Randall Division of Cell and Molecular Biophysics, King's College London, London.
Front Biosci (Landmark Ed). 2011 Jan 1;16(3):849-64. doi: 10.2741/3724.
Cancer cell metastasis involves a series of changes in cell behaviour, driven by oncogenic transformation, that leads to local tissue invasion, migration through extracellular matrix, entry into the vascular or lymphatic system and colonisation of distant sites. It is well established that the Rho family GTPases Rho, Rac and Cdc42 orchestrate many of the processes required during metastasis. The Rho family GTPases regulate cellular behaviour through their interaction with downstream effector proteins. The p-21 activated kinases (PAKs), effector proteins for Rac and Cdc42, are known to be important regulators of cell migration and invasion. There are six mammalian PAKs which can be divided into two groups: group I PAKs (PAK1-3) and group II PAKs (PAK4-6). Although the two PAK groups are architecturally similar there are differences in their mode of regulation suggesting their cellular functions are likely to be different. This review will focus on the latest evidence relating to the role of PAK family kinases in the cell signalling pathways that drive cancer cell migration and invasion.
癌细胞转移涉及一系列细胞行为的变化,这些变化是由致癌转化驱动的,导致局部组织侵袭、穿过细胞外基质迁移、进入血管或淋巴管系统以及在远处部位定植。已经证实,Rho 家族 GTPases Rho、Rac 和 Cdc42 协调转移过程中所需的许多过程。Rho 家族 GTPases 通过与下游效应蛋白相互作用来调节细胞行为。p21 激活激酶(PAKs)是 Rac 和 Cdc42 的效应蛋白,是细胞迁移和侵袭的重要调节因子。有六种哺乳动物 PAKs,可以分为两组:I 组 PAKs(PAK1-3)和 II 组 PAKs(PAK4-6)。尽管两组 PAK 在结构上相似,但它们的调节方式存在差异,表明它们的细胞功能可能不同。这篇综述将重点介绍与 PAK 家族激酶在驱动癌细胞迁移和侵袭的细胞信号通路中的作用相关的最新证据。