Urology Service, Department of Surgery, Walter Reed Army Medical Center, Washington, District of Columbia, USA.
Cancer Epidemiol Biomarkers Prev. 2010 Jan;19(1):1-8. doi: 10.1158/1055-9965.EPI-08-1111.
A region on chromosome 8q24 was recently identified as a novel prostate cancer risk locus. Inherited variation in this region is associated with prostate cancer risk in the general population (21-58%), and specific alleles show a strong association in African-American men. This study was designed to evaluate associations between 8q24 risk alleles and clinical variables, such as pathologic stage, age at diagnosis, and recurrence, in a case series of African-American men.
Peripheral blood DNA samples from 114 African-American men with prostate cancer, including 106 who had undergone radical prostatectomy, were genotyped for six single-nucleotide polymorphisms on three 8q24 regions. The presence of these single-nucleotide polymorphisms was compared with clinicopathologic and follow-up data after radical prostatectomy.
The mean age of diagnosis and follow-up time were 57.4 (+/-8.9) years and 49.1 (+/-31.6) months, respectively. Patients carrying the Broad11934905 A risk allele, which is specific for African ancestry, were more likely to have a higher pathologic stage (pT(3-4)) than individuals with the wild type (odds ratio, 4.48; 95% confidence interval, 1.42-14.14; P = 0.011). A trend toward increased frequency of and shorter time to biochemical recurrence was noted in patients with this risk allele on Kaplan-Meier unadjusted survival analysis (P = 0.076).
The Broad11934905 polymorphism at 8q24, which is only found in people of African ancestry, is associated with an increase in non-organ-confined prostate cancer at prostatectomy. In addition, for those with this risk allele, there is a trend toward early biochemical recurrence that requires validation in larger studies.
染色体 8q24 上的一个区域最近被确定为前列腺癌的一个新的风险位点。该区域的遗传变异与普通人群(21-58%)的前列腺癌风险相关,特定等位基因在非裔美国男性中具有很强的相关性。本研究旨在评估 8q24 风险等位基因与临床变量(如病理分期、诊断时的年龄和复发)之间的关联,这些变量在一系列非裔美国男性病例中进行了评估。
114 名患有前列腺癌的非裔美国男性的外周血 DNA 样本,其中 106 名接受了根治性前列腺切除术,对三个 8q24 区域的六个单核苷酸多态性进行了基因分型。比较这些单核苷酸多态性与根治性前列腺切除术后的临床病理和随访数据。
诊断和随访时间的平均年龄分别为 57.4(+/-8.9)岁和 49.1(+/-31.6)个月。携带特定于非洲血统的 Broad11934905A 风险等位基因的患者,其病理分期(pT(3-4))高于野生型患者(优势比,4.48;95%置信区间,1.42-14.14;P = 0.011)。在 Kaplan-Meier 无调整生存分析中,携带该风险等位基因的患者的生化复发频率增加和时间缩短趋势(P = 0.076)。
8q24 上的 Broad11934905 多态性仅存在于非洲血统的人群中,与前列腺切除术后非器官受限的前列腺癌增加有关。此外,对于那些携带该风险等位基因的患者,生化复发的早期趋势需要在更大的研究中验证。