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p57^(kip2)在肝癌组织中的表达及其与临床病理因素、PCNA和p53的关系 被引量:3

Expression of p57^(kip2) and its relationships with clinicopathology, PCNA and p53 in primary hepatocellular carcinoma
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摘要 目的 :检测细胞周期抑制因子 p5 7kip2 在肝癌中的表达水平 ,探讨它与临床病理因素、增殖细胞核抗原 (PCNA)、p5 3的关系 .方法 :用免疫组织化学法检测 32例肝癌组织和1 0例正常肝脏组织中 p5 7kip2 ,PCNA和 p5 3的表达水平 .结果 :p5 7kip2 在肝癌组织中的阳性率 5 6 .2 % ,显著低于正常肝脏组织 (1 0 0 % ) (P =0 .0 1 1 ) ,p5 7kip2 的缺失表达与肝癌细胞的分化较差 (P =0 .0 0 7)、临床分期较晚 (P =0 .0 4 1 )及预后较差有关 (P =0 .0 36 ) ,与年龄、AFP ,肿瘤大小及肿瘤侵犯转移无显著相关 (P >0 .0 5 ) ;PCNA在肝癌组织中阳性率为 5 6 .2 % ,与 p5 7kip2 的表达有关 (P =0 .0 36 ) ;p5 3在肝癌组织中的阳性率 4 6 .9% ,与p5 7kip2 表达在统计学上无相关性 (P >0 .0 5 ) .结论 :肝癌组织中存在 p5 7kip2 的表达缺失、PCNA的高表达 ,共同参与肝癌的发生、发展 ,而p5 7kip2 和p5 AIM: To investigate the expression of p57 kip2 and its relationship with clinicopathology, PCNA and p53 in primary hepatocellular carcinoma (HCC). METHODS: Expression of p57 kip2 , PCNA and p53 in tumor tissues from 32 patients with HCC and 10 liver tissues of normal persons was detected with Elivision immunohistochemical technique. RESULTS: p57 kip2 protein positive expression rate in HCC was 56.2%,which was lower than that in normal tissues (100%) ( P =0.011). The reduced expression of p57 kip2 protein correlated significantly with moderate or low differentiation of tumor cells ( P =0.007), high clinical stage ( P =0.041) and poor prognosis ( P =0.036), but did not correlate significantly with metastasis, tumor size, level of AFP and age ( P >0.05). PCNA positive expression rate was 56.2%, which was correlated significantly with the expression of p57 kip2 ( P =0.036) and p53 positive expression rate was 46.9%, which was not correlated significantly with the expression of p57 kip2 ( P >0.05). CONCLUSION: There is a marked loss or absence of p57 kip2 expression and high expression of PCNA in HCC, which are involved in the carcinogenesis and development of HCC. p57 kip2 and p53 may induce apoptosis via different mechanisms.
出处 《第四军医大学学报》 CAS 北大核心 2004年第17期1562-1565,共4页 Journal of the Fourth Military Medical University
关键词 p57kip2基因 原发性肝癌 增殖细胞核抗原 P53 p57 kip2 gene HCC PCNA p53
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