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Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma.

Authors :
Jiang DK
Sun J
Cao G
Liu Y
Lin D
Gao YZ
Ren WH
Long XD
Zhang H
Ma XP
Wang Z
Jiang W
Chen TY
Gao Y
Sun LD
Long JR
Huang HX
Wang D
Yu H
Zhang P
Tang LS
Peng B
Cai H
Liu TT
Zhou P
Liu F
Lin X
Tao S
Wan B
Sai-Yin HX
Qin LX
Yin J
Liu L
Wu C
Pei Y
Zhou YF
Zhai Y
Lu PX
Tan A
Zuo XB
Fan J
Chang J
Gu X
Wang NJ
Li Y
Liu YK
Zhai K
Zhang H
Hu Z
Liu J
Yi Q
Xiang Y
Shi R
Ding Q
Zheng W
Shu XO
Mo Z
Shugart YY
Zhang XJ
Zhou G
Shen H
Zheng SL
Xu J
Yu L
Source :
Nature genetics [Nat Genet] 2013 Jan; Vol. 45 (1), pp. 72-5. Date of Electronic Publication: 2012 Dec 16.
Publication Year :
2013

Abstract

To identify genetic susceptibility loci for hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) in the Chinese population, we carried out a genome-wide association study (GWAS) in 2,514 chronic HBV carriers (1,161 HCC cases and 1,353 controls) followed by a 2-stage validation among 6 independent populations of chronic HBV carriers (4,319 cases and 4,966 controls). The joint analyses showed that HCC risk was significantly associated with two independent loci: rs7574865 at STAT4, P(meta) = 2.48 × 10(-10), odds ratio (OR) = 1.21; and rs9275319 at HLA-DQ, P(meta) = 2.72 × 10(-17), OR = 1.49. The risk allele G at rs7574865 was significantly associated with lower mRNA levels of STAT4 in both the HCC tissues and nontumor tissues of 155 individuals with HBV-related HCC (P(trend) = 0.0008 and 0.0002, respectively). We also found significantly lower mRNA expression of STAT4 in HCC tumor tissues compared with paired adjacent nontumor tissues (P = 2.33 × 10(-14)).

Details

Language :
English
ISSN :
1546-1718
Volume :
45
Issue :
1
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
23242368
Full Text :
https://doi.org/10.1038/ng.2483