Inhibitory effect of six green tea catechins and caffeine on the growth of four selected human tumor cell lines

被引:231
作者
Valcic, S
Timmermann, BN
Alberts, DS
Wachter, GA
Krutzsch, M
Wymer, J
Guillen, JM
机构
[1] UNIV ARIZONA,COLL PHARM,DEPT PHARMACOL & TOXICOL,TUCSON,AZ 85721
[2] UNIV ARIZONA,COLL MED,SECT HEMATOL & ONCOL,DEPT MED,TUCSON,AZ 85721
[3] UNIV ARIZONA,COLL MED,ARIZONA CANC CTR,TUCSON,AZ 85721
关键词
Camellia sinensis; catechins; green tea components; growth inhibitory activity; human tumor cell lines; isolation;
D O I
10.1097/00001813-199606000-00011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Green tea is an aqueous infusion of dried unfermented leaves of Camellia sinensis (family Theaceae) from which numerous biological activities have been reported including antimutagenic, antibacterial, hypocholesterolemic, antioxidant, antitumor and cancer preventive activities, From the aqueous-alcoholic extract of green tea leaves, six compounds (+)-gallocatechin (GC), (-)-epicatechin (EC), (-)-epigallocatechin (EGG), (-)-epicatechin gallate (EGG), (-)-epigallocatechin gallate (EGCG) and caffeine, were isolated and purified, Together with (+)-catechin, these compounds were tested against each of four human tumor cell lines (MCF-7 breast carcinoma, HT-29 colon carcinoma, A-427 lung carcinoma and UACC-375 melanoma). The three most potent green tea components against all four tumor cell lines were EGCG, GC and EGG. EGCG was the most potent of the seven green tea components against three out of the four cell lines (i.e. MCF-7 breast cancer, HT-29 colon cancer and UACC-375 melanoma), On the basis of these extensive in vitro studies, it would be of considerable interest to evaluate all three of these components in comparative preclinical in vivo animal tumor model systems before final decisions are made concerning which of these potential chemopreventive drugs should be taken into broad clinical trials.
引用
收藏
页码:461 / 468
页数:8
相关论文
共 39 条
[1]  
AGARWAL R, 1992, CANCER RES, V52, P3582
[2]   SCREENING OF TEA CLONES FOR INHIBITION OF PHIP MUTAGENICITY [J].
APOSTOLIDES, Z ;
WEISBURGER, JH .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1995, 326 (02) :219-225
[3]   MARKED ANTIMUTAGENIC POTENTIAL OF AQUEOUS GREEN TEA EXTRACTS - MECHANISM OF ACTION [J].
BUABBAS, A ;
CLIFFORD, MN ;
WALKER, R ;
IOANNIDES, C .
MUTAGENESIS, 1994, 9 (04) :325-331
[4]  
Fogh J., 1975, HUMAN TUMOR CELLS IN, P115, DOI DOI 10.1007/978-1-4757-1647-4_5
[5]  
FUJIKI H, 1994, CANCER DETECT PREV, V18, P1
[6]   IN-VITRO CULTIVATION OF HUMAN TUMORS - ESTABLISHMENT OF CELL LINES DERIVED FROM A SERIES OF SOLID TUMORS [J].
GIARD, DJ ;
AARONSON, SA ;
TODARO, GJ ;
ARNSTEIN, P ;
KERSEY, JH ;
DOSIK, H ;
PARKS, WP .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1973, 51 (05) :1417-1423
[7]   GREEN TEA COMPOSITION, CONSUMPTION, AND POLYPHENOL CHEMISTRY [J].
GRAHAM, HN .
PREVENTIVE MEDICINE, 1992, 21 (03) :334-350
[8]   SUPPRESSION OF GENOTOXICITY OF CARCINOGENS BY (-)-EPIGALLOCATECHIN GALLATE [J].
HAYATSU, H ;
INADA, N ;
KAKUTANI, T ;
ARIMOTO, S ;
NEGISHI, T ;
MORI, K ;
OKUDA, T ;
SAKATA, I .
PREVENTIVE MEDICINE, 1992, 21 (03) :370-376
[9]   CHEMOPREVENTION OF 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]-PYRIDINE (PHIP)-INDUCED MAMMARY-GLAND CARCINOGENESIS BY ANTIOXIDANTS IN F344 FEMALE RATS [J].
HIROSE, M ;
AKAGI, K ;
HASEGAWA, R ;
YAONO, M ;
SATOH, T ;
HARA, Y ;
WAKABAYASHI, K ;
ITO, N .
CARCINOGENESIS, 1995, 16 (02) :217-221
[10]   EFFECT OF FLAVAN-3-OL TANNINS PURIFIED FROM CAMELLIA-SINENSIS ON LIPID-PEROXIDATION OF RAT-HEART MITOCHONDRIA [J].
HONG, CY ;
WANG, CP ;
LO, YC ;
HSU, FL .
AMERICAN JOURNAL OF CHINESE MEDICINE, 1994, 22 (3-4) :285-292