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原代及永生化鼻咽上皮细胞中p63表达的调控

Regulation of p63 expression in primary and immortalized nasopharyngeal epithelial cells.

作者信息

Yip Y L, Tsao S W

机构信息

Cancer Biology Laboratory, Department of Anatomy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR, P.R. China.

出版信息

Int J Oncol. 2008 Oct;33(4):713-24. doi: 10.3892/ijo_00000057.

Abstract

Mutation of the p53 gene is a common event in human cancer. Interestingly, p53 mutation is uncommon in nasopharyngeal carcinoma (NPC). The DeltaNp63 has been postulated to have a dominant-negative effect on the function of the p53 gene and may play a role in the pathogenesis of nasopharyngeal carcinoma. Immortalization is a common property of cancer cells and is believed to be an early event in carcinogenesis. At present, the relationship between DeltaNp63 and immortalization is poorly understood. In this study, we defined the expression profile of p63 and its various isoforms in primary and immortalized nasopharyngeal epithelial cells. Also, we elucidated some events regulating the expression of p63. Elevated expression of p63 was generally detected in both primary and immortalized nasopharyngeal epithelial cells at their proliferation stage and the predominant isoform of p63 expressed was DeltaNp63alpha. p63 expression was suppressed upon cellular senescence of primary nasopharyngeal epithelial cells and induction of terminal differentiation in immortalized nasopharyngeal epithelial cells. Expression of DeltaNp63 alone was able to drive clonal proliferation in primary nasopharyngeal cells in culture while downregulation of DeltaNp63 induced cellular apoptosis. All these results support a role of DeltaNp63 in proliferation and immortalization which facilitates pathogenesis of nasopharyngeal carcinoma. TGFbeta and retinoic acid downregulated the expression of p63 in immortalized nasopharyngeal epithelial cells and may play a role in regulating differentiation in squamous epithelial cells with potential applications in prevention and treatment of nasopharyngeal carcinoma.

摘要

p53基因的突变在人类癌症中是常见事件。有趣的是,p53突变在鼻咽癌(NPC)中并不常见。据推测,DeltaNp63对p53基因的功能具有显性负效应,可能在鼻咽癌的发病机制中起作用。永生化是癌细胞的一个共同特性,被认为是致癌过程中的早期事件。目前,DeltaNp63与永生化之间的关系尚不清楚。在本研究中,我们确定了p63及其各种异构体在原代和永生化鼻咽上皮细胞中的表达谱。此外,我们阐明了一些调节p63表达的事件。在原代和永生化鼻咽上皮细胞的增殖阶段通常都检测到p63表达升高,且所表达的p63的主要异构体是DeltaNp63alpha。原代鼻咽上皮细胞发生细胞衰老以及永生化鼻咽上皮细胞诱导终末分化时,p63表达受到抑制。单独DeltaNp63的表达能够驱动培养的原代鼻咽细胞的克隆增殖,而DeltaNp63的下调则诱导细胞凋亡。所有这些结果都支持DeltaNp63在增殖和永生化中发挥作用,这促进了鼻咽癌的发病机制。转化生长因子β(TGFbeta)和视黄酸下调永生化鼻咽上皮细胞中p63的表达,可能在调节鳞状上皮细胞分化中起作用,在鼻咽癌的预防和治疗中具有潜在应用价值。

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