Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population

被引:122
作者
Cui, R.
Okada, Y. [2 ]
Jang, S. G. [3 ]
Ku, J. L. [3 ]
Park, J. G. [3 ]
Kamatani, Y.
Hosono, N. [4 ]
Tsunoda, T. [5 ]
Kumar, V.
Tanikawa, C.
Kamatani, N. [6 ]
Yamada, R. [2 ]
Kubo, M. [4 ]
Nakamura, Y. [7 ]
Matsuda, K. [1 ]
机构
[1] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Lab Mol Med,Minato Ku, Tokyo 1088639, Japan
[2] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Lab Funct Genom, Tokyo 1088639, Japan
[3] Seoul Natl Univ, Coll Med, Canc Res Inst, Cell Biol Lab, Seoul, South Korea
[4] Inst Phys & Chem Res RIKEN, Ctr Genom Med, Lab Genotyping Dev, Kanagawa, Japan
[5] Inst Phys & Chem Res RIKEN, Ctr Genom Med, Lab Med Informat, Kanagawa, Japan
[6] Inst Phys & Chem Res RIKEN, Ctr Genom Med, Lab Stat Anal, Kanagawa, Japan
[7] Inst Phys & Chem Res RIKEN, Ctr Genom Med, Lab Int Alliance, Kanagawa, Japan
关键词
GENOME-WIDE ASSOCIATION; COLORECTAL-CANCER; ALCOHOL-CONSUMPTION; SUSCEPTIBILITY LOCUS; JAPANESE POPULATION; GENETIC-VARIANTS; INCIDENCE RATES; FAMILY HISTORY; RISK; SCAN;
D O I
10.1136/gut.2010.215947
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and aim Colorectal cancer (CRC) is a multifactorial disease with both environmental and genetic factors contributing to its development. The incidence of CRC is increasing year by year in Japan. Patients with CRC in advanced stages have a poor prognosis, but detection of CRC at earlier stages can improve clinical outcome. Therefore, identification of epidemiologial factors that influence development of CRC would facilitate the prevention or early detection of disease. Methods To identify loci associated with CRC risk, we performed a genome-wide association study (GWAS) for CRC and sub-analyses by tumour location using 1583 Japanese CRC cases and 1898 controls. Subsequently, we conducted replication analyses using a total of 4809 CRC cases and 2973 controls including 225 Korean subjects with distal colon cancer and 377 controls. Results We identified a novel locus on 6q26-q27 region (rs7758229 in SLC22A3, p=7.92x10(-9), OR of 1.28) that was significantly associated with distal colon cancer. We also replicated the association between CRC and SNPs on 8q24 (rs6983267 and rs7837328, p=1.51x10(-8) and 7.44x10(-8), ORs of 1.18 and 1.17, respectively). Moreover, we found cumulative effects of three genetic factors (rs7758229, rs6983267, and rs4939827 in SMAD7) and one environmental factor (alcohol drinking) which appear to increase CRC risk approximately twofold. Conclusions We found a novel susceptible locus in SLC22A3 that contributes to the risk of distal colon cancer in an Asian population. These findings would further extend our understanding of the role of common genetic variants in the aetiology of CRC.
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收藏
页码:799 / 805
页数:7
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