4.4 Article

Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage, genome-wide association study

期刊

ONCOLOGY LETTERS
卷 11, 期 1, 页码 624-632

出版社

SPANDIDOS PUBL LTD
DOI: 10.3892/ol.2015.3958

关键词

single-nucleotide polymorphisms; hepatitis B virus; hepatocellular carcinoma

类别

资金

  1. China Ministry of Health [W201202]
  2. National Natural Science Foundation [81302056]
  3. Natural Science Foundation of Jiangsu Province [BK2012225]
  4. Foundation of Jiangsu Province [WS056]

向作者/读者索取更多资源

Previous studies have indicated that complex interactions among viral, environmental and genetic factors lead to hepatocellular carcinoma (HCC). To identify susceptibility alleles for hepatitis B virus (HBV)-related HCC, the present study conducted a pilot two-phase genome-wide association study (GWAS) in 660 Han Chinese individuals. In phase 1, a total of 500,447 single-nucleotide polymorphisms (SNPs) were genotyped in 50 HCC cases and 50 controls using Affymetrix Gene Chip 500k Array Set. In phase 2, 1,152 SNPs were selected from phase 1 and genotyped in 282 cases and 278 controls using the Illumina Golden Gate platform. The prior probability of HCC in control subjects was assigned at 0.01, and false-positive report probability (FPRP) was utilized to evaluate the statistical significance. In phase 1, one SNP (rs2212522) showed a significant association with HCC (P-allele=5.23x10(-8); ORallele=4.96; 95% CI, 2.72-9.03). In phase 2, among 27 SNPs with unadjusted P-allele <0.05, 9 SNPs were associated with HCC based on FPRP criteria (FPRP <0.20). The strongest statistical evidence for an association signal was with rs2120243 (combined ORallele=1.76; 95% CI, 1.39-2.22; P=2.00x10(-6)), which maps within the fourth intron of VEPH1. The second strongest statistical evidence for an association was identified for rs1350171 (combined ORallele=1.66; 95% CI, 1.33-2.07; P.=6.48x10(-6)), which maps to the region downstream of the FZD4 gene. The other potential susceptibility genes included PCDH9, PRMT6, LHX1, KIF2B and L3MBTL4. In conclusion, this pilot two-phase GWAS provides the evidence for the existence of common susceptibility loci for HCC. These genes involved various signaling pathways, including those associated with transforming growth factor 13, insulin/phosphoinositide 3 kinase, Wnt and epidermal growth factor receptor. These associations must be replicated and validated in larger studies.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据