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在一种人类鼻咽癌细胞系中,δNp63的过表达会下调细胞周期蛋白依赖性激酶抑制因子(CKIs)并增强细胞增殖。

Overexpression of delta Np63 in a human nasopharyngeal carcinoma cell line downregulates CKIs and enhances cell proliferation.

作者信息

Chiang Chi-Tai, Chu Wing-Keung, Chow Shu-Er, Chen Jan-Kan

机构信息

Department of Physiology, College of Medicine, Chang Gung University, Taoyuan, Taiwan.

出版信息

J Cell Physiol. 2009 Apr;219(1):117-22. doi: 10.1002/jcp.21656.

Abstract

p63 belongs to a member of the tumor suppressor protein p53 family. Due to alternative promoter usage, two types of p63 proteins are produced. The DeltaNp63 isoform lacks the N-terminal transactivation domain and is thought to antagonize TAp63 and p53 in target gene regulation. DeltaNp63 has been found to be overexpressed in numerous human squamous cell carcinomas, including nasopharyngeal carcinoma (NPC). However, the role of DeltaNp63 overexpression in NPC pathogenesis has not been clear. In this study, we use a DeltaNp63 overexpressing human NPC cell line (NPC-076) to explore the possible roles of DeltaNp63 in cell proliferation and cell-cycle regulation. We found that the proliferation of NPC-076 cell is greatly suppressed when the overexpressed DeltaNp63 is silenced by specific DeltaNp63 siRNA. Further studies show that DeltaNp63 silencing results in the upregulation of CKIs, including p27(kip1) and p57(kip2) in both mRNA and protein levels. Cell-cycle analysis shows that DeltaNp63 silencing also results in an increased G1 phase cell and apoptotic cell population. Our findings indicate that DeltaNp63 plays important roles in the regulation of NPC-076 cell-cycle progression, and may play a role in the maintenance of NPC-076 tumor cell phenotype.

摘要

p63属于肿瘤抑制蛋白p53家族的一员。由于启动子使用方式的不同,会产生两种类型的p63蛋白。DeltaNp63亚型缺乏N端反式激活结构域,被认为在靶基因调控中拮抗TAp63和p53。已发现DeltaNp63在包括鼻咽癌(NPC)在内的多种人类鳞状细胞癌中过表达。然而,DeltaNp63过表达在NPC发病机制中的作用尚不清楚。在本研究中,我们使用过表达DeltaNp63的人类NPC细胞系(NPC-076)来探讨DeltaNp63在细胞增殖和细胞周期调控中的可能作用。我们发现,当通过特异性DeltaNp63 siRNA使过表达的DeltaNp63沉默时,NPC-076细胞的增殖受到极大抑制。进一步研究表明,DeltaNp63沉默导致细胞周期蛋白依赖性激酶抑制剂(CKIs)上调,包括p27(kip1)和p57(kip2)的mRNA和蛋白水平均上调。细胞周期分析表明,DeltaNp63沉默还导致G1期细胞和凋亡细胞数量增加。我们的研究结果表明,DeltaNp63在NPC-076细胞周期进程的调控中起重要作用,并且可能在维持NPC-076肿瘤细胞表型中发挥作用。

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