ROLE OF ACETYLATION IN COLORECTAL-CANCER

被引:62
作者
MINCHIN, RF [1 ]
KADLUBAR, FF [1 ]
ILETT, KF [1 ]
机构
[1] NATL CTR TOXICOL RES,JEFFERSON,AR 72079
来源
MUTATION RESEARCH | 1993年 / 290卷 / 01期
关键词
COLORECTAL CANCER; ACETYLATION PHENOTYPE; HETEROCYCLIC AMINES;
D O I
10.1016/0027-5107(93)90030-J
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Acetylator phenotype is a common genetic trait in humans as well as other mammals. It results from the presence of several mutations in one of the genes encoding for arylamine N-acetyltransferase. The polymorphism has been associated with several disease states including colorectal cancer. Several epidemiological studies suggest that rapid acetylators are more susceptible to colorectal cancer than slow acetylators. Moreover, individuals that are both rapid acetylators and exhibit a high cytochrome P450 1A2 activity appear to have an even higher risk of colorectal cancer. These observations not only suggest an interesting genetic link to non-familial colon cancer but also suggest that carcinogens that are activated by N-acetyltransferase and cytochrome P450 1A2 may contribute to the etiology of this disease. Heterocyclic amines present in cooked food such as ''well done'' red meat are carcinogenic in experimental animals forming tumours in several target tissues including the small intestines. We have shown that human polymorphic N-acetyltransferase is present in human colon tissue and that it is capable of activating several heterocyclic amine carcinogens present in cooked food. These studies provide good circumstantial evidence that rapid acetylators may be predisposed to colorectal cancer.
引用
收藏
页码:35 / 42
页数:8
相关论文
共 32 条
  • [1] FORMATION OF A GLUTATHIONE CONJUGATE AND A SEMISTABLE TRANSPORTABLE GLUCURONIDE CONJUGATE OF N2-OXIDIZED SPECIES OF 2-AMINO-1-METHYL-6-PHENYLIMIDAZO[4,5-B]PYRIDINE (PHIP) IN RAT-LIVER
    ALEXANDER, J
    WALLIN, H
    ROSSLAND, OJ
    SOLBERG, KE
    HOLME, JA
    BECHER, G
    ANDERSSON, R
    GRIVAS, S
    [J]. CARCINOGENESIS, 1991, 12 (12) : 2239 - 2245
  • [2] Beland FA, 1990, HDB EXPT PHARM CHEM, P267
  • [3] BELL DA, 1993, IN PRESS MOL HUMAN G
  • [4] MOLECULAR MECHANISM OF SLOW ACETYLATION OF DRUGS AND CARCINOGENS IN HUMANS
    BLUM, M
    DEMIERRE, A
    GRANT, DM
    HEIM, M
    MEYER, UA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (12) : 5237 - 5241
  • [5] HUMAN ARYLAMINE N-ACETYLTRANSFERASE GENES - ISOLATION, CHROMOSOMAL LOCALIZATION, AND FUNCTIONAL EXPRESSION
    BLUM, M
    GRANT, DM
    MCBRIDE, W
    HEIM, M
    MEYER, UA
    [J]. DNA AND CELL BIOLOGY, 1990, 9 (03) : 193 - 203
  • [6] HUMAN CYTOCHROME P-450PA (P-450IA2), THE PHENACETIN O-DEETHYLASE, IS PRIMARILY RESPONSIBLE FOR THE HEPATIC 3-DEMETHYLATION OF CAFFEINE AND N-OXIDATION OF CARCINOGENIC ARYLAMINES - (AROMATIC-AMINES HETEROCYCLIC AMINES CARCINOGEN METABOLISM)
    BUTLER, MA
    IWASAKI, M
    GUENGERICH, FP
    KADLUBAR, FF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (20) : 7696 - 7700
  • [7] DETERMINATION OF CYP1A2 AND NAT2 PHENOTYPES IN HUMAN-POPULATIONS BY ANALYSIS OF CAFFEINE URINARY METABOLITES
    BUTLER, MA
    LANG, NP
    YOUNG, JF
    CAPORASO, NE
    VINEIS, P
    HAYES, RB
    TEITEL, CH
    MASSENGILL, JP
    LAWSEN, MF
    KADLUBAR, FF
    [J]. PHARMACOGENETICS, 1992, 2 (03): : 116 - 127
  • [8] DEGUCHI T, 1990, J BIOL CHEM, V265, P12757
  • [9] EVANS DAP, 1989, PHARMACOL THERAPEUT, V42, P157
  • [10] IDENTIFICATION OF THE MUTAGENS IN COOKED BEEF
    FELTON, JS
    KNIZE, MG
    SHEN, NH
    ANDRESEN, BD
    BJELDANES, LF
    HATCH, FT
    [J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 1986, 67 : 17 - 24