Inhibitory effects of topical application of low doses of curcumin on 12-O-tetradecanoylphorbol-13-acetate-induced tumor promotion and oxidized DNA bases in mouse epidermis

被引:137
作者
Huang, MT
Ma, W
Yen, P
Xie, JG
Han, JK
Frenkel, K
Grunberger, D
Conney, AH
机构
[1] NYU, MED CTR, DEPT ENVIRONM MED, NEW YORK, NY 10016 USA
[2] COLUMBIA UNIV COLL PHYS & SURG, INST CANC RES, NEW YORK, NY 10032 USA
关键词
D O I
10.1093/carcin/18.1.83
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The effects of topical applications of very low doses of curcumin (the major yellow pigment in turmeric and the Indian food curry) on 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced oxidation of DNA bases in the epidermis and on tumor promotion in mouse skin were investigated, CD-1 mice were treated topically with 200 mnol of 7,12-dimethylbenz[a]anthracene followed one week later by 5 nmol of TPA alone or together with 1, 10, 100 or 3000 mmol of curcumin twice a week for 20 weeks. Curcumin-mediated effects on TPA-induced formation of the oxidized DNA base 5-hydroxymethyl-2'-deoxyuridine (HMdU) and tumor formation were determined. All dose levels of curcumin inhibited the mean values of TPA-induced HMdU formation in epidermal DNA (62-77% inhibition), but only the two highest doses of curcumin strongly inhibited TPA-induced tumor promotion (62-79% inhibition of tumors per mouse and tumor volume per mouse), In a second experiment, topical application of 20 or 100 mnol (but not 10 mmol) of curcumin together with 5 mmol TPA twice a week for 18 weeks markedly inhibited TPA-induced tumor promotion, Curcumin had a strong inhibitory effect on DNA and RNA synthesis (IC50 = 0.5-1 mu M) in cultured HeLa cells, but there was little or no effect on protein synthesis.
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页码:83 / 88
页数:6
相关论文
共 48 条
[1]   PHARMACOLOGY OF CURCUMA-LONGA [J].
AMMON, HPT ;
WAHL, MA .
PLANTA MEDICA, 1991, 57 (01) :1-7
[2]  
ARMSTAD PA, 1992, CANCER RES, V52, P3952
[3]   Growth control of lung cancer by interruption of 5-lipoxygenase-mediated growth factor signaling [J].
Avis, IM ;
Jett, M ;
Boyle, T ;
Vos, MD ;
Moody, T ;
Treston, AM ;
Martinez, A ;
Mulshine, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (03) :806-813
[4]  
BACON E, 1979, CAN PHARM J, V112, P340
[5]  
BASS DA, 1983, J IMMUNOL, V130, P1910
[6]   INHIBITION OF TUMOR-NECROSIS-FACTOR BY CURCUMIN, A PHYTOCHEMICAL [J].
CHAN, MMY .
BIOCHEMICAL PHARMACOLOGY, 1995, 49 (11) :1551-1556
[7]   EFFECTS OF 3 DIETARY PHYTOCHEMICALS FROM TEA, ROSEMARY AND TURMERIC ON INFLAMMATION-INDUCED NITRITE PRODUCTION [J].
CHAN, MMY ;
HO, CT ;
HUANG, HI .
CANCER LETTERS, 1995, 96 (01) :23-29
[8]  
CHOPRA RN, 1958, INDIGENOUS DRUGS IND, P325
[9]   INVOLVEMENT OF REACTIVE OXYGEN INTERMEDIATES IN THE INDUCTION OF C-JUN GENE-TRANSCRIPTION BY IONIZING-RADIATION [J].
DATTA, R ;
HALLAHAN, DE ;
KHARBANDA, SM ;
RUBIN, E ;
SHERMAN, ML ;
HUBERMAN, E ;
WEICHSELBAUM, RR ;
KUFE, DW .
BIOCHEMISTRY, 1992, 31 (35) :8300-8306
[10]   INHIBITION OF 5-HYDROXY-EICOSATETRAENOIC ACID (5-HETE) FORMATION IN INTACT HUMAN-NEUTROPHILS BY NATURALLY-OCCURRING DIARYLHEPTANOIDS - INHIBITORY ACTIVITIES OF CURCUMINOIDS AND YAKUCHINONES [J].
FLYNN, DL ;
RAFFERTY, MF ;
BOCTOR, AM .
PROSTAGLANDINS LEUKOTRIENES AND MEDICINE, 1986, 22 (03) :357-360