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机构地区:[1]郧阳医学院附属人民医院消化科,湖北十堰442000 [2]武汉大学中南医院消化科
出 处:《中国肿瘤临床与康复》2006年第6期488-490,共3页Chinese Journal of Clinical Oncology and Rehabilitation
摘 要:目的探讨细胞S相激酶相关蛋白(Skp2)、p27^(kipl)蛋白表达与食管癌的关系。方法用免疫组化S-P法检测58例食管癌中Skp2、p27^(kipl)蛋白的表达。结果58例食管癌组织中Skp2、p27^(kipl)蛋白阳性表达率分别为32.76%和58.62%;二者的阳性表达率均与食管癌患者的年龄、性别、肿瘤部位无关(P>0.05)。Skp2阳性表达率随肿瘤分化程度降低而升高,p27^(kipl)阳性表达率随肿瘤分化程度降低、浸润深度加深、恶性程度增加而逐渐降低(P<0.05)。Skp2与p27^(kipl)表达呈显著负相关(P<0.01)。结论在管癌中Skp2主要的泛素化降解靶物质是p27^(kipl),它通过影响p27^(kipl)降解进而影响肿瘤的进展,导致不良预后。Objective To investigate the clinical significance of p27^kipl and S-phase kinase-associated protein 2 (Skp2) expression in human esophageal squamous cell carcinoma(SCC). Methods The expression of p27^kipl and Skp2 was determined by SP method in 58 specimens of esophageal SCC. Results The positive rates of p27^kipl and Skp2 expression were 32.8% and 58.6%, respectively. The positive rates of both p27^kipland Skp2 expression were not associated with the patients' age, sex and tumor location ( P 〉 0.05). The positive rate of Skp2 expression increased with decreasing differentiation degree of esophageal SCC,while the positive rate of p27^kipl expression in esophageal SCC decreased with the poor differentiation,deep invasion and increase in malignant grade ( P 〈 0.05). There was a negative correlation between the p27^kipl and Skp2 expression(P 〈 0.01 ). Conclusion The target substrate of Skp2 in esophageal SCC is mainly p27^kipl ,and Skp2-indueed degradation of p27^kipl may influence tumor progression and lead to a poor prognosis.
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