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核糖体蛋白S6激酶对核糖体生物合成和功能的协同调节,mTOR功能的关键介质。

Coordinate regulation of ribosome biogenesis and function by the ribosomal protein S6 kinase, a key mediator of mTOR function.

作者信息

Jastrzebski Katarzyna, Hannan Katherine M, Tchoubrieva Elissaveta B, Hannan Ross D, Pearson Richard B

机构信息

Growth Control and Differentiation Program, Trescowthick Research Laboratories, Peter MacCallum Cancer Centre, Melbourne, Australia.

出版信息

Growth Factors. 2007 Aug;25(4):209-26. doi: 10.1080/08977190701779101.

Abstract

Current understanding of the mechanisms by which cell growth is regulated lags significantly behind our knowledge of the complex processes controlling cell cycle progression. Recent studies suggest that the mammalian target of rapamycin (mTOR) pathway is a key regulator of cell growth via the regulation of protein synthesis. The key mTOR effectors of cell growth are eukaryotic initiation factor 4E-binding protein 1 (4EBP-1) and the ribosomal protein S6 kinase (S6K). Here we will review the current models for mTOR dependent regulation of ribosome function and biogenesis as well as its role in coordinating growth factor and nutrient signaling to facilitate homeostasis of cell growth and proliferation. We will place particular emphasis on the role of S6K1 signaling and will highlight the points of cross talk with other key growth control pathways. Finally, we will discuss the impact of S6K signaling and the consequent feedback regulation of the PI3K/Akt pathway on disease processes including cancer.

摘要

目前对细胞生长调控机制的理解,与我们对控制细胞周期进程的复杂过程的了解相比,仍存在显著差距。最近的研究表明,雷帕霉素哺乳动物靶标(mTOR)通路是通过调节蛋白质合成来调控细胞生长的关键因子。细胞生长的关键mTOR效应分子是真核起始因子4E结合蛋白1(4EBP-1)和核糖体蛋白S6激酶(S6K)。在此,我们将综述当前关于mTOR依赖性核糖体功能和生物发生调控的模型,以及其在协调生长因子和营养信号以促进细胞生长和增殖稳态中的作用。我们将特别强调S6K1信号的作用,并突出其与其他关键生长控制通路的相互作用点。最后,我们将讨论S6K信号以及PI3K/Akt通路随之而来的反馈调节对包括癌症在内的疾病进程的影响。

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