Cargando…
Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study
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 (GW...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727098/ https://www.ncbi.nlm.nih.gov/pubmed/26870257 http://dx.doi.org/10.3892/ol.2015.3958 |
_version_ | 1782411922819252224 |
---|---|
author | QU, LI-SHUAI JIN, FEI GUO, YAN-MEI LIU, TAO-TAO XUE, RU-YI HUANG, XIAO-WU XU, MIN CHEN, TAO-YANG NI, ZHENG-PING SHEN, XI-ZHONG |
author_facet | QU, LI-SHUAI JIN, FEI GUO, YAN-MEI LIU, TAO-TAO XUE, RU-YI HUANG, XIAO-WU XU, MIN CHEN, TAO-YANG NI, ZHENG-PING SHEN, XI-ZHONG |
author_sort | QU, LI-SHUAI |
collection | PubMed |
description | 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 GeneChip 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 GoldenGate 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)=5.23×10(−8); OR(allele)=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 OR(allele)=1.76; 95% CI, 1.39–2.22; P=2.00×10(−6)), which maps within the fourth intron of VEPH1. The second strongest statistical evidence for an association was identified for rs1350171 (combined OR(allele)=1.66; 95% CI, 1.33–2.07; P=6.48×10(−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 β, insulin/phosphoinositide 3 kinase, Wnt and epidermal growth factor receptor. These associations must be replicated and validated in larger studies. |
format | Online Article Text |
id | pubmed-4727098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-47270982016-02-11 Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study QU, LI-SHUAI JIN, FEI GUO, YAN-MEI LIU, TAO-TAO XUE, RU-YI HUANG, XIAO-WU XU, MIN CHEN, TAO-YANG NI, ZHENG-PING SHEN, XI-ZHONG Oncol Lett Articles 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 GeneChip 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 GoldenGate 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)=5.23×10(−8); OR(allele)=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 OR(allele)=1.76; 95% CI, 1.39–2.22; P=2.00×10(−6)), which maps within the fourth intron of VEPH1. The second strongest statistical evidence for an association was identified for rs1350171 (combined OR(allele)=1.66; 95% CI, 1.33–2.07; P=6.48×10(−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 β, insulin/phosphoinositide 3 kinase, Wnt and epidermal growth factor receptor. These associations must be replicated and validated in larger studies. D.A. Spandidos 2016-01 2015-11-23 /pmc/articles/PMC4727098/ /pubmed/26870257 http://dx.doi.org/10.3892/ol.2015.3958 Text en Copyright: © Qu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles QU, LI-SHUAI JIN, FEI GUO, YAN-MEI LIU, TAO-TAO XUE, RU-YI HUANG, XIAO-WU XU, MIN CHEN, TAO-YANG NI, ZHENG-PING SHEN, XI-ZHONG Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study |
title | Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study |
title_full | Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study |
title_fullStr | Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study |
title_full_unstemmed | Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study |
title_short | Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study |
title_sort | nine susceptibility loci for hepatitis b virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727098/ https://www.ncbi.nlm.nih.gov/pubmed/26870257 http://dx.doi.org/10.3892/ol.2015.3958 |
work_keys_str_mv | AT qulishuai ninesusceptibilitylociforhepatitisbvirusrelatedhepatocellularcarcinomaidentifiedbyapilottwostagegenomewideassociationstudy AT jinfei ninesusceptibilitylociforhepatitisbvirusrelatedhepatocellularcarcinomaidentifiedbyapilottwostagegenomewideassociationstudy AT guoyanmei ninesusceptibilitylociforhepatitisbvirusrelatedhepatocellularcarcinomaidentifiedbyapilottwostagegenomewideassociationstudy AT liutaotao ninesusceptibilitylociforhepatitisbvirusrelatedhepatocellularcarcinomaidentifiedbyapilottwostagegenomewideassociationstudy AT xueruyi ninesusceptibilitylociforhepatitisbvirusrelatedhepatocellularcarcinomaidentifiedbyapilottwostagegenomewideassociationstudy AT huangxiaowu ninesusceptibilitylociforhepatitisbvirusrelatedhepatocellularcarcinomaidentifiedbyapilottwostagegenomewideassociationstudy AT xumin ninesusceptibilitylociforhepatitisbvirusrelatedhepatocellularcarcinomaidentifiedbyapilottwostagegenomewideassociationstudy AT chentaoyang ninesusceptibilitylociforhepatitisbvirusrelatedhepatocellularcarcinomaidentifiedbyapilottwostagegenomewideassociationstudy AT nizhengping ninesusceptibilitylociforhepatitisbvirusrelatedhepatocellularcarcinomaidentifiedbyapilottwostagegenomewideassociationstudy AT shenxizhong ninesusceptibilitylociforhepatitisbvirusrelatedhepatocellularcarcinomaidentifiedbyapilottwostagegenomewideassociationstudy |