TY - JOUR
T1 - MicroRNA-196A-2 polymorphisms and hepatocellular carcinoma in patients with chronic hepatitis B
AU - Kim, Hwi Young
AU - Yoon, Jung Hwan
AU - Lee, Hyo Suk
AU - Cheong, Jae Youn
AU - Cho, Sung Won
AU - Shin, Hyoung Doo
AU - Kim, Yoon Jun
PY - 2014/3
Y1 - 2014/3
N2 - Single nucleotide polymorphisms (SNPs) in microRNA (miR)-196a-2 have been suggested to contribute to susceptibility to various human cancers. The aim of this study was to determine whether polymorphisms of miRNA-196a-2 affect the clinical outcomes of hepatitis B virus (HBV) infection in Korean patients. Genotyping was performed for 1,439 Korean patients with either past or present HBV infection, including 404 control subjects who underwent spontaneous recovery and 1,035 subjects with chronic HBV (313 cases of chronic hepatitis B, 305 cases of cirrhosis of the liver, and 417 cases of hepatocellular carcinoma [HCC]). Genotyping results revealed that the polymorphism rs12304647A>C, which lies in the pri-miRNA region of miR-196a-2, has a significant minor allele frequency (0.210). Logistic analysis revealed that the rs12304647A>C SNP was associated with a significant protective effect against HCC in patients with chronic hepatitis (odds ratio [OR]=0.70, P=0.005 in a codominant model; OR=0.73, P=0.03 in a dominant model; OR=0.31, P=0.004 in a recessive model), and in the patients with cirrhosis (OR=0.63, P=0.0009 in a codominant model; OR=0.66, P=0.01 in a dominant model; OR=0.25, P=0.001 in a recessive model). A Cox relative hazards model with adjustments for age, gender, HBeAg status, and cirrhosis revealed that rs12304647A>C retained its association with HCC in a codominant model (relative hazards [RH]=1.14, P=0.05) and in a recessive model (RH=1.44, P=0.03). However, the miR-196a-2 rs12304647A>C SNP had no association with HBV clearance. In conclusion, the miR-196a-2 rs12304647 CC genotype had a protective effect against development of HCC in comparison to the AA or AC genotypes in patients with chronic hepatitis and cirrhosis. J. Med. Virol. 86:446-453, 2014.
AB - Single nucleotide polymorphisms (SNPs) in microRNA (miR)-196a-2 have been suggested to contribute to susceptibility to various human cancers. The aim of this study was to determine whether polymorphisms of miRNA-196a-2 affect the clinical outcomes of hepatitis B virus (HBV) infection in Korean patients. Genotyping was performed for 1,439 Korean patients with either past or present HBV infection, including 404 control subjects who underwent spontaneous recovery and 1,035 subjects with chronic HBV (313 cases of chronic hepatitis B, 305 cases of cirrhosis of the liver, and 417 cases of hepatocellular carcinoma [HCC]). Genotyping results revealed that the polymorphism rs12304647A>C, which lies in the pri-miRNA region of miR-196a-2, has a significant minor allele frequency (0.210). Logistic analysis revealed that the rs12304647A>C SNP was associated with a significant protective effect against HCC in patients with chronic hepatitis (odds ratio [OR]=0.70, P=0.005 in a codominant model; OR=0.73, P=0.03 in a dominant model; OR=0.31, P=0.004 in a recessive model), and in the patients with cirrhosis (OR=0.63, P=0.0009 in a codominant model; OR=0.66, P=0.01 in a dominant model; OR=0.25, P=0.001 in a recessive model). A Cox relative hazards model with adjustments for age, gender, HBeAg status, and cirrhosis revealed that rs12304647A>C retained its association with HCC in a codominant model (relative hazards [RH]=1.14, P=0.05) and in a recessive model (RH=1.44, P=0.03). However, the miR-196a-2 rs12304647A>C SNP had no association with HBV clearance. In conclusion, the miR-196a-2 rs12304647 CC genotype had a protective effect against development of HCC in comparison to the AA or AC genotypes in patients with chronic hepatitis and cirrhosis. J. Med. Virol. 86:446-453, 2014.
KW - Hepatitis B
KW - Liver cancer
KW - MicroRNA
KW - Polymorphism
UR - http://www.scopus.com/inward/record.url?scp=84891926518&partnerID=8YFLogxK
U2 - 10.1002/jmv.23848
DO - 10.1002/jmv.23848
M3 - Article
C2 - 24248733
AN - SCOPUS:84891926518
SN - 0146-6615
VL - 86
SP - 446
EP - 453
JO - Journal of Medical Virology
JF - Journal of Medical Virology
IS - 3
ER -