Title
Prostate Cancer Risk And Esr1 Ta, Esr2 Ca Repeat Polymorphisms
Abstract
Background: Experimental evidence has suggested that estrogen receptor α (coded by the gene ESR1) might increase prostate cancer risk, whereas estrogen receptor B (coded by the gene ESR2) might reduce prostate cancer risk. Methods: We investigated the relationship with prostate cancer risk of both a TA repeat polymorphism in the ESR1 5′ region, ESR1 (TA)n, and with a CA repeat polymorphism in intron 5 of ESR2, ESR2 (CA)n, in a case-control study (545 cases and 674 controls) nested in the Physicians' Health Study. Results: Prostate cancer risk was highest for carriers of ESR1 (TA) 24 and ESR1 (TA)25. Replacing one modal ESR1 (TA) 14 allele with one ESR1 (TA)24 allele yielded an odds ratio of 1.42 (95% confidence interval, 1.00-2.00; P = 0.05). Replacing one ESR1 (TA)14 allele with one ESR1 (TA)25 allele yielded an odds ratio of 2.10 (95% confidence interval, 1.15-3.84; P = 0.02). ESR2 (CA) n showed no effects on prostate cancer risk. Conclusions: The ESR1 (TA)n polymorphism might play a role in prostate cancer risk. Copyright © 2007 American Association for Cancer Research.
Publication Date
11-1-2007
Publication Title
Cancer Epidemiology Biomarkers and Prevention
Volume
16
Issue
11
Number of Pages
2233-2236
Document Type
Article
Personal Identifier
scopus
DOI Link
https://doi.org/10.1158/1055-9965.EPI-07-0481
Copyright Status
Unknown
Socpus ID
38849178040 (Scopus)
Source API URL
https://api.elsevier.com/content/abstract/scopus_id/38849178040
STARS Citation
McIntyre, Matthew H.; Kantoff, Philip W.; Stampfer, Meir J.; Mucci, Lorelei A.; and Parslow, Diane, "Prostate Cancer Risk And Esr1 Ta, Esr2 Ca Repeat Polymorphisms" (2007). Scopus Export 2000s. 5890.
https://stars.library.ucf.edu/scopus2000/5890