Polymorphisms in the glutathione S-transferase M1, T1, and P1 genes and prostate cancer prognosis

被引:27
作者
Agalliu, Ilir
Lin, Daniel W.
Salinas, Claudia A.
Feng, Ziding
Stanford, Janet L.
机构
[1] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98109 USA
[2] Univ Washington, Dept Urol, Seattle, WA 98195 USA
[3] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
关键词
genetic polymorphisms; gluthatione S-transferase; prostate cancer progression; prostate cancer mortality; biomarker;
D O I
10.1002/pros.20491
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND. Polymorphisms in glutathione S-transferase (GST) genes can increase oxidative stress, which may affect cancer prognosis. The aim of this study was to examine associations between GSTM(1), T-1, or P-1 genetic variants and prostate cancer outcomes. METHODS. A population-based cohort of men (n = 752) from King County, Washington, diagnosed with prostate cancer in 1993-1996, and under long-term surveillance for mortality completed a follow-up survey about prostate cancer recurrence/progression. Cox PH models were used to estimate hazard ratios (HR) and 95% confidence intervals (CI) for deaths from prostate cancer or other causes and prostate cancer recurrence/progression. RESULTS. There were 50 prostate cancer-specific deaths, 65 deaths from other causes, and 143 recurrence/progressions events during an average 9.6 years of follow-up. The adjusted HR for prostate cancer mortality was 3.8 (95% CI 1.6-8.9) among Caucasian men with the GSTM(1)-null genotype. There were no differences, however, in mortality from other causes or prostate cancer recurrence/progression between men with GSTM(1)-null versus not-null genotypes. The GSTT, and GSTP(1) genotypes were not associated with any of these outcomes. DISCUSSION. Results suggest that the GSTM(1) genotype maybe a useful biomarker to identify patients at higher risk for fatal prostate cancer.
引用
收藏
页码:1535 / 1541
页数:7
相关论文
共 21 条
  • [1] [Anonymous], 1989, Molecular Cloning: A Laboratory Manual
  • [2] [Anonymous], 1999, APPL SURVIVAL ANAL T
  • [3] COX DR, 1972, J R STAT SOC B, V34, P187
  • [4] GLUTATHIONE TRANSFERASE ISOENZYMES FROM HUMAN PROSTATE
    DIILIO, C
    ACETO, A
    BUCCIARELLI, T
    ANGELUCCI, S
    FELACO, M
    GRILLI, A
    FEDERICI, G
    [J]. BIOCHEMICAL JOURNAL, 1990, 271 (02) : 481 - 485
  • [5] Smoking influences aberrant CpG hypermethylation of multiple genes in human prostate carcinoma
    Enokida, H
    Shiina, H
    Urakami, S
    Terashima, M
    Ogishima, T
    Li, LC
    Kawahara, M
    Nakagawa, M
    Kane, CJ
    Carroll, PR
    Igawa, M
    Dahiya, R
    [J]. CANCER, 2006, 106 (01) : 79 - 86
  • [6] Racial differences in survival among men with prostate cancer and comorbidity at time of diagnosis
    Freeman, VL
    Durazo-Arvizu, R
    Keys, LC
    Johnson, MP
    Schafernak, K
    Patel, VK
    [J]. AMERICAN JOURNAL OF PUBLIC HEALTH, 2004, 94 (05) : 803 - 808
  • [7] Garte S, 2001, CANCER EPIDEM BIOMAR, V10, P1239
  • [8] Racial differences in mortality among Medicare recipients after treatment for localized prostate cancer
    Godley, PA
    Schenck, AP
    Amamoo, MA
    Schoenbach, VJ
    Peacock, S
    Manning, M
    Symons, M
    Talcott, JA
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (22): : 1702 - 1710
  • [9] Glutathione transferases
    Hayes, JD
    Flanagan, JU
    Jowsey, IR
    [J]. ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2005, 45 : 51 - 88
  • [10] The glutathione S-Transferase supergene family: Regulation of GST and the contribution of the isoenzymes to cancer chemoprotection and drug resistance
    Hayes, JD
    Pulford, DJ
    [J]. CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 30 (06) : 445 - 600