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p53介导密度依赖性生长停滞。

p53 mediates density-dependent growth arrest.

作者信息

Meerson A, Milyavsky M, Rotter V

机构信息

Department of Biological Chemistry, The Alexander Silberman Institute of Life Sciences, Hebrew University, Givat Ram, Jerusalem 91904, Israel.

出版信息

FEBS Lett. 2004 Feb 13;559(1-3):152-8. doi: 10.1016/S0014-5793(04)00027-4.

Abstract

While the stress-response-associated importance of the p53 tumor suppressor is well established, recent studies have also linked p53 with several basic parameters in the normal behavior of cells. Here, we present evidence that basal p53 expression in WI38 human embryonic lung fibroblasts restricts growth rate and mediates density-dependent inhibition of growth and the associated G1 phase arrest of the cell cycle by affecting the density-dependent regulation of p16/INK4a. Additionally, we show that prolonged culturing of hTert-immortalized WI38 cells leads to a loss of density-dependent growth inhibition that correlates with p27/KIP deregulation as well as the previously shown INK4a locus silencing, and to an onset of contact-induced, p53-dependent cell death.

摘要

虽然p53肿瘤抑制因子与应激反应相关的重要性已得到充分证实,但最近的研究也将p53与细胞正常行为中的几个基本参数联系起来。在此,我们提供证据表明,WI38人胚肺成纤维细胞中的基础p53表达通过影响p16/INK4a的密度依赖性调节来限制生长速率,并介导生长的密度依赖性抑制以及细胞周期相关的G1期阻滞。此外,我们表明,hTert永生化WI38细胞的长期培养导致密度依赖性生长抑制丧失,这与p27/KIP失调以及先前所示的INK4a基因座沉默相关,并导致接触诱导的、p53依赖性细胞死亡的发生。

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