Signalling to cancer cell invasion through PAK family kinases

被引:77
作者
Whale, Andrew [2 ]
Hashim, Fariesha Nur [1 ]
Fram, Sally [1 ]
Jones, Gareth E. [2 ]
Wells, Claire M. [1 ]
机构
[1] Kings Coll London, Div Canc Studies, London SE1 1UL, England
[2] Kings Coll London, Randall Div Cell & Mol Biophys, London SE1 1UL, England
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2011年 / 16卷
关键词
PAK; Cancer; Invasion; Migration; Actin; Review; P21-ACTIVATED PROTEIN-KINASE; ANCHORAGE-INDEPENDENT GROWTH; LIGHT-CHAIN KINASE; P85; BETA-PIX; PROSTATE-CANCER; LIM-KINASE; SERINE/THREONINE KINASE; ACTIN CYTOSKELETON; COLORECTAL-CANCER; TYROSINE KINASE;
D O I
10.2741/3724
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:849 / 864
页数:16
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