File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1038/ng.2424
- Scopus: eid_2-s2.0-84868206960
- PMID: 23023329
- WOS: WOS:000310495800015
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4
Title | Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4 |
---|---|
Authors | Xu, JianfengMo, ZengnanYe, DingweiWang, MeilinLiu, FangJin, GuangfuXu, ChuanliangWang, XiangShao, QiangChen, ZhiwenTao, ZhihuaQi, JunZhou, FangjianWang, ZhongFu, YaowenHe, DalinWei, QiangGuo, JianmingWu, DenglongGao, XinYuan, JianlinWang, GongxianXu, YongWang, GuozengYao, HaijunDong, PeiJiao, YangShen, MoYang, JinOu-Yang, JunJiang, HaowenZhu, YaoRen, ShanchengZhang, ZhengdongYin, ChangjunGao, XuDai, BoHu, ZhibinYang, YajunWu, QijunChen, HongyanPeng, PengZheng, YingZheng, XiaodongXiang, YongbingLong, JirongGong, JianNa, RongLin, XiaolingYu, HongjieWeng, ZhongTao, ShaFeng, JunjieSun, JishanLiu, WennuanHsing, AnnRao, JianyuDing, QiangWikland, FredirikGronberg, HenrikShu, Xiao OuZheng, WeiShen, HongbingJin, LiShi, RongLu, DaruZhang, XuejunSun, JielinLilly Zheng, S.Sun, Yinghao |
Issue Date | 2012 |
Citation | Nature Genetics, 2012, v. 44, n. 11, p. 1231-1235 How to Cite? |
Abstract | Prostate cancer risk-associated variants have been reported in populations of European descent, African-Americans and Japanese using genome-wide association studies (GWAS). To systematically investigate prostate cancer risk-associated variants in Chinese men, we performed the first GWAS in Han Chinese. In addition to confirming several associations reported in other ancestry groups, this study identified two new risk-associated loci for prostate cancer on chromosomes 9q31.2 (rs817826, P = 5.45 × 10-14) and 19q13.4 (rs103294, P = 5.34 × 10-16) in 4,484 prostate cancer cases and 8,934 controls. The rs103294 marker at 19q13.4 is in strong linkage equilibrium with a 6.7-kb germline deletion that removes the first six of seven exons in LILRA3, a gene regulating inflammatory response, and was significantly associated with the mRNA expression of LILRA3 in T cells (P < 1 × 10-4). These findings may advance the understanding of genetic susceptibility to prostate cancer. © 2012 Nature America, Inc. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/314343 |
ISSN | 2023 Impact Factor: 31.7 2023 SCImago Journal Rankings: 17.300 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Xu, Jianfeng | - |
dc.contributor.author | Mo, Zengnan | - |
dc.contributor.author | Ye, Dingwei | - |
dc.contributor.author | Wang, Meilin | - |
dc.contributor.author | Liu, Fang | - |
dc.contributor.author | Jin, Guangfu | - |
dc.contributor.author | Xu, Chuanliang | - |
dc.contributor.author | Wang, Xiang | - |
dc.contributor.author | Shao, Qiang | - |
dc.contributor.author | Chen, Zhiwen | - |
dc.contributor.author | Tao, Zhihua | - |
dc.contributor.author | Qi, Jun | - |
dc.contributor.author | Zhou, Fangjian | - |
dc.contributor.author | Wang, Zhong | - |
dc.contributor.author | Fu, Yaowen | - |
dc.contributor.author | He, Dalin | - |
dc.contributor.author | Wei, Qiang | - |
dc.contributor.author | Guo, Jianming | - |
dc.contributor.author | Wu, Denglong | - |
dc.contributor.author | Gao, Xin | - |
dc.contributor.author | Yuan, Jianlin | - |
dc.contributor.author | Wang, Gongxian | - |
dc.contributor.author | Xu, Yong | - |
dc.contributor.author | Wang, Guozeng | - |
dc.contributor.author | Yao, Haijun | - |
dc.contributor.author | Dong, Pei | - |
dc.contributor.author | Jiao, Yang | - |
dc.contributor.author | Shen, Mo | - |
dc.contributor.author | Yang, Jin | - |
dc.contributor.author | Ou-Yang, Jun | - |
dc.contributor.author | Jiang, Haowen | - |
dc.contributor.author | Zhu, Yao | - |
dc.contributor.author | Ren, Shancheng | - |
dc.contributor.author | Zhang, Zhengdong | - |
dc.contributor.author | Yin, Changjun | - |
dc.contributor.author | Gao, Xu | - |
dc.contributor.author | Dai, Bo | - |
dc.contributor.author | Hu, Zhibin | - |
dc.contributor.author | Yang, Yajun | - |
dc.contributor.author | Wu, Qijun | - |
dc.contributor.author | Chen, Hongyan | - |
dc.contributor.author | Peng, Peng | - |
dc.contributor.author | Zheng, Ying | - |
dc.contributor.author | Zheng, Xiaodong | - |
dc.contributor.author | Xiang, Yongbing | - |
dc.contributor.author | Long, Jirong | - |
dc.contributor.author | Gong, Jian | - |
dc.contributor.author | Na, Rong | - |
dc.contributor.author | Lin, Xiaoling | - |
dc.contributor.author | Yu, Hongjie | - |
dc.contributor.author | Weng, Zhong | - |
dc.contributor.author | Tao, Sha | - |
dc.contributor.author | Feng, Junjie | - |
dc.contributor.author | Sun, Jishan | - |
dc.contributor.author | Liu, Wennuan | - |
dc.contributor.author | Hsing, Ann | - |
dc.contributor.author | Rao, Jianyu | - |
dc.contributor.author | Ding, Qiang | - |
dc.contributor.author | Wikland, Fredirik | - |
dc.contributor.author | Gronberg, Henrik | - |
dc.contributor.author | Shu, Xiao Ou | - |
dc.contributor.author | Zheng, Wei | - |
dc.contributor.author | Shen, Hongbing | - |
dc.contributor.author | Jin, Li | - |
dc.contributor.author | Shi, Rong | - |
dc.contributor.author | Lu, Daru | - |
dc.contributor.author | Zhang, Xuejun | - |
dc.contributor.author | Sun, Jielin | - |
dc.contributor.author | Lilly Zheng, S. | - |
dc.contributor.author | Sun, Yinghao | - |
dc.date.accessioned | 2022-07-20T12:03:41Z | - |
dc.date.available | 2022-07-20T12:03:41Z | - |
dc.date.issued | 2012 | - |
dc.identifier.citation | Nature Genetics, 2012, v. 44, n. 11, p. 1231-1235 | - |
dc.identifier.issn | 1061-4036 | - |
dc.identifier.uri | http://hdl.handle.net/10722/314343 | - |
dc.description.abstract | Prostate cancer risk-associated variants have been reported in populations of European descent, African-Americans and Japanese using genome-wide association studies (GWAS). To systematically investigate prostate cancer risk-associated variants in Chinese men, we performed the first GWAS in Han Chinese. In addition to confirming several associations reported in other ancestry groups, this study identified two new risk-associated loci for prostate cancer on chromosomes 9q31.2 (rs817826, P = 5.45 × 10-14) and 19q13.4 (rs103294, P = 5.34 × 10-16) in 4,484 prostate cancer cases and 8,934 controls. The rs103294 marker at 19q13.4 is in strong linkage equilibrium with a 6.7-kb germline deletion that removes the first six of seven exons in LILRA3, a gene regulating inflammatory response, and was significantly associated with the mRNA expression of LILRA3 in T cells (P < 1 × 10-4). These findings may advance the understanding of genetic susceptibility to prostate cancer. © 2012 Nature America, Inc. All rights reserved. | - |
dc.language | eng | - |
dc.relation.ispartof | Nature Genetics | - |
dc.title | Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4 | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1038/ng.2424 | - |
dc.identifier.pmid | 23023329 | - |
dc.identifier.pmcid | PMC4116636 | - |
dc.identifier.scopus | eid_2-s2.0-84868206960 | - |
dc.identifier.volume | 44 | - |
dc.identifier.issue | 11 | - |
dc.identifier.spage | 1231 | - |
dc.identifier.epage | 1235 | - |
dc.identifier.eissn | 1546-1718 | - |
dc.identifier.isi | WOS:000310495800015 | - |