Overexpression of alpha enolase in hepatitis C virus-related hepatocellular carcinoma: Association with tumor progression as determinedby proteomic analysis

被引:126
作者
Takashima, M
Kuramitsu, Y
Yokoyama, Y
Iizuka, N
Fujimoto, M
Nishisaka, T
Okita, K
Oka, M
Nakamura, K
机构
[1] Yamaguchi Univ, Sch Med, Dept Biochem & Biomol Recognit, Ube, Yamaguchi 7558505, Japan
[2] Yamaguchi Univ, Sch Med, Dept Surg 2, Ube, Yamaguchi 7558505, Japan
[3] Yamaguchi Univ, Sch Med, Dept Gastroenterol & Hepatol, Ube, Yamaguchi 7558505, Japan
[4] Yamaguchi Univ, Sch Med, Dept Bioregulatory Funct, Ube, Yamaguchi 7558505, Japan
[5] Hiroshima Prefectural Hosp, Dept Pathol, Hiroshima, Japan
关键词
alpha enolase; hepatitis C virus; hepatocellular carcinoma;
D O I
10.1002/pmic.200401022
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
To identify proteins that could be molecular targets for diagnosis and treatment of hepatitis C virus-related hepatocellular carcinoma (HCV-related HCC), we used a proteomic approach to analyze protein expression in samples of human liver. Twenty-six pairs of tumorous and corresponding nontumorous liver samples from patients with HCV-related HCC and six normal liver samples were analyzed by two-dimensional gel electrophoresis and liquid chromatography-tandem mass spectrometry. One of the numerous spots that showed stronger intensity in tumorous than in nontumorous samples was identified as alpha enolase, a key enzyme in the glycolytic pathway. Expression of this protein increased with tumor dedifferentiation and was significantly higher in poorly differentiated HCC than in well-differentiated HCC. This pattern was reproduced by immunoblot analysis and immunohistochemistry. Expression of alpha enolase also correlated positively with tumor size and venous invasion. These results suggest that alpha enolase is one of the candidates for biomarkers for tumor progression that deserves further investigation in HCV-related HCC.
引用
收藏
页码:1686 / 1692
页数:7
相关论文
共 29 条
[1]   NONNEURONAL ENOLASE IS AN ENDOTHELIAL HYPOXIC STRESS PROTEIN [J].
AARONSON, RM ;
GRAVEN, KK ;
TUCCI, M ;
MCDONALD, RJ ;
FARBER, HW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (46) :27752-27757
[2]   Two-dimensional gel analysis of human endometrial proteins: characterization of proteins with increased expression in hyperplasia and adenocarcinoma [J].
Byrjalsen, I ;
Larsen, PM ;
Fey, SJ ;
Nilas, L ;
Larsen, MR ;
Christiansen, C .
MOLECULAR HUMAN REPRODUCTION, 1999, 5 (08) :748-756
[3]   Proteomic identification of oxidatively modified proteins in Alzheimer's disease brain.: Part II:: dihydropyrimidinase-related protein 2, α-enolase and heat shock cognate 71 [J].
Castegna, A ;
Aksenov, M ;
Thongboonkerd, V ;
Klein, JB ;
Pierce, WM ;
Booze, R ;
Markesbery, WR ;
Butterfield, DA .
JOURNAL OF NEUROCHEMISTRY, 2002, 82 (06) :1524-1532
[4]  
Chang YS, 2003, CLIN CANCER RES, V9, P3641
[5]  
Durany N, 2000, BRIT J CANCER, V82, P20
[6]   Rising incidence of hepatocellular carcinoma in the United States [J].
El-Serag, HB ;
Mason, AC .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (10) :745-750
[7]   Proteome analysis of human liver tumor tissue by two-dimensional gel electrophoresis and matrix assisted laser desorption/ionization-mass spectrometry for identification of disease-related proteins [J].
Kim, J ;
Kim, SH ;
Lee, SU ;
Ha, GH ;
Kang, DG ;
Ha, NY ;
Ahn, JS ;
Cho, HY ;
Kang, SJ ;
Lee, YJ ;
Hong, SC ;
Ha, WS ;
Bae, JM ;
Lee, CW ;
Kim, JW .
ELECTROPHORESIS, 2002, 23 (24) :4142-4156
[8]  
Kim W, 2003, CLIN CANCER RES, V9, P5493
[9]   Protein profiling and identification of modulators regulated by the E7 oncogene in the C33A cell line by proteomics and genomics [J].
Lee, KA ;
Shim, JH ;
Kho, CW ;
Park, SG ;
Park, BC ;
Kim, JW ;
Lim, JS ;
Choe, YK ;
Paik, SG ;
Yoon, DY .
PROTEOMICS, 2004, 4 (03) :839-848
[10]   Proteome analysis of hepatocellular carcinoma [J].
Lim, SO ;
Park, SJ ;
Kim, W ;
Park, SG ;
Kim, HJ ;
Kim, YI ;
Sohn, TS ;
Noh, JH ;
Jung, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 291 (04) :1031-1037