Protective effects of benzyl isothiocyanate and sulforaphane but not resveratrol against initiation of pancreatic carcinogenesis in hamsters

被引:77
作者
Kuroiwa, Yuichi [1 ]
Nishikawa, Akiyoshi [1 ]
Kitamura, Yasuki [1 ]
Kanki, Keita [1 ]
Ishii, Yuji [1 ]
Umemura, Takashi [1 ]
Hirose, Masao [1 ]
机构
[1] Natl Inst Hlth Sci, Div Pathol, Setagaya Ku, Tokyo 1588501, Japan
关键词
pancreatic carcinogenesis; hamster; benzyl isothiocyanate; sulforaphane; resveratrol;
D O I
10.1016/j.canlet.2005.10.028
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Potential chemopreventive effects of naturally occurring agents were investigated using a new 16-week medium-term pancreatic carcinogenesis models in hamsters. Male 6-week-old Syrian hamsters were subcutaneously injected with 10 mg/kg body weight N-nitrosobis(2-oxopropyl)amine (BOP) four times within a week, and fed a diet supplemented with 80 ppm benzyl isothiocyanate (BITC), 80 ppm sulforaphane (SFN) or 10 ppm resveratrol (RES) during the initiation or post-initiation stages. For the initiation stage, each chemical was given for 3 weeks including 1 week before and after the BOP injections. With post-initiation exposure, the groups were changed from basal diet 1 week after the last BOP injection, and then fed each chemical for 14 weeks. All the animals were sacrificed after 16 weeks. The multiplicities of combined pancreatic lesions including atypical hyperplasias and adenocarcinomas were significantly decreased by BITC and SFN given in the initiation but not the post-initiation stage. On the other hand, RES, a naturally occurring inhibitor of cyclooxygenase-2 (COX-2) reported chemopreventive effects, failed to show significant effects on pancreatic carcinogenesis in either the initiation or post-initiation stages. Our data suggest that the naturally occurring isothiocyanates BITC and SFN can block BOP-initiation of hamster pancreatic carcinogenesis. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:275 / 280
页数:6
相关论文
共 37 条
[1]   A CASE-CONTROL STUDY OF DIET AND CANCER OF THE PANCREAS [J].
BAGHURST, PA ;
MCMICHAEL, AJ ;
SLAVOTINEK, AH ;
BAGHURST, KI ;
BOYLE, P ;
WALKER, AM .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1991, 134 (02) :167-179
[2]  
Banerjee S, 2002, CANCER RES, V62, P4945
[3]  
Cal C., 2003, Current Medicinal Chemistry - Anti-Cancer Agents, V3, P77, DOI 10.2174/1568011033353443
[4]   Chemoprevention of colonic aberrant crypt foci in Fischer rats by sulforaphane and phenethyl isothiocyanate [J].
Chung, FL ;
Conaway, CC ;
Rao, CV ;
Reddy, BS .
CARCINOGENESIS, 2000, 21 (12) :2287-2291
[5]   INTAKE OF FOODS AND NUTRIENTS AND CANCER OF THE EXOCRINE PANCREAS - A POPULATION-BASED CASE-CONTROL STUDY IN THE NETHERLANDS [J].
DEMESQUITA, HBB ;
MAISONNEUVE, P ;
RUNIA, S ;
MOERMAN, CJ .
INTERNATIONAL JOURNAL OF CANCER, 1991, 48 (04) :540-549
[6]  
Ding Xian-Zhong, 2002, Pancreas, V25, pe71, DOI 10.1097/00006676-200211000-00024
[7]   Biochemistry of cyclooxygenase (COX)-2 inhibitors and molecular pathology of COX-2 in neoplasia [J].
Fosslien, E .
CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 2000, 37 (05) :431-502
[8]   A cyclooxygenase-2 inhibitor, nimesulide, inhibits postinitiation phase of N-nitrosobis(2-oxopropyl)amine-induced pancreatic carcinogenesis in hamsters [J].
Furukawa, F ;
Nishikawa, A ;
Lee, IS ;
Kanki, K ;
Umemura, T ;
Okazaki, K ;
Kawamori, T ;
Wakabayashi, K ;
Hirose, M .
INTERNATIONAL JOURNAL OF CANCER, 2003, 104 (03) :269-273
[9]   Inhibition of carcinogenesis by isothiocyanates [J].
Hecht, SS .
DRUG METABOLISM REVIEWS, 2000, 32 (3-4) :395-411
[10]   Nitric oxide-donating nonsteroidal anti-inflammatory drugs inhibit the growth of various cultured human cancer cells: Evidence of a tissue type-independent effect [J].
Kashfi, K ;
Ryann, Y ;
Qiao, LL ;
Williams, JL ;
Chen, J ;
Del Soldato, P ;
Traganos, F ;
Rigas, B .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 303 (03) :1273-1282