Genetic variants in the CYP24A1 gene are associated with prostate cancer risk and aggressiveness in a Korean study population

被引:16
|
作者
Oh, J. J. [1 ,2 ]
Byun, S-S [3 ]
Lee, S. E. [3 ]
Hong, S. K. [3 ]
Jeong, C. W. [3 ]
Choi, W. S. [4 ]
Kim, D. [5 ]
Kim, H. J. [6 ,7 ]
Myung, S. C. [6 ,7 ,8 ]
机构
[1] CHA Univ, Dept Urol, CHA Bundang Med Ctr, Songnam, South Korea
[2] CHA Univ, CHA Canc Res Ctr, Seoul, South Korea
[3] Seoul Natl Univ, Bundang Hosp, Dept Urol, Songnam 463707, Kyunggi Do, South Korea
[4] Choi Won Suk Urol Clin, Yongin, South Korea
[5] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
[6] Chung Ang Univ, Coll Med, Adv Urogenital Dis Res Ctr, Seoul 156756, South Korea
[7] Chung Ang Univ, Coll Med, Res Inst Translat Syst Biom, Seoul 156756, South Korea
[8] Chung Ang Univ, Coll Med, Dept Urol, Seoul 156756, South Korea
基金
新加坡国家研究基金会;
关键词
prostate; CYP24A1; polymorphism; cancer risk; VITAMIN-D-RECEPTOR; SINGLE-NUCLEOTIDE POLYMORPHISMS; D PATHWAY; DISEQUILIBRIUM; DIAGNOSIS; ANDROGEN; VDR;
D O I
10.1038/pcan.2014.1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Vitamin D-deactivating enzyme CYP24A1 had controversial effects on prostate cancer risk; the genetic study also showed the controversial results. Therefore, we identified the relationships between polymorphisms in CYP24A1 and prostate cancer in a Korean cohort. METHODS: We evaluated the association between 21 single-nucleotide polymorphisrns (SNPs) in the CYP24A1 and prostate cancer in Korean men (272 prostate cancers and 173 controls). BPH patients with high PSA or abnormal digital rectal examination who underwent negative prostate biopsy were enrolled in the control group. Twenty-one SNPs in the CYP24A1 were selected from the International HapMap database and the NCBI database with calculation of minor allele frequency and linkage disequilibrium, preferably including the SNPs that were nonsynonymous and located within exons. We also investigated the association between 21 SNPs in the CYP24A1 gene and known clinical characteristics, such as the PSA level, clinical stage, pathological stage and Gleason score. RESULTS: The statistical analysis suggested that five CYP24A1 sequence variants (rs2248461- odds ratio (OR): 0.63, rs2248359-OR: 0.65, rs6022999-OR: 0.65, rs2585428-OR: 0.46, rs4809959 -OR: 0.52) had a significant association with prostate cancer risk after multiple comparisons by a method of false discovery rate. Logistic analyses of the CYP24A1 polymorphisms with several prostate cancer-related factors showed that several SNPs were significant: four SNPs to PSA level, three to clinical stage, two to pathological stage and two SNPs to the Gleason score. CONCLUSIONS: The results of this study suggest that some CYP24A1 gene polymorphisms might be associated with the risk of prostate cancer in Korean men. Five CYP24A1 sequence variants showed the significance to predict prostate cancer, and several SNPs of CYP24A1 gene had an important finding to predict prostate cancer-related factors. However, these results should be validated in future large-scale studies.
引用
收藏
页码:149 / 156
页数:8
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