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Cancer Research 66, 11077, November 15, 2006. doi: 10.1158/0008-5472.CAN-06-3024
© 2006 American Association for Cancer Research

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Epidemiology and Prevention

Germ-Line Genetic Variation in the Key Androgen-Regulating Genes Androgen Receptor, Cytochrome P450, and Steroid-5-{alpha}-Reductase Type 2 Is Important for Prostate Cancer Development

Sara Lindström1, Fredrik Wiklund2, Hans-Olov Adami2, Katarina Augustsson Bälter2, Jan Adolfsson3 and Henrik Grönberg2

1 Department of Radiation Sciences, Oncology, Umeå University, Umeå, Sweden and 2 Department of Medical Epidemiology and Biostatistics and 3 Oncologic Center, CLINTEC, Karolinska Institutet, Stockholm, Sweden

Requests for reprints: Sara Lindström, Department of Radiation Sciences, Oncology, Umeå University, SE-901 85 Umeå, Sweden. Phone: 46-90-785-47-34; Fax: 46-90-12-74-64; E-mail: sara.lindstrom{at}oc.umu.se.

Prostate cancer risk may be influenced by single genetic variants in the hormone-regulating genes androgen receptor (AR), cytochrome P450 (CYP17), and steroid-5-{alpha}-reductase type 2 (SRD5A2). In this study, we comprehensively investigated polymorphisms in these three loci and their joint effect in a large population-based study. We selected 23 haplotype-tagging single-nucleotide polymorphisms (htSNP) that could uniquely describe >95% of the haplotypes (6 in AR, 6 in CYP17, and 11 in SRD5A2). These htSNPs were then genotyped in the Cancer Prostate in Sweden population (2,826 case subjects and 1,705 controls). We observed significant association for several SNPs in the AR gene (P = 0.004-0.02) and CYP17 (P = 0.009-0.05) and one SNP in SRD5A2 (P = 0.02). Carriers of the most common AR haplotype had a significant excess risk to develop prostate cancer [odds ratio (OR), 1.25; 95% confidence interval (95% CI), 1.1-1.5; P = 0.002], yielding an estimated population attributable risk of 16% (95% CI, 0.06-0.25). Combining risk alleles from these genes yielded a 12% risk increase for each additional high-risk allele carried (95% CI, 1.1-1.2; P for trend = 9.2 x 10–5), with an overall OR of 1.87 (95% CI, 1.0-3.4) for carriers of all five included risk alleles, an OR of 2.13 (P for trend = 8 x 10–4) for advanced disease, and an OR of 4.35 (P for trend = 7 x 10–5) for disease onset before age 65 years. Genetic variation in key genes in the androgen pathway is important for development of prostate cancer and may account for a considerable proportion of all prostate cancers. Carriers of five high-risk alleles in the AR, CYP17, and SRD5A2 genes are at ~2-fold excess risk to develop prostate cancer. (Cancer Res 2006; 66(22): 11077-83)




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2006 by the American Association for Cancer Research.