TY - JOUR
T1 - DNA binding protein A expression and methylation status in hepatocellular carcinoma and the adjacent tissue
AU - Yasen, Mahmut
AU - Obulhasim, Gulanbar
AU - Kajino, Kazunori
AU - Mogushi, Kaoru
AU - Mizushima, Hiroshi
AU - Tanaka, Shinji
AU - Tanaka, Hiroshi
AU - Hino, Okio
AU - Arii, Shigeki
PY - 2012/3
Y1 - 2012/3
N2 - We investigated the expression and promoter methylation of dbpA in human hepatocellular carcinoma (HCC) and examined their correlation with clinicophathological features. In 96 paired samples of HCC and adjacent non-tumorous liver, and 10 normal liver specimens, dbpA mRNA was quantified by real-time RT-PCR, and promoter methylation was examined by methylation-specific polymerase chain reaction and bisulfite sequencing. The results showed that dbpA mRNA expression levels were higher in HCC compared to corresponding non-tumor tissues (P<0.01) and higher in non-virus-associated HCC compared to virus-associated cases (P<0.01). dbpA promoter was methylated in 37.7% of HCC samples and the promoter methylation was significantly correlated with the low expression of dbpA in non-virus-associated HCC (P<0.01), but not in virus-associated HCC. Surprisingly, poor prognosis was more significantly associated with high dbpA expression in non-tumorous liver (P=0.018) but not with that in HCC. Non-tumorous tissues consist of chronic hepatitis or liver cirrhosis, and these conditions are the background of hepatocarcinogenesis, defined as the hypercarcinogenic state. Our results suggest that the high expression of dbpA in the hypercarcinogenic state is an indicator of poor prognosis.
AB - We investigated the expression and promoter methylation of dbpA in human hepatocellular carcinoma (HCC) and examined their correlation with clinicophathological features. In 96 paired samples of HCC and adjacent non-tumorous liver, and 10 normal liver specimens, dbpA mRNA was quantified by real-time RT-PCR, and promoter methylation was examined by methylation-specific polymerase chain reaction and bisulfite sequencing. The results showed that dbpA mRNA expression levels were higher in HCC compared to corresponding non-tumor tissues (P<0.01) and higher in non-virus-associated HCC compared to virus-associated cases (P<0.01). dbpA promoter was methylated in 37.7% of HCC samples and the promoter methylation was significantly correlated with the low expression of dbpA in non-virus-associated HCC (P<0.01), but not in virus-associated HCC. Surprisingly, poor prognosis was more significantly associated with high dbpA expression in non-tumorous liver (P=0.018) but not with that in HCC. Non-tumorous tissues consist of chronic hepatitis or liver cirrhosis, and these conditions are the background of hepatocarcinogenesis, defined as the hypercarcinogenic state. Our results suggest that the high expression of dbpA in the hypercarcinogenic state is an indicator of poor prognosis.
KW - DNA binding protein A
KW - Hepatocellular carcinoma
KW - Prognosis
KW - Promoter methylation
UR - http://www.scopus.com/inward/record.url?scp=84857159799&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84857159799&partnerID=8YFLogxK
U2 - 10.3892/ijo.2011.1282
DO - 10.3892/ijo.2011.1282
M3 - Article
C2 - 22159460
AN - SCOPUS:84857159799
SN - 1019-6439
VL - 40
SP - 789
EP - 797
JO - International Journal of Oncology
JF - International Journal of Oncology
IS - 3
ER -