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

机译:核糖体蛋白S6激酶(mTOR功能的关键介体)对核糖体生物发生和功能的协调调节。

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摘要

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.
机译:当前对调节细胞生长的机制的了解大大落后于我们对控制细胞周期进程的复杂过程的了解。最近的研究表明,雷帕霉素(mTOR)途径的哺乳动物靶标是通过调节蛋白质合成来调节细胞生长的关键调节剂。细胞生长的关键mTOR效应子是真核起始因子4E结合蛋白1(4EBP-1)和核糖体蛋白S6激酶(S6K)。在这里,我们将回顾mTOR依赖核糖体功能和生物发生的调控的当前模型,以及其在协调生长因子和营养信号传导中促进细胞生长和增殖动态平衡的作用。我们将特别强调S6K1信号传导的作用,并强调与其他关键生长控制途径的串扰点。最后,我们将讨论S6K信号传导的影响以及PI3K / Akt信号通路对包括癌症在内的疾病过程的反馈调节。

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