Two novel polymorphisms in PLCE1 are associated with the susceptibility to esophageal squamous cell carcinoma in Chinese population

被引:9
作者
Qu, Y. [1 ,2 ]
Zhang, S. [1 ,2 ]
Cui, L. [3 ]
Wang, K. [1 ,2 ]
Song, C. [1 ,2 ]
Wang, P. [1 ,2 ]
Zhang, J. [1 ,2 ]
Dai, L. [1 ,2 ]
机构
[1] Zhengzhou Univ, Coll Publ Hlth, Dept Epidemiol & Biostat, 100 Sci Ave, Zhengzhou 450001, Peoples R China
[2] Key Lab Tumor Epidemiol, Zhengzhou, Peoples R China
[3] Navy Gen Hosp, Dept Digest Syst, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
esophageal squamous cell carcinoma; PLCE1; polymorphism; susceptibility; GENOME-WIDE ASSOCIATION; GASTRIC-CANCER; GENETIC-VARIANTS; RISK; 10Q23; EXPRESSION; ALCOHOL; TOBACCO; 1Q22; LOCI;
D O I
10.1111/dote.12463
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Esophageal cancer is the sixth leading cause of cancer-associated death worldwide. Phospholipase C epsilon 1 (PLCE1) gene was found to be associated with the risk of esophageal squamous cell carcinoma (ESCC) by three large-scale genome-wide association studies (GWAS) in Chinese populations. To evaluate the association between the single nucleotide polymorphisms (SNPs) in PLCE1 gene and ESCC risk, a case-control study including 550 patients with ESCC and 550 age, gender-matched controls was carried out to investigate the genetic susceptibility of three SNPs (rs3765524 C/T and two unreported potentially functional SNPs rs10882379 G/A and rs829232 G/A) as well as the interactions of gene-gene and gene-environment in the development of ESCC. And the results showed that GA genotype of rs10882379 was significantly associated with reduced ESCC risk compared with GG genotype (adjusted OR [95% CI]: 0.66 [0.51, 0.86]), while AA genotype of rs829232 was significantly associated with increased ESCC risk compared with GG genotype (adjusted OR [95% CI]: 1.37 [1.12, 1.67]). The haplotype analysis showed increased ESCC risk in G(rs10882379)C(rs3765524)A(rs829232) and G(rs10882379)T(rs3765524)A(rs829232) haplotypes with OR (95% CI) of 1.40 (1.13, 1.73) and 1.66 (1.18, 2.34), respectively and inversely reduced ESCC risk in A(rs10882379)C(rs3765524)G(rs829232) haplotype with OR (95% CI) of 0.74 (0.61, 0.91). The gene-environment interaction analysis emerged a best model consisted of four factors (rs10882379, rs3765524, rs829232 and family history of ESCC) that could increase the ESCC risk in the 'high risk group' with 4.45-fold (OR [95% CI]: 5.45 [4.13, 7.19]), compared to the 'low risk group.' Our results further validate that the SNPs in PLCE1 gene may contribute to the ESCC susceptibility in Chinese Han population. Also the gene-gene and gene-environment interactions play a certain crucial role in the ESCC progression.
引用
收藏
页码:1 / 7
页数:7
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