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作 者:李拥军[1] 张卫华[1] 沈彪[1] 杨书云[1] 沈爱国[1]
出 处:《现代肿瘤医学》2013年第12期2762-2764,共3页Journal of Modern Oncology
摘 要:目的:研究MIF4GD(middle domain of eukaryotic initiation factor 4G)在肝细胞肝癌(hepatocellular carcinoma,HCC)组织中的表达及临床意义。方法:免疫组织化学方法检测108例HCC石蜡切片中MIF4GD的表达。Kaplan-Meier生存曲线分析患者的生存率,COX模型多因素分析MIF4GD的表达与患者临床预后的相关性。结果:免疫组化结果显示MIF4GD在高分化的癌组织中表达较高,MIF4GD表达与组织分化程度、是否伴有肝硬化和有无静脉侵袭相关,差异有统计学意义(P<0.05)。生存分析表明MIF4GD高表达的患者预后良好(P<0.05)。COX模型多因素分析显示MIF4GD可以作为患者独立的预后指标(P<0.05)。结论:MIF4GD在HCC中表达下调,可能成为肝癌治疗的新靶点。Objective:To investigate the expression and significance of Middle domain of eukaryotic initiation fac- tor 4G (MIF4GD) in hepatocellular carcinoma (HCC) tissues. Methods: Immunohistochemical analysis was used to detect the expression of MIF4GD in 108 HCC samples. Survival curve was calculated using the Kaplan - meier meth- od, and the prognosis was analyzed with multivariate COX proportional hazards regression analysis. Results:Immuno- histochemistry showed that the expression of MIF4GD was higher in well differentiated tissues. And MIF4GD expres- sion was correlated with differentiation degree, cirrhosis, and vein invasion ( P 〈 0.05 ). The Kaplan - Meier survival curve showed that high MIF4GD expression was related to a well survival with statistical significance( P 〈 0.05 ). Mul- tivariate COX proportional hazards regression analysis indicated that MIF4GD expression was an independent prognos- tic marker for HCC (P 〈 0.05 ). Conclusion:The expression of MIF4GD was downregulated significantly in HCC tis- sues, and provided a new target for therapy of HCC.
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