Isothiocyanates and freeze-dried strawberries as inhibitors of esophageal cancer

被引:50
作者
Stoner, GD
Kresty, LA
Carlton, PS
Siglin, JC
Morse, MA
机构
[1] Ohio State Univ, Sch Publ Hlth, Div Environm Hlth Sci, Columbus, OH 43210 USA
[2] Ohio State Univ, CHRI, Ctr Comprehens Canc, Columbus, OH 43210 USA
关键词
rat; esophagus; isothiocyanate; phenylpropyl isothiocyanate (PPITC); strawberries; N-nitrosomethylbenzylamine (NMBA); chemoprevention;
D O I
10.1093/toxsci/52.suppl_1.95
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
A group of arylalkyl isothiocyanates were tested for their abilities to inhibit tumorigenicity and DNA methylation induced by the esophageal-specific carcinogen, N-nitrosomethylbenzylamine (NMBA) in the F344 rat esophagus. Phenylpropyl isothiocyanate (PPITC) was more potent than either phenylethyl isothiocyanate (PEITC) or benzyl isothiocyanate (BITC). Phenylbutyl isothiocyanate (PBITC), however, had a lesser inhibitory effect on esophageal tumorigenesis, and phenylhexyl isothiocyanate (PHITC) actually enhanced esophageal tumorigenesis. Thus, the two- and three-carbon isothiocyanates were more effective inhibitors of NMBA-esophageal carcinogenesis than the longer chain isothiocyanates. The effects of the isothiocyanates on tumorigenesis were well correlated as to their effects on DNA adduct formation. The most likely mechanism of inhibition of tumorigenesis by these isothiocyanates is via inhibition of the cytochrome P450 enzymes responsible for the metabolic activation of NMBA in rat esophagus. A freeze-dried strawberry preparation was also evaluated for its ability to inhibit NMBA-esophageal tumorigenesis. It proved to be an effective inhibitor, although not as potent as either PEITC or PPITC. The inhibitory effect of the berries could not be attributed solely to the content of the chemopreventive agent, ellagic acid, in the berries.
引用
收藏
页码:95 / 100
页数:6
相关论文
共 23 条
  • [11] MORSE MA, 1991, CANCER RES, V51, P1846
  • [12] EFFECTS OF ALKYL CHAIN-LENGTH ON THE INHIBITION OF NNK-INDUCED LUNG NEOPLASIA IN A/J MICE BY ARYLALKYL ISOTHIOCYANATES
    MORSE, MA
    EKLIND, KI
    AMIN, SG
    HECHT, SS
    CHUNG, FL
    [J]. CARCINOGENESIS, 1989, 10 (09) : 1757 - 1759
  • [13] MORSE MA, 1997, CANC LETT, V112, P199
  • [14] PARKIN DM, 1984, B WORLD HEALTH ORGAN, V62, P163, DOI 10.1139/b84-027
  • [15] SEBTI SM, 1985, CANCER RES, V45, P1594
  • [16] Stoner Gary D., 1995, P141
  • [17] Inhibition of N′-nitrosonornicotine-induced esophageal tumorigenesis by 3-phenylpropyl isothiocyanate
    Stoner, GD
    Adams, C
    Kresty, LA
    Amin, SG
    Desai, D
    Hecht, SS
    Murphy, SE
    Morse, MA
    [J]. CARCINOGENESIS, 1998, 19 (12) : 2139 - 2143
  • [18] STONER GD, 1991, CANCER RES, V51, P2063
  • [19] ENHANCEMENT OF ESOPHAGEAL CARCINOGENESIS IN MALE F344 RATS BY DIETARY PHENYLHEXYL ISOTHIOCYANATE
    STONER, GD
    SIGLIN, JC
    MORSE, MA
    DESAI, DH
    AMIN, SG
    KRESTY, LA
    TOBUREN, AL
    HEFFNER, EM
    FRANCIS, DJ
    [J]. CARCINOGENESIS, 1995, 16 (10) : 2473 - 2476
  • [20] Isothiocyanates and plant polyphenols as inhibitors of lung and esophageal cancer
    Stoner, GD
    Morse, MA
    [J]. CANCER LETTERS, 1997, 114 (1-2) : 113 - 119