Takashima Motonari, Kuramitsu Yasuhiro, Yokoyama Yuichiro, Iizuka Norio, Fujimoto Masanori, Nishisaka Takashi, Okita Kiwamu, Oka Masaaki, Nakamura Kazuyuki
Department of Surgery II, Yamaguchi University School of Medicine, Ube, Japan.
Proteomics. 2005 Apr;5(6):1686-92. doi: 10.1002/pmic.200401022.
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.
为了鉴定可作为丙型肝炎病毒相关肝细胞癌(HCV相关HCC)诊断和治疗分子靶点的蛋白质,我们采用蛋白质组学方法分析人肝脏样本中的蛋白质表达。通过二维凝胶电泳和液相色谱-串联质谱法对26对来自HCV相关HCC患者的肿瘤及相应非肿瘤肝脏样本和6份正常肝脏样本进行了分析。在肿瘤样本中强度高于非肿瘤样本的众多斑点之一被鉴定为α烯醇化酶,它是糖酵解途径中的关键酶。该蛋白的表达随肿瘤去分化而增加,在低分化HCC中显著高于高分化HCC。免疫印迹分析和免疫组织化学重现了这一模式。α烯醇化酶的表达也与肿瘤大小和静脉侵犯呈正相关。这些结果表明,α烯醇化酶是肿瘤进展生物标志物的候选者之一,值得在HCV相关HCC中进一步研究。