Ding Shi-Jian, Li Yan, Tan Ye-Xiong, Jiang Man-Rong, Tian Bo, Liu Ying-Kun, Shao Xiao-Xia, Ye Sheng-Long, Wu Jia-Rui, Zeng Rong, Wang Hong-Yang, Tang Zhao-You, Xia Qi-Chang
Research Center for Proteome Analysis, Key Laboratory of Proteomics, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, CAS, Shanghai 200031, People's Republic of China.
Mol Cell Proteomics. 2004 Jan;3(1):73-81. doi: 10.1074/mcp.M300094-MCP200. Epub 2003 Oct 30.
To better understand the mechanism underlying the hepatocellular carcinoma (HCC) metastasis and to search potential markers for HCC prognosis, differential proteomic analysis on two well-established HCC cell strains with high and low metastatic potentials, MHCC97-H and MHCC97-L, was conducted using two-dimensional gel electrophoresis followed by matrix-assisted laser desorption/time-of-flight mass spectrometry. Cytokeratin 19 (CK19) was identified and found to be overexpressed in MHCC97-H as compared with MHCC97-L. This result was further confirmed by two-dimensional Western blot analysis and immunofluorescence assay. Furthermore, one-dimensional Western blot analysis showed consistently increased CK19 expression in progressively more metastatic cells. Immunohistochemical study on 102 human HCC specimens revealed that more patients in the CK19-positive group had overt intrahepatic metastases (satellite nodules, p < 0.05; vascular tumor emboli, p < 0.001; tumor node metastatis staging, p < 0.001). CK19 fragment CYFRA 21-1 levels measured in sera from nude mice model of human HCC metastasis with radioimmunoassay increased in parallel with tumor progression and rose remarkably when pulmonary metastases occurred. The results demonstrated that overexpression of CK19 in HCC cells is related to metastatic behavior. Serum CK19 level might reflect the pathological progression in some HCC and may be a useful marker for predicting tumor metastasis and a therapeutic target for the treatment of HCC patients with metastases.
为了更好地理解肝细胞癌(HCC)转移的潜在机制,并寻找HCC预后的潜在标志物,我们采用二维凝胶电泳结合基质辅助激光解吸/飞行时间质谱技术,对两种具有高转移潜能和低转移潜能的成熟HCC细胞株MHCC97-H和MHCC97-L进行了差异蛋白质组学分析。细胞角蛋白19(CK19)被鉴定出来,并且发现与MHCC97-L相比,其在MHCC97-H中过表达。二维蛋白质印迹分析和免疫荧光测定进一步证实了这一结果。此外,一维蛋白质印迹分析显示,在转移性逐渐增加的细胞中,CK19表达持续增加。对102例人类HCC标本进行的免疫组织化学研究表明,CK19阳性组中更多患者出现明显的肝内转移(卫星结节,p<0.05;血管肿瘤栓子,p<0.001;肿瘤淋巴结转移分期,p<0.001)。通过放射免疫测定法检测人HCC转移裸鼠模型血清中的CK19片段CYFRA 21-1水平,其随肿瘤进展而平行升高,当发生肺转移时显著升高。结果表明,HCC细胞中CK19的过表达与转移行为有关。血清CK19水平可能反映某些HCC的病理进展,可能是预测肿瘤转移的有用标志物以及治疗有转移的HCC患者的治疗靶点。