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Correlation between the DEPDC5 rs1012068 polymorphism and the risk of HBV-related hepatocellular carcinoma
Wenxuan Liu1, Ning Ma1, Dongqiang Zhao2
1Department of Epidemiology and Statistics, School of Public Health, Hebei Medical University, Hebei Key Laboratory of Environment and Human health, Shi Jiazhuang, PR China.
Insights
Hepatocellular carcinoma (HCC) risk is linked to a common genetic variant, DEPDC5 rs1012068, in the Han Chinese population. The A to C mutation in DEPDC5 increases the likelihood of developing Hepatitis B virus (HBV)-related HCC.
Area of Science:
- Genetics
- Hepatology
- Cancer Research
Background:
- Hepatocellular carcinoma (HCC) is primarily caused by Hepatitis B virus (HBV) or Hepatitis C virus (HCV) infection.
- The precise molecular mechanisms by which HBV contributes to HCC development remain unclear.
- A 2011 genome-wide association study (GWAS) identified a DEPDC5 gene variant associated with HCC susceptibility in HCV-infected patients.
Purpose of the Study:
- To investigate the association between DEPDC5 gene polymorphism and HBV-related HCC.
- To determine if DEPDC5 rs1012068 variants influence HCC risk in the Han Chinese population.
Main Methods:
- A cohort of 1289 individuals from northern China was studied, including healthy controls, patients with chronic Hepatitis B (CHB), liver cirrhosis (LC), and HBV-related HCC.
- Single nucleotide polymorphisms (SNPs) in DEPDC5 rs1012068 were genotyped using MALDI-TOF-MS.
- Statistical analyses controlled for factors such as sex, smoking, and alcohol consumption.
Main Results:
- A significant correlation was found between DEPDC5 rs1012068 polymorphism and HBV-related HCC.
- Individuals with the CC genotype had a 2.008-fold increased risk of HCC compared to controls.
- The CC genotype was also associated with increased risk in CHB (2.241-fold) and LC (2.706-fold) patients.
- The AC genotype showed a 1.615-fold increased risk of HCC.
Conclusions:
- The DEPDC5 rs1012068 A/C polymorphism is significantly associated with HBV-related HCC in the Han Chinese population.
- The A to C mutation within DEPDC5 rs1012068 appears to elevate the risk of developing HBV-related HCC.
Introduction:
HBV and/or HCV infection is the main cause of hepatocellular carcinoma (HCC), but the molecular mechanisms by which HBV promotes HCC are not clear. In 2011, the result of a GWAS revealed a common variant of DEPDC5 affected HCC susceptibility in patient with chronic HCV infection in Japan. This study investigated the correlation between DEPDC5 polymorphism and HBV-related HCC.
Materials And Methods:
1289 samples of Han population were involved in northern China and peripheral blood samples were obtained, including 506 healthy controls, 217 Hepatitis B chronic (CHB) and 258 liver cirrhosis (LC), and 308 HBV-related HCC patients. SNPs in the DEPDC5 rs1012068 were detected by MALDI-TOF-MS.
Results:
After controlling for the influence of sex, smoking and drinking, this study showed a significant relationship between the polymorphism of DEPDC5 rs1012068 and HBV-related HCC. Healthy participants with CC genotype showed 2.008 (95% CI = 1.145, 3.520; P = 0.015) times more likely to develop HCC; CHB cases with CC genotype showed 2.241 (95% CI = 1.226, 4.461; P = 0.022) times more likely to develop HCC; LC cases with CC genotype showed 2.706 (95% CI = 1.371, 5.340; P = 0.004) times more likely to develop HCC; and individuals with AC genotype showed 1.615 (95% CI = 1.110, 2.352; P = 0.012) times more likely to develop HCC.
Conclusions:
There was a significant correlation between DEPDC5 rs1012068A/C and HBV-related HCC in the Han Chinese population. A to C mutation increased the risk of the developing of HBV-related HCC.
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