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자료유형
학술저널
저자정보
Zhao, Cheng-Xiao (The Key Laboratory of Geriatrics, Beijing Hospital & Beijing Institute of Geriatrics) Liu, Ming (School of Basic Medical Science, Shanxi Medical University) Wang, Jian-Ye (Department of Urology and Beijing Hospital, Chinese Ministry of Health) Xu, Yong (Department of Urology, The Second Hospital of Tianjin Medical University) Wei, Dong (Department of Urology and Beijing Hospital, Chinese Ministry of Health) Yang, Kuo (Department of Urology, The Second Hospital of Tianjin Medical University) Yang, Ze (The Key Laboratory of Geriatrics, Beijing Hospital & Beijing Institute of Geriatrics)
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제14권 제11호
발행연도
2013.1
수록면
6,733 - 6,738 (6page)

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Multiple genetic studies have confirmed association of 8q24 variants with susceptibility to prostate cancer (PCa). As PCa risk SNPs may also influence disease outcome, we studied here eight 8q24 risk alleles, and evaluated their role in PCa clinical covariates in northern Chinese men. Blood samples and clinical information were collected from ethnically Chinese men from Northern China with histologically-confirmed PCa (n=289) and from age-matched normal controls (n=288). Eight 8q24 SNPs were genotyped by polymerase chain reaction-high- resolution melting analysis in 577 subjects. We examined the prevalence distribution of 8q24 risk alleles and analyzed the associations between the risk allele and PCa and clinical covariates to infer their impact on aggressive PCa. Three of the eight SNPs were associated with PCa risk in northern Chinese men, including rs16901966 (OR 1.31, 95% CI 1.01-1.70, p=0.042), rs1447295 (OR 1.47, 95% CI 1.09-1.98, p=0.011) and rs10090154 (OR 1.55, 95% CI 1.14-2.12, p=0.005). Haplotype analysis based association with the risk alleles revealed significant differences between cases and controls (OR 1.43, 95%CI 0.99-2.06, p=0.049). The risk alleles rs16901966, rs1447295 and rs10090154 were associated with age at diagnosis and tumor stage as compared with controls, while rs16901966 was associated with aggressive PCa (OR 1.43, 95% CI 1.01-2.03, p=0.042). The evidence for 8q24 SNPs with PCa risk in northern Chinese men showed rs16901966, rs1447295 and rs10090154 at 8q24 (region 1, region 2) to be strongly associated with PCa and clinical covariates. The three SNPs at 8q24 could be PCa susceptible genetic markers in northern Chinese men.

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