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A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma.

Authors :
Abnet CC
Freedman ND
Hu N
Wang Z
Yu K
Shu XO
Yuan JM
Zheng W
Dawsey SM
Dong LM
Lee MP
Ding T
Qiao YL
Gao YT
Koh WP
Xiang YB
Tang ZZ
Fan JH
Wang C
Wheeler W
Gail MH
Yeager M
Yuenger J
Hutchinson A
Jacobs KB
Giffen CA
Burdett L
Fraumeni JF Jr
Tucker MA
Chow WH
Goldstein AM
Chanock SJ
Taylor PR
Source :
Nature genetics [Nat Genet] 2010 Sep; Vol. 42 (9), pp. 764-7. Date of Electronic Publication: 2010 Aug 22.
Publication Year :
2010

Abstract

We conducted a genome-wide association study of gastric cancer and esophageal squamous cell carcinoma (ESCC) in ethnic Chinese subjects in which we genotyped 551,152 SNPs. We report a combined analysis of 2,240 gastric cancer cases, 2,115 ESCC cases and 3,302 controls drawn from five studies. In logistic regression models adjusted for age, sex and study, multiple variants at 10q23 had genome-wide significance for gastric cancer and ESCC independently. A notable signal was rs2274223, a nonsynonymous SNP located in PLCE1, for gastric cancer (P = 8.40 x 10(-9); per-allele odds ratio (OR) = 1.31) and ESCC (P = 3.85 x 10(-9); OR = 1.34). The association with gastric cancer differed by anatomic subsite. For tumors in the cardia the association was stronger (P = 4.19 x 10(-15); OR = 1.57), and for those in the noncardia stomach it was absent (P = 0.44; OR = 1.05). Our findings at 10q23 could provide insight into the high incidence of both cancers in China.

Details

Language :
English
ISSN :
1546-1718
Volume :
42
Issue :
9
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
20729852
Full Text :
https://doi.org/10.1038/ng.649