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Clinical Cancer Research 13, 5959, October 1, 2007. doi: 10.1158/1078-0432.CCR-07-0702
© 2007 American Association for Cancer Research

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Cancer Susceptibility and Prevention

Association of RNASEL Variants with Prostate Cancer Risk in Hispanic Caucasians and African Americans

Stacie J. Shook1, Joke Beuten1, Kathleen C. Torkko5, Teresa L. Johnson-Pais2, Dean A. Troyer3, Ian M. Thompson4 and Robin J. Leach1,2,4

Authors' Affiliations: Departments of 1 Cellular and Structural Biology, 2 Pediatrics, 3 Pathology, and 4 Urology, The University of Texas Health Science Center, San Antonio, Texas and 5 Departments of Pathology and Preventive Medicine and Biometrics, University of Colorado at Denver and Health Sciences Center, Aurora, Colorado

Requests for reprints: Robin J. Leach, Department of Cellular and Structural Biology, University of Texas Health Science Center, 7703 Floyd Curl Drive, San Antonio, TX 78229-3900. Phone: 210-567-6947; Fax: 210-567-6781; E-mail: leach{at}uthscsa.edu.

Purpose: The RNASEL gene at 1q25 has been identified as a hereditary prostate cancer susceptibility gene, but to date, no study has investigated the role of RNASEL variants in Hispanic Caucasian men with prostate cancer.

Experimental Design: Two RNASEL common variants, located at amino acids 462 and 541, were genotyped in non-Hispanic Caucasian, Hispanic Caucasian, and African American prostate cancer cases and controls.

Results: The RNASEL 462 AA genotype was found to increase prostate cancer risk over 4-fold in Hispanic Caucasians [odds ratio (OR), 4.43; 95% confidence interval (95% CI), 1.68-11.68; P = 0.003] and over 10-fold in African Americans (OR, 10.41; 95% CI, 2.62-41.40; P = 0.001) when compared with the GG genotype. Analysis of the RNASEL 541 variant showed that Hispanic Caucasian patients with the GG genotype had a statistically significant increase in their risk for developing prostate cancer when compared with the TT and GT genotypes (OR, 1.91; 95% CI, 1.16-3.14; P = 0.01). A common G-T haplotype for the combination of the RNASEL 462 and 541 variants was found to occur more frequently in controls compared with cases in African Americans (P = 0.04) but not in non-Hispanic Caucasians or Hispanic Caucasians.

Conclusions: This is the first study that investigates the association of prostate cancer risk with RNASEL variants in Hispanic men. Our data support the role of RNASEL as a predisposition gene for prostate cancer and showed a significant association between the RNASEL 462 variant and prostate cancer risk in African Americans and Hispanic Caucasians.




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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 © 2007 by the American Association for Cancer Research.