Variants of N-acetyltransferase NAT1 and a case-control study of colorectal adenomas

被引:70
作者
Lin, HJ
Probst-Hensch, NM
Hughes, NC
Sakamoto, GT
Louie, AD
Kau, IH
Lin, BK
Lee, DB
Lin, J
Frankl, HD
Lee, ER
Hardy, S
Grant, DM
Haile, RW
机构
[1] Harbor UCLA Med Ctr, Div Med Genet, Torrance, CA 90509 USA
[2] Harbor UCLA Med Ctr, Div Gastroenterol, Torrance, CA 90509 USA
[3] Univ So Calif, Kenneth Norris Jr Comprehens Canc Ctr, Los Angeles, CA 90033 USA
[4] Univ So Calif, Dept Prevent Med, Los Angeles, CA 90089 USA
[5] Kaiser Permanente Med Ctr, Div Gastroenterol, Los Angeles, CA 90034 USA
[6] Kaiser Permanente Med Ctr, Div Gastroenterol, Bellflower, CA USA
[7] Hosp Sick Children, Res Inst, Div Clin Pharmacol & Toxicol, Toronto, ON M5G 1X8, Canada
[8] Univ Calif Los Angeles, Sch Med, Dept Surg, Tissue Typing Lab, Los Angeles, CA 90024 USA
来源
PHARMACOGENETICS | 1998年 / 8卷 / 03期
关键词
colorectal adenomas; heterocyclic amines; N-acetyltransferase; NAT1;
D O I
10.1097/00008571-199806000-00009
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
N-acetyltransferase NAT1, together with enzymes CYP1A2 and NAT2, helps convert heterocyclic amines to mutagens, Epidemiologic studies of the association of variants of these enzymes with colorectal cancer may provide indirect support for a heterocyclic amine mechanism. We used single strand conformation polymorphism and heteroduplex analysis to screen for mutations in the NAT1 coding region in a case-control study (n = 932) of colorectal adenomas, which are precursors to cancer, Thirteen different single-base mutations Were found: (CT)-T-97, (CT)-T-190, (TC)-C-402, G(445)A-G(459)A-T(640)G (a combination of three mutations), (CT)-T-559, G(560)A, A(613)G, A(752)T, (TC)-C-777, G(781)A, and A(787)G. Function of novel mutations was tested by bacterial production of enzymes and measurement of K-m, V-max, and stability However, only 24 control individuals and 18 cases carried an inactivating NAT1 mutation. When combined with our data on the NAT2 acetylation polymorphism, we saw no evidence for an association between N-acetyltransferases and prevalence of adenomas, Larger sample sizes are required for further evaluation. Pharmacogenetics 8:269-281 (C) 1998 Lippincott-Raven Publishers.
引用
收藏
页码:269 / 281
页数:13
相关论文
共 49 条
[1]  
BELL DA, 1995, CANCER RES, V55, P3537
[2]  
BELL DA, 1995, CANCER RES, V55, P5226
[3]   Does increased endogenous formation of N-nitroso compounds in the human colon explain the association between red meat and colon cancer? [J].
Bingham, SA ;
Pignatelli, B ;
Pollock, JRA ;
Ellul, A ;
Malaveille, C ;
Gross, G ;
Runswick, S ;
Cummings, JH ;
ONeill, IK .
CARCINOGENESIS, 1996, 17 (03) :515-523
[4]  
BIRD CL, 1995, CANCER EPIDEM BIOMAR, V4, P709
[5]  
Bird CL, 1996, AM J EPIDEMIOL, V144, P34, DOI 10.1093/oxfordjournals.aje.a008852
[6]   HUMAN ARYLAMINE N-ACETYLTRANSFERASE GENES - ISOLATION, CHROMOSOMAL LOCALIZATION, AND FUNCTIONAL EXPRESSION [J].
BLUM, M ;
GRANT, DM ;
MCBRIDE, W ;
HEIM, M ;
MEYER, UA .
DNA AND CELL BIOLOGY, 1990, 9 (03) :193-203
[7]  
BOOBIS AR, 1994, CANCER RES, V54, P89
[8]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[9]   COLORECTAL-CANCER - EVIDENCE FOR DISTINCT GENETIC CATEGORIES BASED ON PROXIMAL OR DISTAL TUMOR LOCATION [J].
BUFILL, JA .
ANNALS OF INTERNAL MEDICINE, 1990, 113 (10) :779-788
[10]   Functional polymorphism of the human arylamine N-acetyltransferase type 1 gene caused by C190T and G560A mutations [J].
Butcher, NJ ;
Ilett, KF ;
Minchin, RF .
PHARMACOGENETICS, 1998, 8 (01) :67-72