Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus–related hepatocellular carcinoma
Long Yu and colleagues report a genome-wide association study for hepatitis B virus–related hepatocellular carcinoma (HBV-HCC). They report that genetic variants in STAT4 and HLA-DQ genes confer risk of HBV-HCC. To identify genetic susceptibility loci for hepatitis B virus (HBV)-related hepatocellul...
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Published in | Nature genetics Vol. 45; no. 1; pp. 72 - 75 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Nature Publishing Group US
01.01.2013
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | Long Yu and colleagues report a genome-wide association study for hepatitis B virus–related hepatocellular carcinoma (HBV-HCC). They report that genetic variants in
STAT4
and HLA-DQ genes confer risk of HBV-HCC.
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
). |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 These authors jointly directed this work. These authors contributed equally to this work. |
ISSN: | 1061-4036 1546-1718 1546-1718 |
DOI: | 10.1038/ng.2483 |