Genetic polymorphisms of estrogen receptor alpha, CYP19, catechol-O-methyltransferase are associated with familial prostate carcinoma risk in a Japanese population

被引:74
作者
Suzuki, K [1 ]
Nakazato, H [1 ]
Matsui, H [1 ]
Koike, H [1 ]
Okugi, H [1 ]
Kashiwagi, B [1 ]
Nishii, M [1 ]
Ohtake, N [1 ]
Nakata, S [1 ]
Ito, K [1 ]
Yamanaka, H [1 ]
机构
[1] Gunma Univ, Sch Med, Dept Urol, Maebashi, Gumma 3718511, Japan
关键词
familial prostate carcinoma; low-penetrance gene; estrogen receptor; alpha; CYP19; catechol-O-methyltransferas; genetic polymorphism;
D O I
10.1002/cncr.11639
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Estrogen is one of the crucial hormones participating in the proliferation and carcinogenesis of the prostate glands. Genetic polymorphisms in the estrogen metabolism pathway might be involved in the risk of prostate carcinoma development. The authors evaluated the association between genetic polymorphisms in estrogen-related enzymes and receptors and the risk of developing familial prostate carcinoma. METHODS. in the current study, 101 cases with prostate carcinoma whose first-degree relatives had prostate carcinoma and 114 healthy age and residence-matched male controls were enrolled. The genotypes of estrogen receptor (ER) alpha, aromatase (CYP19), and catechol-O-methyltransferase (COMT) genes were analyzed. RESULTS. For single polymorphisms, a significant association of the T/T genotype of the PvuII site in the ER alpha gene (odds ratio [OR], 3.44; 95% confidence interval [CI], 1.97-5.99; P = 0.0028), and the C/T and T/T genotypes of the CYP19 gene (OR, 1.77; 95% CI, 1.02-3.09; P = 0.037) with prostate carcinoma risk, was observed. The G/A genotype of the COMT gene showed a weak tendency toward increased risk (OR, 1.48; 95% CI, 0.85-2.57; P = 0.18). Stratification of cases according to clinical stage and pathologic grade showed that the C/T and T/T genotypes of the CYP19 gene were associated significantly with high-grade carcinoma (OR, 2.59; 95% CI, 1.47-4.46; P = 0.048). The number of high-risk genotypes (the T/T in ER alpha, the C/T and T/T in CYP19, and the G/A in COMT) significantly increased the risk of developing prostate carcinoma (2 genotypes: OR, 3.00; 95% CI, 1.72-5.23; P = 0.008; 3 genotypes: OR, 6.30; 95% CI, 3.61-10.99; P = 0.002). CONCLUSIONS. Genetic polymorphisms of genes in the estrogen metabolism pathway were associated significantly with familial prostate carcinoma risk. Single nucleotide polymorphisms of low-penetrance genes are targets for understanding the genetic susceptibility of familial prostate carcinoma. Cancer 2003;98:1411-6. (C) 2003 American Cancer Society.
引用
收藏
页码:1411 / 1416
页数:6
相关论文
共 44 条
[31]   SYNERGISTIC EFFECTS OF ESTROGEN AND ANDROGEN ON THE PROSTATE - EFFECTS OF ESTROGEN ON ANDROGEN-RECEPTORS AND ESTROGEN-RECEPTORS, BRDU UPTAKE, IMMUNOHISTOCHEMICAL STUDY OF AR, AND RESPONSES TO ANTIANDROGENS [J].
SUZUKI, K ;
ITO, K ;
SUZUKI, T ;
HONMA, S ;
YAMANAKA, H .
PROSTATE, 1995, 26 (03) :151-163
[32]  
Suzuki K, 2002, ANTICANCER RES, V22, P3507
[33]  
Suzuki K, 2001, ANTICANCER RES, V21, P3861
[34]   SYNERGISTIC EFFECTS OF ESTROGEN WITH ANDROGEN ON THE PROSTATE - EFFECTS OF ESTROGEN ON THE PROSTATE OF ANDROGEN-ADMINISTERED RATS AND 5-ALPHA-REDUCTASE ACTIVITY [J].
SUZUKI, K ;
TAKEZAWA, Y ;
SUZUKI, T ;
HONMA, S ;
YAMANAKA, H .
PROSTATE, 1994, 25 (04) :169-176
[35]   A candidate prostate cancer susceptibility gene at chromosome 17p [J].
Tavtigian, SV ;
Simard, J ;
Teng, DHF ;
Abtin, V ;
Baumgard, M ;
Beck, A ;
Camp, NJ ;
Carillo, AR ;
Chen, Y ;
Dayananth, P ;
Desrochers, M ;
Dumont, M ;
Farnham, JM ;
Frank, D ;
Frye, C ;
Ghaffari, S ;
Gupte, JS ;
Hu, R ;
Iliev, D ;
Janecki, T ;
Kort, EN ;
Laity, KE ;
Leavitt, A ;
Leblanc, G ;
McArthur-Morrison, J ;
Pederson, A ;
Penn, B ;
Peterson, KT ;
Reid, JE ;
Richards, S ;
Schroeder, M ;
Smith, R ;
Snyder, SC ;
Swedlund, B ;
Swensen, J ;
Thomas, A ;
Tranchant, M ;
Woodland, AM ;
Labrie, F ;
Skolnick, MH ;
Neuhausen, S ;
Rommens, J ;
Cannon-Albright, LA .
NATURE GENETICS, 2001, 27 (02) :172-180
[36]  
Thompson PA, 1998, CANCER RES, V58, P2107
[37]  
Vermeulen A, 2002, Aging Male, V5, P98, DOI 10.1080/713604678
[38]   Arginine-cysteine polymorphism at codon 264 of the human CYP19 gene does not affect aromatase activity [J].
Watanabe, J ;
Harada, N ;
Suemasu, K ;
Higashi, Y ;
Gotoh, O ;
Kawajiri, K .
PHARMACOGENETICS, 1997, 7 (05) :419-424
[39]   Estrogen receptor α gene polymorphisms and endometrial cancer risk [J].
Weiderpass, E ;
Persson, I ;
Melhus, H ;
Wedrén, S ;
Kindmark, A ;
Baron, JA .
CARCINOGENESIS, 2000, 21 (04) :623-627
[40]   Evidence for a prostate cancer susceptibility locus on the X chromosome [J].
Xu, JF ;
Meyers, D ;
Freije, D ;
Isaacs, S ;
Wiley, K ;
Nusskern, D ;
Ewing, C ;
Wilkens, E ;
Bujnovszky, P ;
Bova, GS ;
Walsh, P ;
Isaacs, W ;
Schleutker, J ;
Matikainen, M ;
Tammela, T ;
Visakorpi, T ;
Kallioniemi, OP ;
Berry, R ;
Schaid, D ;
French, A ;
McDonnell, S ;
Schroeder, J ;
Blute, M ;
Thibodeau, S ;
Grönberg, H ;
Emanuelsson, M ;
Damber, JE ;
Bergh, A ;
Jonsson, BA ;
Smith, J ;
Bailey-Wilson, J ;
Carpten, J ;
Stephan, D ;
Gillanders, E ;
Amundson, I ;
Kainu, T ;
Freas-Lutz, D ;
Baffoe-Bonnie, A ;
Van Aucken, A ;
Sood, R ;
Collins, F ;
Brownstein, M ;
Trent, J .
NATURE GENETICS, 1998, 20 (02) :175-179