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作 者:张婷婷[1] 倪润洲[1] 倪温慨[1] 刘肇修[1] 管程齐[1] 朱隽雅[1] 王靓[1] 王亚运[1] 仇惠元
出 处:《交通医学》2016年第3期205-208,共4页Medical Journal of Communications
基 金:国家自然科学基金面上项目(81472272);国家自然科学基金青年项目(81502070);南通大学研究生科技创新计划项目(YKS14013)
摘 要:目的:探讨Prdx1、Spy1、p27^(kip1)蛋白在肝细胞肝癌中的表达及相关性。方法:应用Western blot及免疫组化检测肝癌及相应的癌旁组织中Prdx1、Spy1、p27^(kip1)的表达;免疫共沉淀分析Prdx1、Spy1的相互作用;Western blot分析Prdx1、Spy1相互结合对p27^(kip1)蛋白表达的影响。结果:Prdx1、Spy1在肝癌组织及肝癌细胞中高表达,与p27^(kip1)表达呈负相关;Prdx1、Spy1相互结合使p27^(kip1)的表达水平下调,此作用与Prdx1的抗氧化物活性无关。结论:Prdx1、Spy1蛋白的表达与肝细胞肝癌的发生发展有关,两者的表达可能在肿瘤的恶性进展中起协同作用,而与p27^(kip1)的表达呈拮抗作用。Objectiv e:To investigate the expressions and correlation between Prdx1, Spy1 and p27^kip1 proteins in hepatocellular carcinoma. Methods: Western blot and Immunohistochemical analysis were used to examine the expression of Prdx1, Spy1 and p27^kip1; immunoprecipitation assay was used to identify Prdx1 as a novel binding partner for Spy1. Results: Prdx1 and Spy1 expressions were observed in normal liver tissues distant from the tumors. It was also observed that partial co-localization of Prdx1 and Spy1 in HCC and Prdx1 interacted with Spy1 in liver tissue and HCC cells indicating that Prdx1 could potentially influence p27^kip1 function via Spy1. It was also showed that the antioxidant activity of Prdx1 was not essential for the formation of Prdx1/Spy1 complex. Conclusions: The abnormal expression of Prdx1 and Spy1 play possibly the promoting roles in HCC. The Prdx1 expression was significantly increased in HCC accompanying an increase in Spy1 levels and a decrease in p27^kip1 levels.
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