Up-regulation of annexin A2 in cholangiocarcinoma caused by Opisthorchis viverrini and its implication as a prognostic marker

被引:38
作者
Yonglitthipagon, Ponlapat [1 ]
Pairojkul, Chawalit [1 ,2 ]
Chamgramol, Yaovalux [1 ,2 ]
Mulvenna, Jason [4 ]
Sripa, Banchob [1 ,2 ,3 ]
机构
[1] Khon Kaen Univ, Dept Pathol, Fac Med, Khon Kaen 40002, Thailand
[2] Khon Kaen Univ, Fac Med, LFCRC, Khon Kaen 40002, Thailand
[3] Khon Kaen Univ, Trop Dis Res Lab, Khon Kaen 40002, Thailand
[4] James Cook Univ, Cairns, Qld 4870, Australia
关键词
Opisthorchis viverrini; Annexin; ANXA2; Cholangiocarcinoma; Proteomics; Prognotic marker; HEPATOCELLULAR-CARCINOMA; CELL-SURFACE; CANCER CELLS; PROTEOMIC ANALYSIS; II OVEREXPRESSION; PROSTATE-CANCER; EXPRESSION; THAILAND; TUMOR; PHOSPHORYLATION;
D O I
10.1016/j.ijpara.2010.05.002
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Cholangiocarcinoma (CCA), or cancer of the bile ducts, is primarily associated with infection with the liver fluke Opisthorchis viverrini in northeast Thailand. The disease is associated with late presentation, poses challenges for diagnosis and has a high mortality rate - features that highlight the need for tumor markers. At present, there are no specific tumor markers that can indicate the early stages and status of CCA. Proteomic analysis of the proteins expressed on the surface of tumor cells is particularly difficult since proteome-wide analysis of surface membrane proteins has thus far been hampered by the lack of effective strategies to profile hydrophobic membrane proteins. In this study, a sequential protein extraction was utilized to overcome this problem. Membrane protein was extracted from four CCA cell lines with different tumor forming capabilities. The non-tumor H69 biliary cell line was used as a control. Two-dimensional-PAGE followed by MALDI-TOF-MS was used to identify differentially expressed proteins. Among 20 up-regulated membrane proteins identified in the CCA cell lines was ANXA2, a participant in tumor invasion and metastasis in other cancers. Accordingly. ANXA2 was verified in human subjects by probing, using a commercial anti-mouse monoclonal antibody and a tissue microarray of CCA (301 diagnosed cases), where it was found to associate with one of several tumor progression stages as reflected by lymphatic invasion (P = 0.014) and metastasis (P = 0.026). Patients with high expression of ANXA2 had a significantly shorter survival time (P = 0.011). ANXA2 expression in tumors may be useful for predicting the poor outcome of CCA patients. (C) 2010 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1203 / 1212
页数:10
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