Andersson Patiyan, Varenhorst Eberhard, Söderkvist Peter
Division of Cell biology, Department of Biomedicine and Surgery, Faculty of Health Sciences, Linköping University, SE-581 85 Linköping, Sweden.
Eur J Cancer. 2006 Nov;42(16):2833-7. doi: 10.1016/j.ejca.2006.06.030. Epub 2006 Sep 28.
We study the CAG repeat region in exon 1 of the androgen receptor (AR) and the TaqI polymorphism in exon 9 of the vitamin D receptor (VDR) and the association with prostate cancer. 137 incidentally discovered, histologically verified prostate cancers were analysed for CAG repeat length in AR and genotype at the TaqI site of the VDR. 124 control subjects were analysed to determine the CAG repeat length and TaqI genotype determined for 176 control subjects. An unpaired t-test shows that the mean CAG repeat length was significantly (p<0.001) shorter among cases (20.1 repeats) compared with controls (22.5 repeats). Dividing the prostate cohort and controls into tertiles (< or = 19, 20-22, > or = 23 repeats) shows that short repeats are significantly more common among cases (odds ratio (OR) 4.45, p=0.00003). Genotype frequencies for the TaqI polymorphism reveals no significant differences between cases and controls. We conclude that men with a short CAG repeat in the androgen receptor gene have an increased risk of developing prostate cancer.
我们研究了雄激素受体(AR)外显子1中的CAG重复区域以及维生素D受体(VDR)外显子9中的TaqI多态性及其与前列腺癌的关联。对137例偶然发现且经组织学证实的前列腺癌患者进行了AR中CAG重复长度以及VDR的TaqI位点基因型分析。对124名对照受试者进行分析以确定CAG重复长度,并对176名对照受试者确定了TaqI基因型。非配对t检验显示,与对照组(22.5次重复)相比,病例组(20.1次重复)的平均CAG重复长度显著更短(p<0.001)。将前列腺癌队列和对照组分为三分位数(<或=19、20 - 22、>或=23次重复)显示,短重复在病例组中显著更常见(优势比(OR)4.45,p = 0.00003)。TaqI多态性的基因型频率在病例组和对照组之间未显示出显著差异。我们得出结论,雄激素受体基因中CAG重复短的男性患前列腺癌的风险增加。