Genetic variation in 8q24 associated with risk of colorectal cancer

被引:56
作者
Gruber, Stephen B.
Moreno, Victor
Rozek, Laura S.
Rennert, Hedy S.
Lejbkowicz, Flavio
Bonner, Joseph D.
Greenson, Joel K.
Giordano, Thomas J.
Fearon, Eric R.
Rennert, Gad
机构
[1] Univ Michigan, Sch Med, Dept Internal Med, Div Med & Mol Genet, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Epidemiol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USA
[4] Catalan Inst Oncol, Barcelona, Spain
[5] Technion Israel Inst Technol, Carmel Med Ctr, Haifa, Israel
[6] Technion Israel Inst Technol, Bruce Rappaport Fac Med, IL-31096 Haifa, Israel
[7] Technion Israel Inst Technol, CHS Natl Canc Control Ctr, IL-31096 Haifa, Israel
[8] Technion Israel Inst Technol, Dept Community Med & Epidemiol, IL-31096 Haifa, Israel
[9] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
关键词
colorectal cancer; genetics; epidemiology; risk; kin-cohort analysis;
D O I
10.4161/cbt.6.7.4704
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chromosome 8q24 harbors oncogenes known to be involved in pathogenesis of colorectal cancer (CRC) as well as uncharacterized genetic variants that have recently been shown to influence inherited risk of prostate cancer. In a population-based case-control study of colorectal cancer in northern Israel, we investigated the association between variation in 8q24 and risk of CRC. Among 1,861 incident cases and 1,937 population-based controls matched on age, gender, ethnicity, and clinic, rs 10505477 was associated with risk of CRC in a dominant model, with an odds ratio = 1.23, 95% confidence interval = 1.05-1.43, (p = 0.008). This association was independently validated in an analysis of cancer among relatives of carriers of the risk allele, with a hazard ratio of 3.2 (95% bootstrap CI = 1.16-17.8). Genetic variation at rs 10505477 on 8q24 potentially accounts for 14% of CRC in this population and should be replicated in other studies.
引用
收藏
页码:1143 / 1147
页数:5
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