Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in Japanese

被引:100
作者
Akamatsu, Shusuke [1 ,2 ]
Takata, Ryo [1 ,3 ]
Haiman, Christopher A. [4 ]
Takahashi, Atsushi [5 ]
Inoue, Takahiro [2 ]
Kubo, Michiaki [6 ]
Furihata, Mutsuo [7 ]
Kamatani, Naoyuki [5 ]
Inazawa, Johji [8 ,9 ]
Chen, Gary K. [4 ]
Le Marchand, Loic [10 ]
Kolonel, Laurence N. [10 ]
Katoh, Takahiko [11 ]
Yamano, Yuko [12 ]
Yamakado, Minoru [13 ]
Takahashi, Hiroyuki [14 ]
Yamada, Hiroki [15 ]
Egawa, Shin [15 ]
Fujioka, Tomoaki [3 ]
Henderson, Brian E. [4 ]
Habuchi, Tomonori [16 ]
Ogawa, Osamu [2 ]
Nakamura, Yusuke [17 ]
Nakagawa, Hidewaki [1 ]
机构
[1] RIKEN, Ctr Genom Med, Lab Biomarker Dev, Tokyo, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Urol, Kyoto, Japan
[3] Iwate Med Univ, Dept Urol, Morioka, Iwate 020, Japan
[4] Univ So Calif, Keck Sch Med, Dept Prevent Med, Los Angeles, CA 90033 USA
[5] RIKEN, Ctr Genom Med, Lab Stat Anal, Yokohama, Kanagawa, Japan
[6] RIKEN, Ctr Genom Med, Lab Genotyping Dev, Tokyo, Japan
[7] Kochi Med Sch, Dept Pathol, Nankoku, Kochi, Japan
[8] Tokyo Med & Dent Univ, Med Res Inst, Dept Mol Cytogenet, Tokyo, Japan
[9] Tokyo Med & Dent Univ, Sch Biomed Sci, Tokyo, Japan
[10] Univ Hawaii, Canc Res Ctr, Program Epidemiol, Honolulu, HI 96813 USA
[11] Kumamoto Univ, Fac Hlth Sci, Dept Publ Hlth, Kumamoto, Japan
[12] Showa Univ, Sch Med, Dept Hyg & Prevent Med, Tokyo 142, Japan
[13] Mitsui Mem Hosp, Ctr Multiphas Hlth Testing & Serv, Tokyo 101, Japan
[14] Jikei Univ, Dept Pathol, Sch Med, Tokyo 105, Japan
[15] Jikei Univ, Sch Med, Dept Urol, Tokyo, Japan
[16] Akita Univ, Sch Med, Dept Urol, Akita 010, Japan
[17] Univ Tokyo, Inst Med Sci, Mol Med Lab, Ctr Human Genome, Tokyo, Japan
基金
美国国家卫生研究院; 日本学术振兴会;
关键词
GENOME-WIDE ASSOCIATION; SEQUENCE VARIANTS; ALLELIC LOSS; LOCI; GENE; IDENTIFICATION; REPLICATION; MUTATION; REGION; WDR11;
D O I
10.1038/ng.1104
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
We have previously reported multiple loci associated with prostate cancer susceptibility in a Japanese population using a genome-wide association study (GWAS). To identify additional prostate cancer susceptibility loci, we genotyped nine SNPs that were nominally associated with prostate cancer (P < 1 x 10(-4)) in our previous GWAS in three independent studies of prostate cancer in Japanese men (2,557 individuals with prostate cancer (cases) and 3,003 controls). In a meta-analysis of our previous GWAS and the replication studies, which included a total of 7,141 prostate cancer cases and 11,804 controls from a single ancestry group, three new loci reached genome-wide significance on chromosomes 11q12 (rs1938781; P = 1.10 x 10(-10); FAM111A-FAM111B), 10q26 (rs2252004; P = 1.98 x 10(-8)) and 3p11.2 (rs2055109; P = 3.94 x 10(-8)). We also found suggestive evidence of association at a previously reported prostate cancer susceptibility locus at 2p11 (rs2028898; P = 1.08 x 10(-7)). The identification of three new susceptibility loci should provide additional insight into the pathogenesis of prostate cancer and emphasizes the importance of conducting GWAS in diverse populations.
引用
收藏
页码:426 / U234
页数:5
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