Trailblazing LIM kinases take the lead in collective tumor cell invasion

Crighton, D. and Olson, M. F. (2011) Trailblazing LIM kinases take the lead in collective tumor cell invasion. BioArchitecture, 1(1), pp. 5-8. (doi: 10.4161/bioa.1.1.14628) (PMID:21866254) (PMCID:PMC3158634)

[img]
Preview
Text
138823.pdf - Published Version
Available under License Creative Commons Attribution Non-commercial.

1MB

Abstract

The spread of tumor cells from primary sites often occurs as associated cell collectives. In this form of invasion, the contribution of cells leading the way may differ from those that follow. By implication, proteins that regulate the actin cytoskeleton, a major driver of cell motility, may have different roles depending on whether they are in leading or following cells. The LIM kinases 1 and 2 (LIMK) phosphorylate and inactivate the filamentous actin severing function of cofilin proteins. Using siRNA or pharmacological inhibitors, LIMK was found to be required in leading cells of collectively invading tumor cells, or in cancer-associated stromal fibroblasts, for effective extracellular matrix degradation that facilitates three-dimensional invasion. The decreased extracellular matrix degrading activities were associated with an inability to form the stable filamentous actin structures necessary to make matrix-degrading protrusive structures. However, LIMK was not required for cell motility or for path-following in associated collectives. These findings show that leading and following cells in collective invasion have different properties and indicate that targeting the activities in leading cells is sufficient to significantly inhibit tumor cell invasiveness.

Item Type:Articles
Additional Information:This work is supported by Cancer Research UK.
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Crighton, Dr Diane and Olson, Professor Michael
Authors: Crighton, D., and Olson, M. F.
College/School:College of Medical Veterinary and Life Sciences > School of Cancer Sciences
Journal Name:BioArchitecture
Publisher:Taylor & Francis
ISSN:1949-0992
ISSN (Online):1949-100X
Published Online:01 January 2011
Copyright Holders:Copyright © 2011 Landes Bioscience
First Published:First published in BioArchitecture 1(1): 5-8
Publisher Policy:Reproduced under a Creative Commons License

University Staff: Request a correction | Enlighten Editors: Update this record