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Skp2通过抑制p300来抑制p53依赖性凋亡。

Skp2 suppresses p53-dependent apoptosis by inhibiting p300.

作者信息

Kitagawa Mayumi, Lee Sang Hyun, McCormick Frank

机构信息

Cancer Research Institute and Comprehensive Cancer Center, University of California-San Francisco, San Francisco, CA 94115, USA.

出版信息

Mol Cell. 2008 Feb 1;29(2):217-31. doi: 10.1016/j.molcel.2007.11.036.

Abstract

The F box protein Skp2 is oncogenic, and its frequent amplification and overexpression correlate with the grade of malignancy of certain tumors. Conversely, depletion of Skp2 decreases cell growth and increases apoptosis. Here, we show that Skp2 counteracts the transactivation function of p53 and suppresses apoptosis mediated by DNA damage or p53 stabilization. We demonstrate that Skp2 forms a complex with p300 through the CH1 and the CH3 domains of p300 to which p53 is thought to bind and antagonizes the interaction between p300 and p53 in cells and in vitro. As Skp2 antagonizes the interaction between p300 and p53, Skp2 suppresses p300-mediated acetylation of p53 and the transactivation ability of p53. Conversely, ectopic expression of p300 rescues the transactivation function of p53 in cells overexpressing Skp2. Taken together, our results indicate that Skp2 controls p300-p53 signaling pathways in cancer cells, making Skp2 a potential molecular target for cancer therapy.

摘要

F 盒蛋白 Skp2 具有致癌性,其频繁扩增和过表达与某些肿瘤的恶性程度相关。相反,Skp2 的缺失会降低细胞生长并增加细胞凋亡。在此,我们表明 Skp2 可对抗 p53 的反式激活功能,并抑制由 DNA 损伤或 p53 稳定介导的细胞凋亡。我们证明 Skp2 通过 p300 的 CH1 和 CH3 结构域与 p300 形成复合物,而 p53 被认为可结合至该结构域,并且 Skp2 在细胞内和体外均可拮抗 p300 与 p53 之间的相互作用。由于 Skp2 拮抗 p300 与 p53 之间的相互作用,Skp2 可抑制 p300 介导的 p53 乙酰化以及 p53 的反式激活能力。相反,p300 的异位表达可挽救过表达 Skp2 的细胞中 p53 的反式激活功能。综上所述,我们的结果表明 Skp2 可控制癌细胞中的 p300 - p53 信号通路,这使得 Skp2 成为癌症治疗的潜在分子靶点。

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