lambert, JD ;
Prabhu, S ;
Meng, XF ;
Lu, H ;
Maliakal, P ;
Ho, CT ;
Yang, CS .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2004, 13 (01) :132-137
[25]  
Liang Gang, 2004, Ai Zheng, V23, P401
[26]   Chemopreventive effects of tea extracts and various components on human pancreatic and prostate tumor cells in vitro [J].
Lyn-Cook, BD ;
Rogers, T ;
Yan, Y ;
Blann, EB ;
Kadlubar, FF ;
Hammons, GJ .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1999, 35 (01) :80-86
[27]   Effects of tea polyphenols on the invasion and matrix metalloproteinases activities of human fibrosarcoma HT1080 cells [J].
Maeda-Yamamoto, M ;
Kawahara, H ;
Tahara, N ;
Tsuji, K ;
Hara, Y ;
Isemura, M .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1999, 47 (06) :2350-2354
[28]   INHIBITORY EFFECT OF TEA CATECHINS ON COLLAGENASE ACTIVITY [J].
MAKIMURA, M ;
HIRASAWA, M ;
KOBAYASHI, K ;
INDO, J ;
SAKANAKA, S ;
TAGUCHI, T ;
OTAKE, S .
JOURNAL OF PERIODONTOLOGY, 1993, 64 (07) :630-636
[29]   Green tea in chemoprevention of cancer [J].
Mukhtar, H ;
Ahmad, N .
TOXICOLOGICAL SCIENCES, 1999, 52 (02) :111-117
[30]  
Muramatsu K., 2002, HLTH SCI TEA, P52