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p53与SV40介导的细胞转化

p53 and transformation by SV40.

作者信息

O'Reilly D R

出版信息

Biol Cell. 1986;57(3):187-96. doi: 10.1111/j.1768-322x.1986.tb00475.x.

Abstract

The large T antigen of SV40 is able to immortalize and transform primary and established cells in culture, and can, at least in certain cases, confer a tumorigenic phenotype on the infected cell. T antigen has been shown to induce cellular DNA synthesis in the infected cell and this activity is likely to be instrumental in T antigen mediated oncogenesis. A property of T antigen which may be of paramount importance to its oncogenic and mitogenic activities is its ability to specifically bind and stabilize the cellular protein p53. p53 has been implicated in the control of the passage of the cell from G0 arrest to G1 and S phase. Furthermore, altered p53 expression is strongly associated with various phenotypes of the transformed state, and p53 has been identified as an immortalizing oncogene. Thus it is possible that p53-fixation by T antigen is responsible for its transforming potential. In this article, the transforming activities of T antigen and p53 are reviewed, and the possible relevance of p53-binding to T antigen-induced transformation is discussed.

摘要

SV40的大T抗原能够使培养中的原代细胞和已建立的细胞永生化并发生转化,并且至少在某些情况下,能赋予被感染细胞致瘤表型。T抗原已被证明能在被感染细胞中诱导细胞DNA合成,这种活性可能在T抗原介导的肿瘤发生中起作用。T抗原的一个对其致癌和促有丝分裂活性可能至关重要的特性是它能够特异性结合并稳定细胞蛋白p53。p53与控制细胞从G0期停滞进入G1期和S期有关。此外,p53表达的改变与转化状态的各种表型密切相关,并且p53已被鉴定为一种永生化癌基因。因此,T抗原对p53的固定作用可能是其转化潜能的原因。在本文中,我们综述了T抗原和p53的转化活性,并讨论了p53结合与T抗原诱导的转化之间可能的相关性。

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