摘要
目的:探讨肝细胞癌(HCC)组织中Smac(第二个线粒体Caspase激活因子)的表达及其与细胞凋亡和增殖的关系。方法:应用免疫组化二步法检测HCC及相应癌旁肝硬化组织各41例、肝血管瘤旁正常对照组织9例中Smac、增殖细胞核抗原(PCNA)的表达;应用TUNEL法检测组织中细胞的凋亡。结果:在41例HCC组织中,Smac阳性数为14例(34.14%),相应癌旁肝硬化组织为23例(56.10%),肝血管瘤旁正常对照组织为7例(77.78%),HCC组织中Smac的阳性率与相应癌旁及正常组织相比差异有统计学意义,χ2值分别为3.989和4.115,P值分别为0.046和0.042;HCC组织中Smac蛋白的表达与细胞的凋亡增殖比有相关性,t′=2.26,P<0.05,而与患者的年龄、组织分化程度等临床病理指标均无相关性,P均>0.05。结论:Smac的相对低表达或表达缺失在一定程度上打破了HCC组织中细胞凋亡与增殖之间的动态平衡,在HCC的形成过程中起到了重要的作用。
OBJECTIVE:To investigate the expression of Smac protein in human hepatocelluar carcinoma and their relationship with cell apoptosis and proliferation.METHODS:The expression of Smac and the proliferating cell nuclear antign (PCNA) in 41 cancer tissues,41 adjacent cirrhosis tissues and 9 normal control tissues in hemangioma were assessed by the two-step immunohistochemical method and the apoptosis was detected by the TUNEL method.RESULTS:Smac proteins were expressed in 14(34.14%) of the 41 cases of hepatocelluar carcinoma,in 23(56.10%) of the 41 cases of the adjacent cirrhosis tissues,and in 7(77.78%) of the normal tissues in hemangioma.The smac protein positive expression rate in hepatocelluar carcinoma was significantly higher than that in the adjacent cirrhosis tissues and the normal control tissues,χ^2 values were 3.989 and 4.115,P values were 0.046 and 0.042.The Smac protein expression in cancer was significantly correlated with the ratio of apoptic index to proliferative index (t′=2.26,P〈0.05),but was not with the clinicopathological indicators such as the age and histological grade (P〈0.05).CONCLUSION:The relatively lower level of the expression of Smac may in a certain extent break the dynamic balance between apoptosis and proliferation of hepatocelluar carcinoma cells,then play an important role in the pathogenesis of hepatocelluar carcinoma.
出处
《中华肿瘤防治杂志》
CAS
2010年第8期609-612,共4页
Chinese Journal of Cancer Prevention and Treatment
关键词
癌
肝细胞/病理学
肝肿瘤/病理学
细胞凋亡
细胞增殖
免疫组织化学
carcinoma ,hepatocellular/pathology
liver neoplasms/pathology
apoptosis
proliferation
immunohistochemistry