Association study of polymorphisms in the human estrogen ReceptorAlpha gene and prostate cancer risk

被引:23
作者
Cancel-Tassin, G
Latil, A
Rousseau, F
Mangin, P
Bottius, E
Escary, JL
Berthon, P
Cussenot, O
机构
[1] UroGene, F-91058 Evry, France
[2] GenOdyssee, F-91974 Courtaboeuf, France
[3] Fac Med, CeRePP EA3104, F-75270 Paris, France
[4] Ctr Hosp Univ Nancy Brabois, Serv Urol, F-54500 Vandoeuvre Les Nancy, France
[5] Hop St Louis, Urol Serv, F-75010 Paris, France
[6] Inst Univ France, F-75005 Paris, France
关键词
prostate cancer; estrogen receptor alpha gene; polymorphism;
D O I
10.1016/S0302-2838(03)00319-1
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Prostate cancer is a very common hormone-related malignancy in Western countries. It is initially dependent on androgen stimulation but in vitro growth of prostate cancer cells are also dependent on estrogen. Our goal was to elucidate if some polymorphisms of estrogen receptor alpha gene might be associated with the risk of prostate cancer. Methods: Using DHPLC techniques, each coding exon of the estrogen receptor alpha gene was screened for new polymorphisms in germline DNA from 96 healthy controls and 96 sporadic prostate cancer cases. Identified polymorphisms were then genotyped and their distribution compared between the two populations. Results: Thirteen polymorphisms were identified. A difference was found in the distribution of one newly identified polymorphism, namely a GGGA repeat located in the first intron of the gene. The common wild type genotype consisted of two alleles with five GGGA repetitions (515 genotype). Indeed this 5/5 genotype was found in 294/296 controls (99.3%) and 285/294 patients (96.9%; OR, 4.6; 95% CI, 0.99-21.67). Among the nine patients with a different genotype, one was 4/5, seven were 5/6 and one was 6/6. Conclusion: These results suggest that variants of the GGGA polymorphism from the estrogen receptor alpha gene may be associated with an increased risk of developing prostate cancer. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:487 / 490
页数:4
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