Sun Jielin, Zheng Siqun Lilly, Wiklund Fredrik, Isaacs Sarah D, Li Ge, Wiley Kathleen E, Kim Seong-Tae, Zhu Yi, Zhang Zheng, Hsu Fang-Chi, Turner Aubrey R, Stattin Pär, Liu Wennuan, Kim Jin Woo, Duggan David, Carpten John, Isaacs William, Grönberg Henrik, Xu Jianfeng, Chang Bao-Li
Center for Cancer Genomics, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Cancer Res. 2009 Jan 1;69(1):10-5. doi: 10.1158/0008-5472.CAN-08-3464.
To search for genetic variants that are associated with prostate cancer risk in the genome, we combined the data from our genome-wide association study (GWAS) in a population-based case-control study in Sweden with publicly available GWAS data from the Cancer Genetic Markers of Susceptibility (CGEMS) study. We limited the cases to those with aggressive disease in an attempt to identify risk variants that are associated with this most clinically relevant form of the disease. Among the most likely candidate single nucleotide polymorphisms (SNP) identified from the two GWAS, we sequentially confirmed one SNP at 22q13 in two independent study populations: the remaining subjects in Cancer of the Prostate in Sweden and a hospital-based case-control study at Johns Hopkins Hospital. Association of aggressive prostate cancer with the SNP at 22q13 was also observed in the publicly available data of four additional study populations from the second stage of the CGEMS study. In all seven study populations examined, the frequency of allele "C" of rs9623117 at 22q13 was consistently higher in aggressive cases than in controls. The combined allelic test was highly significant, with P = 5.0 x 10(-7). The odds ratio (OR) of allele C for aggressive prostate cancer was estimated to be 1.18 [95% confidence interval (95% CI), 1.11-1.26]. However, the SNP was also associated with nonaggressive prostate cancer, with an estimated OR of 1.11 (95% CI, 1.04-1.19; P = 0.004). The risk-associated variants are located within the genomic region of TNRC6B, a gene involved in miRNA-mediated mRNA degradation. Additional studies are warranted to further confirm the association.
为了在基因组中寻找与前列腺癌风险相关的基因变异,我们将瑞典一项基于人群的病例对照研究中的全基因组关联研究(GWAS)数据与癌症遗传易感性标记(CGEMS)研究中的公开GWAS数据相结合。我们将病例限定为患有侵袭性疾病的患者,试图识别与这种临床上最相关疾病形式相关的风险变异。在从两项GWAS中鉴定出的最有可能的候选单核苷酸多态性(SNP)中,我们在两个独立的研究人群中依次确认了位于22q13的一个SNP:瑞典前列腺癌研究中的其余受试者以及约翰霍普金斯医院的一项基于医院的病例对照研究。在CGEMS研究第二阶段另外四个研究人群的公开数据中也观察到侵袭性前列腺癌与22q13处的SNP之间存在关联。在所有七个研究人群中,22q13处rs9623117的等位基因“C”在侵袭性病例中的频率始终高于对照。联合等位基因检验具有高度显著性,P = 5.0×10⁻⁷。侵袭性前列腺癌等位基因C的优势比(OR)估计为1.18 [95%置信区间(95%CI),1.11 - 1.26]。然而,该SNP也与非侵袭性前列腺癌相关,估计OR为1.11(95%CI,1.04 - 1.19;P = 0.004)。与风险相关的变异位于TNRC6B基因的基因组区域内,该基因参与miRNA介导的mRNA降解。需要进一步的研究来进一步证实这种关联。