Association of CTLA4 gene +49G/A polymorphism with HBV infection and HBV-related hepatocellular carcinoma in Hunan Han population.
- Author:
Gang LIU
1
;
Guang-xiu LU
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Asian Continental Ancestry Group; genetics; CTLA-4 Antigen; genetics; Carcinoma, Hepatocellular; genetics; virology; Case-Control Studies; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Hepatitis B; genetics; Hepatitis B Surface Antigens; blood; Hepatitis B e Antigens; blood; Hepatitis B virus; Humans; Liver Neoplasms; genetics; virology; Male; Middle Aged; Polymorphism, Single Nucleotide
- From: Journal of Southern Medical University 2010;30(8):1838-1840
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the relationship between CTLA4 +49G/A SNP polymorphism and the susceptibility to hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC).
METHODSCTLA4+49G/A single nucleotide polymorphism (SNP) was analyzed by DNA sequencing in 165 control subjects, 155 patients with chronic hepatitis B (CHB) and 149 HCC patients. Serum HBsAg, HBeAg and AFP levels were measured in all the subjects.
RESULTSIn HCC and CHB groups, the genotype frequency was 40.3% and 50.0% for GG , and 59.7% and 50.0% for AG+AA, respectively, while the genotype frequency was 61.8% for GG and 38.2% for AG+AA in the control group. In HCC group, CHB group and controls, the A allele frequencies was 44.6%, 37.4% and 28.8%, and the G allele frequencies was 55.4%, 62.6% and 71.2%, respectively. Significant differences were found not only in the allele frequencies (P<0.05) but also in AA and combined (AA+AG) genotype frequencies (P<0.05) between the 3 groups.
CONCLUSION+49G/A SNP of the CTLA4 gene can be associated with HBV and HBV-related HCC.
