Mittal Rama D, Manchanda Parmeet K, Bhat Sanjay, Bid Hemant K
Sanjay Gandhi PGIMS, Urology and Renal Transplantation, Lucknow, Uttar Pradesh, India.
BJU Int. 2007 Apr;99(4):933-7. doi: 10.1111/j.1464-410X.2007.06657.x.
To explore the association of vitamin-D receptor (VDR) genotypes and haplotypes (variants at the Fok-I, and Taq-I sites) with the risk of bladder cancer, as vitamin D is antiproliferative and reported to induce apoptosis in human bladder tumour cells in vitro.
PATIENTS, SUBJECTS AND METHODS: A case-control study using polymerase chain reaction-restriction fragment length polymorphism was conducted in 130 patients with bladder cancer and 346 normal healthy individuals in a north Indian population. Patients were also categorized according to grade and stage of tumour.
There was a significant difference in genotype and allelic distribution of VDR (Fok-I) polymorphism in the patients (P = 0.033 and = 0.017, respectively). The FF genotype was associated with twice the risk for bladder cancer (odds ratio 2.042, 95% confidence interval, CI, 0.803-5.193). There was no significant difference in genotypic distribution or allelic frequencies of the VDR (Taq-I) polymorphism (P = 0.477 and 0.230) when compared with the controls. The stage and grade of the bladder tumours had no association with VDR (Fok-I and Taq-I) genotypes. There was a significant difference in the frequency distribution of the haplotypes FT and fT (P < 0.001); these haplotypes had a protective effect in the control group (odds ratio 0.167, 95% CI 0.096-0.291, and 0.079, 0.038-0.164).
These data suggest that VDR (Fok-I) polymorphism is associated with the risk of bladder cancer. Further, the results for the haplotype FT and fT indicate that patients with this haplotype have a lower risk of developing bladder cancer than those with other haplotypes.
探讨维生素D受体(VDR)基因多态性及单倍型(Fok-I和Taq-I位点的变异)与膀胱癌风险的关联,因为维生素D具有抗增殖作用,且据报道在体外可诱导人膀胱肿瘤细胞凋亡。
患者、研究对象与方法:在印度北部人群中,对130例膀胱癌患者和346名正常健康个体进行了一项采用聚合酶链反应-限制性片段长度多态性的病例对照研究。患者还根据肿瘤的分级和分期进行了分类。
患者中VDR(Fok-I)多态性的基因型和等位基因分布存在显著差异(P值分别为0.033和0.017)。FF基因型与膀胱癌风险增加两倍相关(优势比2.042,95%置信区间,CI,0.803 - 5.193)。与对照组相比,VDR(Taq-I)多态性的基因型分布或等位基因频率无显著差异(P值分别为0.477和0.230)。膀胱肿瘤的分期和分级与VDR(Fok-I和Taq-I)基因型无关联。单倍型FT和fT的频率分布存在显著差异(P < 0.001);这些单倍型在对照组中具有保护作用(优势比0.167,95% CI 0.096 - 0.291,以及0.079,0.038 - 0.164)。
这些数据表明VDR(Fok-I)多态性与膀胱癌风险相关。此外,单倍型FT和fT的结果表明,具有该单倍型的患者患膀胱癌的风险低于具有其他单倍型的患者。