Vitamin D receptor polymorphisms as markers in prostate cancer

被引:91
作者
Correa-Cerro, L
Berthon, P
Häussler, J
Bochum, S
Drelon, E
Mangin, P
Fournier, G
Paiss, T
Cussenot, O
Vogel, W
机构
[1] Univ Ulm, Dept Med Genet, D-89069 Ulm, Germany
[2] Univ Guadalajara, Guadalajara, Jalisco, Mexico
[3] Univ Paris 07, Hop St Louis, Paris, France
[4] CHU Cavale Blanche, Serv Urol, Brest, France
[5] Univ Ulm, Dept Urol, D-89069 Ulm, Germany
关键词
D O I
10.1007/s004390051102
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Polymorphisms in the vitamin D receptor (VDR) gene have been analyzed in several studies for an association with prostate cancer (PCA) and odds ratios (OR) greater than or equal to 3 have been observed in study populations from North America. We studied three polymorphisms in the VDR gene (poly-A microsatellite, TaqI and FokI RFLPs) in 105 controls and 132 sporadic PCA cases fi:om France and in a collection of families from Germany and France. The polymorphisms near the 3' end of the gene were in linkage disequilibrium with an almost complete coincidence of the short poly-A alleles and t (presence of the restriction site) of the TaqI polymorphism, (contingency tables, P<0.0001). An association was found by logistic regression for the poly-A between PCA and the heterozygous genotype (S/L; S<17, L greater than or equal to 17, OR=0.44, 95% confidence interval, CI=0.198-0.966, P=0.041). OR. was lower in patients less than or equal to 70 years old and patients with a Gleason score greater than or equal to 6. The Tt genotype of the TaqI RFLP also showed an association with PCA (OR=0.5, CI0.27-0.92, P=0.026). This association was also stronger for patients less than or equal to 70 years old (OR=0.31, CI=0.15-0.63, P=0.001). The risk alleles were S and t alleles as indicated by the OR of the homozygotes, although these were not significant. The FokI RFLP at the 5' end of the gene did not reveal any association (P>0.7). While some association studies differ between Europe and North America, our present findings with the VDR gene agree with those from North America, indicating a weak but general role of the VDR in PCA susceptibility.
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页码:281 / 287
页数:7
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