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CREB——肿瘤发生中的真正罪魁祸首。

CREB--a real culprit in oncogenesis.

作者信息

Siu Yeung-Tung, Jin Dong-Yan

机构信息

Department of Biochemistry, The University of Hong Kong, Hong Kong, China.

出版信息

FEBS J. 2007 Jul;274(13):3224-32. doi: 10.1111/j.1742-4658.2007.05884.x. Epub 2007 Jun 12.

Abstract

The cAMP response element-binding protein (CREB) is a stimulus-induced transcription factor that responds rapidly to phosphorylation and/or coactivator activation. Regulated activation of CREB has a significant impact on cellular growth, proliferation and survival. To overturn the cellular control of these processes, tumor cells have developed various mechanisms to achieve constitutive activation of CREB, including gene amplification, chromosome translocation, interaction with viral oncoproteins, and inactivation of tumor suppressor genes. These mechanisms converge on the phosphorylation of CREB and/or the activation of transducer of regulated CREB activity (TORC) coactivators to effect uncontrolled proliferation of cells. This minireview summarizes the different lines of existing evidence that support a direct role of CREB in oncogenesis.

摘要

环磷酸腺苷反应元件结合蛋白(CREB)是一种受刺激诱导的转录因子,对磷酸化和/或共激活因子激活反应迅速。CREB的调控激活对细胞生长、增殖和存活有重大影响。为了颠覆这些过程的细胞控制,肿瘤细胞已发展出各种机制来实现CREB的组成型激活,包括基因扩增、染色体易位、与病毒癌蛋白相互作用以及肿瘤抑制基因失活。这些机制都集中在CREB的磷酸化和/或调节CREB活性的转导子(TORC)共激活因子的激活上,以实现细胞的不受控制增殖。本综述总结了支持CREB在肿瘤发生中直接作用的不同现有证据。

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