TY - JOUR
T1 - Clinical utility of serum fucosylated hemopexin in Japanese patients with hepatocellular carcinoma
AU - Kobayashi, Sayo
AU - Nouso, Kazuhiro
AU - Kinugasa, Hideaki
AU - Takeuchi, Yasuto
AU - Tomoda, Takeshi
AU - Miyahara, Koji
AU - Hagihara, Hiroaki
AU - Kuwaki, Kenji
AU - Onishi, Hideki
AU - Nakamura, Shinichiro
AU - Ikeda, Fusao
AU - Miyake, Yasuhiro
AU - Shiraha, Hidenori
AU - Takaki, Akinobu
AU - Yamamoto, Kazuhide
PY - 2012/12
Y1 - 2012/12
N2 - Aim: Hepatocellular carcinoma (HCC) is a common clinical problem all over the world. Fucosylated hemopexin (Fuc-Hpx) is a newly reported glycoprotein for the diagnosis of HCC, however, its clinical implications are unclear. The aim of this study was to elucidate the clinical utility of Fuc-Hpx in Japanese patients with HCC. Methods: The sera from 331 HCC patients, 45 with liver cirrhosis (LC), 85 with chronic hepatitis (CH) and 22 healthy people were examined for the expression of Fuc-Hpx; the level was compared with clinical parameters as well as hemopexin (Hpx) expression. The expressions of Fuc-Hpx in 12 HCC tissues and corresponding adjacent non-cancerous liver tissues were also examined. Results: No correlation was observed between Hpx and Fuc-Hpx level. The median Fuc-Hpx levels in healthy people and CH, LC and HCC patients were 3.8, 3.7, 6.1 and 7.6AU/mL, respectively (CH vs LC, P=0.002; CH vs HCC, P<0.001; LC vs HCC, P=0.02). Multivariate analysis revealed that low albumin, low prothrombin time and the presence of HCC were significantly correlated with high Fuc-Hpx (P=0.013, =0.001 and <0.001, respectively). Among the HCC patients, albumin was correlated with high Fuc-Hpx; however, none of the tumor factors, such as tumor size, tumor number and tumor stage, was correlated with Fuc-Hpx level. The expression of Fuc-Hpx in cancer tissue was not different from that in non-cancerous tissue. Conclusion: Fuc-Hpx is a valuable biomarker for HCC but it might be a marker for hypercarcinogenic liver rather than a marker for tumor-bearing liver.
AB - Aim: Hepatocellular carcinoma (HCC) is a common clinical problem all over the world. Fucosylated hemopexin (Fuc-Hpx) is a newly reported glycoprotein for the diagnosis of HCC, however, its clinical implications are unclear. The aim of this study was to elucidate the clinical utility of Fuc-Hpx in Japanese patients with HCC. Methods: The sera from 331 HCC patients, 45 with liver cirrhosis (LC), 85 with chronic hepatitis (CH) and 22 healthy people were examined for the expression of Fuc-Hpx; the level was compared with clinical parameters as well as hemopexin (Hpx) expression. The expressions of Fuc-Hpx in 12 HCC tissues and corresponding adjacent non-cancerous liver tissues were also examined. Results: No correlation was observed between Hpx and Fuc-Hpx level. The median Fuc-Hpx levels in healthy people and CH, LC and HCC patients were 3.8, 3.7, 6.1 and 7.6AU/mL, respectively (CH vs LC, P=0.002; CH vs HCC, P<0.001; LC vs HCC, P=0.02). Multivariate analysis revealed that low albumin, low prothrombin time and the presence of HCC were significantly correlated with high Fuc-Hpx (P=0.013, =0.001 and <0.001, respectively). Among the HCC patients, albumin was correlated with high Fuc-Hpx; however, none of the tumor factors, such as tumor size, tumor number and tumor stage, was correlated with Fuc-Hpx level. The expression of Fuc-Hpx in cancer tissue was not different from that in non-cancerous tissue. Conclusion: Fuc-Hpx is a valuable biomarker for HCC but it might be a marker for hypercarcinogenic liver rather than a marker for tumor-bearing liver.
KW - Biomarker
KW - Fucosylated hemopexin
KW - Glycosylation
KW - Hepatocellular carcinoma
KW - Hypercarcinogenicity
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U2 - 10.1111/j.1872-034X.2012.01044.x
DO - 10.1111/j.1872-034X.2012.01044.x
M3 - Article
C2 - 22639859
AN - SCOPUS:84870257371
SN - 1386-6346
VL - 42
SP - 1187
EP - 1195
JO - Hepatology Research
JF - Hepatology Research
IS - 12
ER -