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小GTP酶信号转导通路如何调节细胞周期进入?

How do small GTPase signal transduction pathways regulate cell cycle entry?

作者信息

Marshall C

机构信息

Chester Beatty Laboratories, Cancer Research Campaign Centre for Cell and Molecular Biology, Institute of Cancer Research, London, SW3 6JB, UK.

出版信息

Curr Opin Cell Biol. 1999 Dec;11(6):732-6. doi: 10.1016/s0955-0674(99)00044-7.

DOI:10.1016/s0955-0674(99)00044-7
PMID:10600705
Abstract

A variety of studies have shown that activation of the cell cycle machinery requires the participation of multiple signalling pathways. These pathways include Ras-dependent effectors such as the extracellular-signal related kinases, otherwise known as mitogen-activated protein kinases (ERKs, MAPKs), phosphatidylinositol 3 (PI3)-kinase and p21Ral pathways, as well as other signalling pathways regulated by the small GTPases p21Rho, p21Rac and p21Cdc42.

摘要

各种研究表明,细胞周期机制的激活需要多种信号通路的参与。这些通路包括依赖Ras的效应器,如细胞外信号相关激酶,也称为丝裂原活化蛋白激酶(ERK、MAPK)、磷脂酰肌醇3(PI3)-激酶和p21Ral通路,以及由小GTP酶p21Rho、p21Rac和p21Cdc42调节的其他信号通路。

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