Single nucleotide polymorphisms in telomere length-related genes are associated with hepatocellular carcinoma risk in the Chinese Han population

被引:10
|
作者
Huang, Peng [1 ,2 ]
Li, Rong [3 ]
Shen, Lin [4 ]
He, Weizhou [5 ]
Chen, Shuo [1 ]
Dong, Yu [2 ]
Ma, Jiancang [1 ]
Chen, Xi [1 ]
Xu, Meng [1 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 2, Dept Gen Surg, Xian, Peoples R China
[2] Shaanxi Prov Corps Hosp Chinese Peoples Armed Pol, Dept Gen Surg, Xian, Shaanxi, Peoples R China
[3] Xi An Jiao Tong Univ, Affiliated Hosp 2, Dept Anesthesiol, Xian, Peoples R China
[4] Xi An Jiao Tong Univ, Affiliated Hosp 2, Dept Gastroenterol, Xian, Peoples R China
[5] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Hepatobiliary Surg, Xian, Peoples R China
基金
中国国家自然科学基金;
关键词
case-control study; gene variation; hepatocellular carcinoma; SNP; telomere length-related genes; GENOME-WIDE ASSOCIATION; PULMONARY-FIBROSIS; COMMON VARIANTS; PROSTATE-CANCER; ACYP2; SUSCEPTIBILITY; NUMBER; LOCUS; TERC;
D O I
10.1177/1758835920933029
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Single nucleotide polymorphisms (SNPs) in telomere-related genes are associated with a high risk of hepatocellular carcinoma (HCC). In this study, we investigated the SNPs of telomere length-related genes and their correlation with HCC risk in the Chinese Han population. Materials and methods: A total of 473 HCC patients and 564 healthy volunteers were recruited. Overall, 42 SNPs distributed in telomere-related genes were selected and identified. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated. Results: We found rs6713088 (OR = 1.27, 95% CI = 1.07-1.52,p = 0.007), rs843711 (OR = 1.29, 95% CI = 1.09-1.54,p = 0.004) and rs843706 (OR = 1.30, 95% CI = 1.09-1.55,p = 0.003) in theACYP2gene, rs10936599 (OR = 1.21, 95% CI = 1.02-1.44,p = 0.032) in theTERCgene and rs7708392 (OR = 1.24, 95% CI = 1.00-1.52,p = 0.042) in theTNIP1gene were associated with high HCC risk (OR > 1). In contrast, rs1682111 (OR = 0.77, 95% CI = 0.64-0.94,p = 0.008) in theACYP2gene, rs2320615 (OR = 0.79, 95% CI = 0.64-0.99,p = 0.038) in theNAF1gene, rs10069690 (OR = 0.75, 95% CI = 0.59-0.96,p = 0.021) and rs2242652 (OR = 0.70, 95% CI = 0.55-0.90,p = 0.004) in theTERTgene were associated with low HCC risk (OR < 1). Based on genotype frequency distributions, rs6713088, rs843645, rs843711 and rs843706 located in theACYP2gene as well as rs10936599 in theTERCgene were associated with a high incidence of HCC (p < 0.05). In addition, SNPs in these genes could form a linkage imbalance haplotype. Specifically, the haploid 'GC' formed by rs10069690 and rs2242652 within theTERTgene increased the risk of HCC (p < 0.05). Conclusion: SNPs inACYP2, TERC, TERTand other genes were correlated with HCC risk in the Chinese Han population. These data may provide new insights into early diagnosis and screening of HCC.
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页数:30
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