机构地区:[1]第三军医大学西南医院全军肝胆外科研究所,重庆400038
出 处:《第三军医大学学报》2014年第10期1068-1073,共6页Journal of Third Military Medical University
摘 要:目的探讨肝癌干细胞表面标志物CD44、CD133与组织因子(tissue factor,TF)在肝癌组织中的表达及分析其与肝癌临床病理资料及生存预后间的相互关系。方法应用免疫组化法检测387例肝癌组织中CD44、CD133和TF的表达,比较其表达与肝癌临床病理资料及预后间的关系。结果①387例肝癌组织中CD44、CD133和TF的阳性率分别为60.47%、55.81%和65.12%;CD44与CD133双阳性表达(CD44+CD133+)阳性率41.60%;CD44、CD133和TF三阳性表达(CD44+CD133+TF+)阳性率35.14%;②CD44、CD133与TF单独阳性表达以及CD44+CD133+和CD44+CD133+TF+均与肝癌患者门静脉癌栓、TNM分期和Edmendson分级具显著相关性(P<0.01);③CD90、CD44和CD133蛋白表达呈正相关(P<0.01);④CD44、CD133和TF阳性组的总生存时间短于阴性组,差异有统计学意义(P<0.05);CD44+CD133+组总生存时间短于非CD44+CD133+组总生存时间及CD44+CD133+TF+组总生存时间短于非CD44+CD133+TF+组,差异均有统计学意义(P<0.01);⑤多因素分析门静脉癌栓、TF+、CD44+CD133+和CD44+CD133+TF+是影响肝癌预后的独立危险因数(P<0.01)。结论 CD44、CD133和TF均与门静脉癌栓形成及恶性预后密切相关,可作为判断患者预后的指标。Objective Investigate the expression of CD44, CD133 and tissue factor (TF) and their clinicopathologic significance in hepatocellular carcinoma (HCC). Methods The expression of CD44, CDI33 and TF was detected using immunohistochemistry in 387 liver tissue samples from HCC patients. We further evaluated the relationship between the expression and clinical pathology and prognosis of HCC. Results The positive expression rates of CD44, CD133 and TF in HCC patients were 60.47%, 55.81%, and 65.12%, respectively. The positive rate of co-expression of CD44 and CD133 (CD44 + CD133 + ) was 41.60%. The pos- itive rate of co-expression of CD44, CD133 and TF (CD44+ CD133+ TF+ ) was 35.14%. Clinical analysis showed that single expression of CD44, CD133 or TF was associated with portal vein tumor thrombus, TNM staging and grading of Edmendson. CD44 + CD133 + and CD44 + CD133 + TF+ had the same results (P 〈0. 01 and P 〈0. 01, respectively). The difference of survival rate between CD44-positive and CD44-negative groups was observed, and the CD133-positive and CD133-negative groups as well as the TF-positive and TF-negative groups had the same result (P 〈 0.01 all). The protein expression CD90, CD44 and CD133 was positively correlated (P 〈0. 01 ). The total survival time of CIM4, CD133 and TF positive groups was shorter than the negative groups and the differences were statistically significant ( all P 〈 0. 01 ). The total survival time of CD44 + CD133 + group was shorter than that of non-CD44 + group (P 〈 0.01 ). The total survival time of CD44 + CD133 + TF+ group was shorter than that of non-CD44 + CD133 + TF + group and the differences were statistically significant ( P 〈 0. 01 ). Multivariate analysis suggested that portal vein tumor thrombus, TF +CI)44 + CD133 + and CD44 + CD133+ TF+ were the independent risk factors of the prognosis of HCC (P 〈0. 01 all). Conclusion The positive expression of CIM4, CD133 and TF is
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