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由Ras和Raf对ERK丝裂原活化蛋白激酶级联反应的调控。

Control of the ERK MAP kinase cascade by Ras and Raf.

作者信息

Marais R, Marshall C J

机构信息

CRC Centre for Cell and Molecular Biology, Institute of Cancer Research, London.

出版信息

Cancer Surv. 1996;27:101-25.

PMID:8909797
Abstract

Activation of ERKs plays a central part in the control of cell proliferation. In this chapter, we have concentrated on the identification and regulation of the kinases that activate Mek. We have chosen to focus on this area because of the many puzzles associated with it. Key issues for the future are the need to derive methods to determine what contribution each individual activator makes to both the magnitude and duration of Mek activation and understanding the mechanisms of regulation. Furthermore, we have considered the roles of Raf and the other kinases solely as Mek activators; they may well have other substrates including cdc25A (Galaktionov et al, 1995), I kappa B (Li and Sedivy, 1993) and TP53 (Jamal and Ziff, 1995).

摘要

细胞外信号调节激酶(ERK)的激活在细胞增殖控制中起着核心作用。在本章中,我们集中探讨了激活丝裂原活化蛋白激酶激酶(Mek)的激酶的鉴定与调控。我们之所以选择聚焦于这一领域,是因为与之相关的诸多谜题。未来的关键问题在于需要找到方法来确定每种单独的激活剂对Mek激活的幅度和持续时间有何贡献,以及理解调控机制。此外,我们仅将Raf和其他激酶视为Mek的激活剂;它们很可能还有其他底物,包括细胞分裂周期蛋白25A(Galaktionov等人,1995年)、核因子κB抑制蛋白(Li和Sedivy,1993年)以及肿瘤蛋白p53(Jamal和Ziff,1995年)。

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