Positive correlation between single or combined genotypes of CYP1A1 and GSTM1 in relation to prostate cancer in Chilean people

被引:60
作者
Acevedo, C
Opazo, JL
Huidobro, C
Cabezas, J
Iturrieta, J
Sepúlveda, LQ
机构
[1] Univ Chile, Fac Med, ICBM, Program Mol & Clin Pharmacol,Lab Chem Carcinogene, Santiago 7, Chile
[2] Corp Nacl Canc, Santiago, Chile
关键词
CYP1A1; Msp1; GSTM1; polymorphisms; prostate cancer;
D O I
10.1002/pros.10274
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND. The prostate cancer is a slowly progressing disease that begins decades prior to diagnosis. It has been suggested that there might be differences in susceptibility due to genetic polymorphisms in biotransformation enzyme genes. In the present work, associations between CYP1A1(Msp1), GSTM1(-/-) polymorphisms, and prostate cancer were analyzed in a case-control study. METHODS. Genomic DNA was isolated from peripheral blood samples, collected on EDTA. PCR-RFLP was used to determine simultaneously Msp1 and GSTM1 (-/-) polymorphisms. RESULTS. In cancer patients, frequency of m2 variant allele (0.377) and GSTM1(-/-) (0.362) showed statistically significant increases compared to the control group (0.262 and 0.227, respectively). The estimate relative risks (OR) were higher for individuals carrying combined CYP1A1 and GSTM1 rare genotypes, in relation to individuals carrying CYP1A1 or GSTM1 alone. Multivariate logistic regression analysis including confounding factors (age, digital examination, and PSA antigen) showed even higher risk for individuals carrying m2m2 genotype (OR = 3.99; 95% CI, 1.27-12.54), GST(-/-) genotype (OR = 2.75; 95% CI, 1.31-5.79), and m2m2/GST(-) genotype (OR = 16.63; 95% CI, 1.67-165.48). CONCLUSIONS. Taken together, these findings suggest that Chilean people carrying single or combined GSTM1 and CYP1A1 polymorphisms are more susceptible to prostate cancer. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:111 / 117
页数:7
相关论文
共 37 条
  • [1] GENETIC SUSCEPTIBILITY TO LUNG-CANCER WITH SPECIAL EMPHASIS ON CYP1A1 AND GSTM1 - A STUDY ON HOST FACTORS IN RELATION TO AGE AT ONSET, GENDER AND HISTOLOGICAL CANCER TYPES
    ALEXANDRIE, AK
    SUNDBERG, MI
    SEIDEGARD, J
    TORNLING, G
    RANNUG, A
    [J]. CARCINOGENESIS, 1994, 15 (09) : 1785 - 1790
  • [2] AMBROSONE CB, 1995, CANCER RES, V55, P3483
  • [3] Aynacioglu AS, 1998, ARCH TOXICOL, V72, P215
  • [4] GENETIC RISK AND CARCINOGEN EXPOSURE - A COMMON INHERITED DEFECT OF THE CARCINOGEN-METABOLISM GENE GLUTATHIONE-S-TRANSFERASE M1 (GSTM1) THAT INCREASES SUSCEPTIBILITY TO BLADDER-CANCER
    BELL, DA
    TAYLOR, JA
    PAULSON, DF
    ROBERTSON, CN
    MOHLER, JL
    LUCIER, GW
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (14) : 1159 - 1164
  • [5] Cascorbi I, 1996, CANCER RES, V56, P4965
  • [6] Coughlin SS, 1996, AM J EPIDEMIOL, V143, P1002, DOI 10.1093/oxfordjournals.aje.a008663
  • [7] A WORSE PROGNOSIS FOR SMOKERS WITH PROSTATE-CANCER
    DANIELL, HW
    [J]. JOURNAL OF UROLOGY, 1995, 154 (01) : 153 - 157
  • [8] Giovannucci E, 1999, CANCER EPIDEM BIOMAR, V8, P277
  • [9] The CAG repeat within the androgen receptor gene and its relationship to prostate cancer
    Giovannucci, E
    Stampfer, MJ
    Krithivas, K
    Brown, M
    Brufsky, A
    Talcott, J
    Hennekens, CH
    Kantoff, PW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (07) : 3320 - 3323
  • [10] Cancer statistics, 2000
    Greenlee, RT
    Murray, T
    Bolden, S
    Wingo, PA
    [J]. CA-A CANCER JOURNAL FOR CLINICIANS, 2000, 50 (01) : 7 - 33