Effects of dietary beta-carotene and selenium on initiation and promotion of pancreatic carcinogenesis in azaserine-treated rats

被引:23
作者
Appel, MJ [1 ]
Woutersen, RA [1 ]
机构
[1] TNO,NUTR & FOOD RES INST,DEPT GEN TOXICOL,DIV TOXICOL,NL-3700 AJ ZEIST,NETHERLANDS
关键词
D O I
10.1093/carcin/17.7.1411
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the present study the effects of 0.1 or 1.0 g beta-carotene/kg diet (L beta C or H beta C) and 1.0 mg or 2.5 mg selenium/kg diet (LSel or HSel), as well as combinations of the respective low and high concentrations of beta-carotene and selenium (LMix or HMix) on the initiation/early promotion phase or on the late promotion phase of pancreatic carcinogenesis in azaserine-treated rats, were investigated using cell proliferation and volumetric data of atypical acinar cell foci (AACF) as parameters, The present results indicate chemopreventive effects of dietary selenium, dietary beta-carotene and of their combination on the development of acinar pancreatic lesions induced in rats by azaserine, The inhibitory effect was most pronounced when beta-carotene and/or selenium were added to the diets during the late promotion phase of the carcinogenic process, although inhibition was also observed with these compounds when they were added to the diets during the first 5 weeks of the study only (initiation/early promotion phase), Neither in the initiation/early promotion phase nor in the late promotion phase was a dose-related trend observed, The multiplicities of AACF with a diameter over 1.0 mm and of carcinomas in situ (CIS), as well as the incidence of CIS were not significantly different among the groups, However, in the late promotion experiment a dose-related decline in multiplicity could be observed in the selenium supplemented groups and in the groups receiving combinations of beta-carotene and selenium, Cell proliferation in azaserine-induced AACF, as estimated by the bromodeoxyuridine (BrdU) labeling index, was significantly higher in H beta C, HSel, LMix and HMix groups (initiation/early promotion phase) as well as in H beta C, LSel, HSel, LMix and HMix groups (late promotion phase) than in high fat controls, From the present results it can be concluded that: (i) beta-carotene and selenium have inhibitory effects on pancreatic carcinogenesis induced in rats by azaserine; (ii) the most clear effects were observed when selenium was given as such, or in combination with beta-carotene during the late promotion phase; and (iii) beta-carotene and selenium stimulate cell proliferation in AACF.
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页码:1411 / 1416
页数:6
相关论文
共 34 条
[1]   EFFECT OF BETA-CAROTENE AND WHEAT BRAN FIBER ON COLONIC ABERRANT CRYPT AND TUMOR-FORMATION IN RATS EXPOSED TO AZOXYMETHANE AND HIGH DIETARY-FAT [J].
ALABASTER, O ;
TANG, ZC ;
FROST, A ;
SHIVAPURKAR, N .
CARCINOGENESIS, 1995, 16 (01) :127-132
[2]  
ALAM B S, 1987, Nutrition and Cancer, V9, P93
[3]   Dietary fish oil (MaxEPA) enhances pancreatic carcinogenesis in azaserine-treated rats [J].
Appel, MJ ;
Woutersen, RA .
BRITISH JOURNAL OF CANCER, 1996, 73 (01) :36-43
[4]   INHIBITORY EFFECTS OF MICRONUTRIENTS ON PANCREATIC CARCINOGENESIS IN AZASERINE-TREATED RATS [J].
APPEL, MJ ;
ROVERTS, G ;
WOUTERSEN, RA .
CARCINOGENESIS, 1991, 12 (11) :2157-2161
[5]   SHORT-TERM (6-WEEK) ORAL TOXICITY STUDY OF SELENIUM IN SYRIAN-HAMSTERS [J].
BEEMS, RB ;
VANBEEK, L .
FOOD AND CHEMICAL TOXICOLOGY, 1985, 23 (10) :945-947
[6]   ENHANCEMENT OF BOP-INDUCED PANCREATIC CARCINOGENESIS IN SELENIUM-FED SYRIAN GOLDEN-HAMSTERS UNDER SPECIFIC DIETARY CONDITIONS [J].
BIRT, DF ;
JULIUS, AD ;
RUNICE, CE ;
WHITE, LT ;
LAWSON, T ;
POUR, PM .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1988, 11 (01) :21-33
[7]   SEROLOGIC PRECURSORS OF CANCER - SERUM MICRONUTRIENTS AND THE SUBSEQUENT RISK OF PANCREATIC-CANCER [J].
BURNEY, PGJ ;
COMSTOCK, GW ;
MORRIS, JS .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1989, 49 (05) :895-900
[8]   SUBCHRONIC TOXICITY OF BENZYL SELENOCYANATE AND 1,4-PHENYLENEBIS(METHYLENE)SELENOCYANATE IN F344 RATS [J].
CONAWAY, CC ;
UPADHYAYA, P ;
MESCHTER, CL ;
KURTZKE, C ;
MARCUS, LA ;
ELBAYOUMY, K .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1992, 19 (04) :563-574
[9]  
CURPHEY TJ, 1988, PANCREAS, V1, P36
[10]  
HEINONEN OP, 1994, NEW ENGL J MED, V330, P1029