Inhibition of conjugated fatty acids derived from safflower or perilla oil of induction and development of mammary tumors in rats induced by 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP)

被引:39
作者
Futakuchi, M
Cheng, JL
Hirose, M
Kimoto, N
Cho, YM
Iwata, T
Kasai, M
Tokudome, S
Shirai, T
机构
[1] Nagoya City Univ, Sch Med, Dept Pathol 1, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[2] Nagoya Shi Kohseiin Geriatr Hosp, Meito Ku, Nagoya, Aichi 4650055, Japan
[3] Nagoya City Univ, Dept Publ Hlth, Nagoya, Aichi, Japan
[4] Natl Inst Hlth Sci, Div Pathol, Tokyo, Japan
[5] Rinoru Oil Mills Co Ltd, Tokyo, Japan
关键词
conjugated fatty acid; chemoprevention; 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine; mammary glands;
D O I
10.1016/S0304-3835(01)00860-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemopreventive effects of conjugated fatty acids derived from safflower oil (CFA-S), which contains large amounts of conjugated linoleic acid, and from perilla oil (CFA-P) with abundant conjugated a-linolenic acid were examined in a 2-amino1-methyl-6-phenytimidazo[4,5-b]pyridine (PhIP)-induced rat mammary carcinogenesis model. Groups of 20-22 6-week-old female Sprague-Dawley (SD) rats were given eight intragastric injections of PhIP at a dose of 100 mg/kg b.w. during the initial 8 week period. Powdered basal diets containing 0.1% CFA-S or CFA-P were applied during or after PhIP treatment until week 40. In the rats receiving CFA-S or CFA-P together with PhIP treatment, retardation of mammary tumor emergence was observed until week 27. The groups given CFA-S or CFA-P after PhIP treatment, in contrast, demonstrated significant decrease in the final incidences of mammary adenocarcinomas. The indices of proliferating cell nuclear antigen positive cells in mammary adenocarcinomas were significantly reduced with both CFA-S and CFA-P in the post-initiation phase. Formation of aberrant crypt foci in the colon and basophilic foci of the pancreas due to the PhIP treatment group were not affected by CFAS or CFA-P. In a second short-term experiment, female SD rats were maintained on powdered basal diet containing 0.03% PhIP alone or together with 0.1% CFA-S or CFA-P for 4 weeks. Immunohistochemically, CFA-S and CFA-P were revealed to suppress PhIP-DNA adduct formation in the epithelial cells of mammary gland (duct and alveolar cells), colon and pancreas. These results indicated that CFA-P and CFA-S may retard development of PhIP-induced mammary tumors with inhibition of PhIP-DNA adduct formation, and decreased mammary carcinogenesis in the post-initiation period with inhibition of cell proliferation. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:131 / 139
页数:9
相关论文
共 44 条
[11]   DOSE-DEPENDENCE OF 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]-PYRIDINE (PHIP) CARCINOGENICITY IN RATS [J].
HASEGAWA, R ;
SANO, M ;
TAMANO, S ;
IMAIDA, K ;
SHIRAI, T ;
NAGAO, M ;
SUGIMURA, T ;
ITO, N .
CARCINOGENESIS, 1993, 14 (12) :2553-2557
[12]   Protection by chlorophyllin and indole-3-carbinol against 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP)-induced DNA adducts and colonic aberrant crypts in the F344 rat [J].
Herman, DG ;
Schut, HAJ ;
Davis, CD ;
Snyderwine, EG ;
Bailey, GS ;
Dashwood, RH .
CARCINOGENESIS, 1995, 16 (12) :2931-2937
[13]   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
[14]   EFFECTS OF DIETARY PERILLA OIL, SOYBEAN OIL AND SAFFLOWER OIL ON 7,12-DIMETHYLBENZ[A]ANTHRACENE (DMBA) AND 1,2-DIMETHYL-HYDRAZINE (DMH)-INDUCED MAMMARY-GLAND AND COLON CARCINOGENESIS IN FEMALE SD RATS [J].
HIROSE, M ;
MASUDA, A ;
ITO, N ;
KAMANO, K ;
OKUYAMA, H .
CARCINOGENESIS, 1990, 11 (05) :731-735
[15]   Effects of arctiin on PhIP-induced mammary, colon and pancreatic carcinogenesis in female Sprague-Dawley rats and MeIQx-induced hepatocarcinogenesis in male F344 rats [J].
Hirose, M ;
Yamaguchi, T ;
Lin, C ;
Kimoto, N ;
Futakuchi, M ;
Kono, T ;
Nishibe, S ;
Shirai, T .
CANCER LETTERS, 2000, 155 (01) :79-88
[16]  
IP C, 1985, CANCER RES, V45, P1997
[17]   Conjugated linoleic acid and linoleic acid are distinctive modulators of mammary carcinogenesis [J].
Ip, C ;
Scimeca, JA .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1997, 27 (02) :131-135
[18]  
IP C, 1994, CANCER, V74, P1050
[19]   The efficacy of conjugated linoleic acid in mammary cancer prevention is independent of the level or type of fat in the diet [J].
Ip, C ;
Briggs, SP ;
Haegele, AD ;
Thompson, HJ ;
Storkson, J ;
Scimeca, JA .
CARCINOGENESIS, 1996, 17 (05) :1045-1050
[20]  
IP C, 1991, CANCER RES, V51, P6118