Literature DB >> 31826910

Identification of Novel Loci and New Risk Variant in Known Loci for Colorectal Cancer Risk in East Asians.

Yingchang Lu1, Sun-Seog Kweon2,3, Qiuyin Cai1, Chizu Tanikawa4, Xiao-Ou Shu1, Wei-Hua Jia5, Yong-Bing Xiang6, Jeroen R Huyghe7, Tabitha A Harrison7, Jeongseon Kim8, Aesun Shin9, Dong-Hyun Kim10, Keitaro Matsuo11,12, Sun Ha Jee13, Xingyi Guo1, Wanqing Wen1, Jiajun Shi1, Bingshan Li14, Nan Wang15, Min-Ho Shin2, Hong-Lan Li6, Zefang Ren16, Jae Hwan Oh17, Isao Oze10, Yoon-Ok Ahn18, Keum Ji Jung19, Jing Gao6, Yu-Tang Gao6, Zhi-Zhong Pan5, Yoichiro Kamatani20,21, Andrew T Chan22,23,24,25, Andrea Gsur26, Jochen Hampe27, Loic Le Marchand28, Li Li29, Annika Lindblom30,31, Victor Moreno32,33,34, Polly A Newcomb7,35, Kenneth Offit36,37, Paul D P Pharoah38, Franzel J B van Duijnhoven39, Bethany Van Guelpen40, Pavel Vodicka41,42,43, Stephanie J Weinstein44, Alicja Wolk45, Anna H Wu46, Li Hsu7,47, Yi-Xin Zeng5, Jirong Long1, Ulrike Peters7,48, Koichi Matsuda49, Wei Zheng50.   

Abstract

BACKGROUND: Risk variants identified so far for colorectal cancer explain only a small proportion of familial risk of this cancer, particularly in Asians.
METHODS: We performed a genome-wide association study (GWAS) of colorectal cancer in East Asians, including 23,572 colorectal cancer cases and 48,700 controls. To identify novel risk loci, we selected 60 promising risk variants for replication using data from 58,131 colorectal cancer cases and 67,347 controls of European descent. To identify additional risk variants in known colorectal cancer loci, we performed conditional analyses in East Asians.
RESULTS: An indel variant, rs67052019 at 1p13.3, was found to be associated with colorectal cancer risk at P = 3.9 × 10-8 in Asians (OR per allele deletion = 1.13, 95% confidence interval = 1.08-1.18). This association was replicated in European descendants using a variant (rs2938616) in complete linkage disequilibrium with rs67052019 (P = 7.7 × 10-3). Of the remaining 59 variants, 12 showed an association at P < 0.05 in the European-ancestry study, including rs11108175 and rs9634162 at P < 5 × 10-8 and two variants with an association near the genome-wide significance level (rs60911071, P = 5.8 × 10-8; rs62558833, P = 7.5 × 10-8) in the combined analyses of Asian- and European-ancestry data. In addition, using data from East Asians, we identified 13 new risk variants at 11 loci reported from previous GWAS.
CONCLUSIONS: In this large GWAS, we identified three novel risk loci and two highly suggestive loci for colorectal cancer risk and provided evidence for potential roles of multiple genes and pathways in the etiology of colorectal cancer. In addition, we showed that additional risk variants exist in many colorectal cancer risk loci identified previously. IMPACT: Our study provides novel data to improve the understanding of the genetic basis for colorectal cancer risk. ©2019 American Association for Cancer Research.

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Year:  2019        PMID: 31826910      PMCID: PMC7571256          DOI: 10.1158/1055-9965.EPI-19-0755

Source DB:  PubMed          Journal:  Cancer Epidemiol Biomarkers Prev        ISSN: 1055-9965            Impact factor:   4.254


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