Combination of polymorphisms from genes related to estrogen metabolism and risk of prostate cancers: The hidden face of estrogens

被引:81
作者
Cussenot, Olivier
Azzouzi, Abdel Rhamene
Nicolaiew, Nathalie
Fromont, Gaelle
Mangin, Philippe
Cormier, Luc
Fournier, Georges
Valeri, Antoine
Larre, Stephane
Thibault, Frederic
Giordanella, Jean-Pierre
Pouchard, Michel
Zheng, Yan
Hamdy, Freddie C.
Cox, Angela
Cancel-Tassin, Geraldine
机构
[1] Hop Tenon, Serv Urol, F-75020 Paris, France
[2] Ctr Rech Pathol Prostatique, Paris, France
[3] Univ Paris 06, Assistance Publ Hop Paris, Ctr Rech Pathol Prostatiques, Grp Hosp Univ Est, Paris, France
[4] Univ Paris 12, Fac Med, Inst Natl Sante & Rech Med, EMI0337 IFR10, Creteil, France
[5] CHU Angers, Dept Urol, Angers, France
[6] Univ Poitiers, CHU La Miletrie, Dept Pathol, Poitiers, France
[7] CHU Brabois, Dept Urol, Nancy, France
[8] Hop Cavale Blanche, Dept Urol, Brest, France
[9] Hop Cavale Blanche, Dept Breast, Brest, France
[10] Univ Sheffield, Royal Hallamshire Hosp, Acad Urol Unit, France Inst Canc Studies Caisse Natl Assurance M, Sheffield S10 2JF, S Yorkshire, England
关键词
D O I
10.1200/JCO.2007.11.0908
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose The association between common functional polymorphisms from the CYP17, CYP19, CYP1B1, and COMT genes involved in the estrogen metabolism and the risk of prostate carcinoma was evaluated. Patients and Methods The study investigated 1,983 white French men ( 1,101 patients with prostate cancer and 882 healthy controls) aged between 40 and 98 years. The different alleles and genotypes were analyzed according to case-control status, aggressiveness pattern of the tumors, age at onset, and family history of cancers. Results The VV ( high activity) genotype of the V432L polymorphism from CYP1B1 ( odds ratio [ OR] = 1.36; 95% CI, 1.03 to 1.79; P = .031), and the long allele ( > 175 bp) of the TTTA repeat from CYP19 ( OR, 1.26; 95% CI, 1.08 to 1.47; P = .003) were significantly associated with the risk of prostate cancer. An additive effect was observed when we combined the two at-risk alleles ( OR = 1.63; 95% CI, 1.24 to 2.13; P < .001). The association was stronger for the CYP1B1 VV genotype ( OR = 1.55; 95% CI, 1.13 to 2.13; P = .007) among the group of patients with highly aggressive disease. Stratification by age at onset showed that the associations of CYP1B1 and CYP19 variants were largely confined to the younger prostate cancer patients. Conclusion This association between polymorphisms from genes related to estrogen metabolism and prostate cancer risk suggest new clinical considerations in the management of prostate cancer: the development of new prevention trials based on genetic profiling and the evaluation of specific inhibitors involving the estrogen pathways.
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页码:3596 / 3602
页数:7
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