GSTM1, GSTP1, CYP1A1 and CYP2D6 polymorphisms in lung cancer patients from an environmentally polluted region of Poland:: correlation with lung DNA adduct levels

被引:51
作者
Butkiewicz, D [1 ]
Cole, KJ
Phillips, DH
Harris, CC
Chorazy, M
机构
[1] Ctr Oncol, Dept Tumor Biol, PL-44100 Gliwice, Poland
[2] Haddow Labs, Canc Res Inst, Sect Mol Carcinogenesis, Surrey, England
[3] NCI, Human Carcinogenesis Lab, NIH, Bethesda, MD 20892 USA
关键词
GST and CYP polymorphism; lung cancer; PAH-DNA adduct levels;
D O I
10.1097/00008469-199908000-00008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The CYP and GST genetic polymorphisms, controlling metabolism of xenobiotics, are considered to influence an individual's susceptibility to environmental and occupational carcinogens and predisposition to cancer. In the study, the effect of the GSTM1, GSTP1, CYB1A1 and CYP2D6 polymorphisms was investigated in relation to PAH-DNA adduct levels in non-tumourous lung tissue from non-small cell lung cancer (NSCLC) patients living in the industrialized region of Upper Silesia, Poland. The level of adducts among smokers was significantly elevated when compared to non-smokers (P = 0.0005). Adduct levels correlated inversely with age of patients (P = 0.00001). The GSTP1 and CYP2D6 polymorphisms had no influence on DNA adduct levels. There was a significant relationship between high adduct levels and the combined GSTM1 (null)/CYP1A1-Ile-Val genotype in the squamous cell carcinoma group (P = 0.028). An elevated number of adducts was found in patients with the GSTM1 (null)/CYP1A1-Ile/Val genotype compared to the GSTM1 (null)/CYP1A1-Ile/Ile carriers (P = 0.043). A higher frequency of the CYP1A1-Ile/Val and GSTM1 (null)/CYP1A1-Ile/Val genotypes was observed in patients dth high adduct levels (P = 0.05 and P = 0.009, respectively). A significant prevalence of the GSTM1 (null)/CYP1A1-Ile/Val carriers in the adenocarcinoma group was found (P = 0.003). Thus, our findings imply that the GSTM1 and CYP1A1 exon 7 polymorphisms may influence PAH-DNA adduct levels in target tissue from NSCLC patients, especially in the squamous cell carcinoma group. Moreover, individuals carrying the GSTM1 (null)/CYP1A1-Ile/Val genotype might exhibit a greater predisposition to a peripheral type of lung cancer. (C) 1999 Lippincott Williams & Wilkins.
引用
收藏
页码:315 / 323
页数:9
相关论文
共 44 条
  • [1] ANTTILA S, 1993, CANCER RES, V53, P5643
  • [2] METABOLIC POLYMORPHISM AFFECTING DNA-BINDING AND EXCRETION OF CARCINOGENS IN HUMANS
    BARTSCH, H
    ROJAS, M
    ALEXANDROV, K
    CAMUS, AM
    CASTEGNARO, M
    MALAVEILLE, C
    ANTTILA, S
    HIRVONEN, K
    HUSGAFVELPURSIAINEN, K
    HIETANEN, E
    VAINIO, H
    [J]. PHARMACOGENETICS, 1995, 5 : S84 - S90
  • [3] CARCINOGEN METABOLISM AND DNA ADDUCTS IN HUMAN LUNG TISSUES AS AFFECTED BY TOBACCO SMOKING OR METABOLIC PHENOTYPE - A CASE-CONTROL STUDY ON LUNG-CANCER PATIENTS
    BARTSCH, H
    PETRUZZELLI, S
    DEFLORA, S
    HIETANEN, E
    CAMUS, AM
    CASTEGNARO, M
    GENESTE, O
    CAMOIRANO, A
    SARACCI, R
    GIUNTINI, C
    [J]. MUTATION RESEARCH, 1991, 250 (1-2): : 103 - 114
  • [4] Bouchardy C, 1996, CANCER RES, V56, P251
  • [5] Modulation of DNA adduct levels in human mononuclear white blood cells and granulocytes by CYP1A1, CYP2D6 and GSTM1 genetic polymorphisms
    Butkiewicz, D
    Grzybowska, E
    Hemminki, K
    Ovrebo, S
    Haugen, A
    Motykiewicz, G
    Chorazy, M
    [J]. MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1998, 415 (1-2) : 97 - 108
  • [6] CAPORASO N, 1995, PHARMACOGENETICS, V5, P129
  • [7] Craighead John E., 1995, P455
  • [8] A TOBACCO SMOKE-DERIVED NITROSAMINE, 4-(METHYLNITROSAMINO)-1-(3-PYRIDYL)-1-BUTANONE, IS ACTIVATED BY MULTIPLE HUMAN CYTOCHROME P450S INCLUDING THE POLYMORPHIC HUMAN CYTOCHROME P4502D6
    CRESPI, CL
    PENMAN, BW
    GELBOIN, HV
    GONZALEZ, FJ
    [J]. CARCINOGENESIS, 1991, 12 (07) : 1197 - 1201
  • [9] Dallinga JW, 1998, CANCER EPIDEM BIOMAR, V7, P571
  • [10] SEASONAL-VARIATION OF AROMATIC DNA-ADDUCTS IN HUMAN-LYMPHOCYTES AND GRANULOCYTES
    GRZYBOWSKA, E
    HEMMINKI, K
    SZELIGA, J
    CHORAZY, M
    [J]. CARCINOGENESIS, 1993, 14 (12) : 2523 - 2526