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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
来源:
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.
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页码:1535 / 1541
页数:7
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