Document Detail


Mechanical signaling through the cytoskeleton regulates cell proliferation by coordinated focal adhesion and Rho GTPase signaling.
MedLine Citation:
PMID:  21444750     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The notion that cell shape and spreading can regulate cell proliferation has evolved over several years, but only recently has this been linked to forces from within and upon the cell. This emerging area of mechanical signaling is proving to be wide-spread and important for all cell types. The microenvironment that surrounds cells provides a complex spectrum of different, simultaneously active, biochemical, structural and mechanical stimuli. In this milieu, cells probe the stiffness of their microenvironment by pulling on the extracellular matrix (ECM) and/or adjacent cells. This process is dependent on transcellular cell-ECM or cell-cell adhesions, as well as cell contractility mediated by Rho GTPases, to provide a functional linkage through which forces are transmitted through the cytoskeleton by intracellular force-generating proteins. This Commentary covers recent advances in the underlying mechanisms that control cell proliferation by mechanical signaling, with an emphasis on the role of 3D microenvironments and in vivo extracellular matrices. Moreover, as there is much recent interest in the tumor-stromal interaction, we will pay particular attention to exciting new data describing the role of mechanical signaling in the progression of breast cancer.
Authors:
Paolo P Provenzano; Patricia J Keely
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural    
Journal Detail:
Title:  Journal of cell science     Volume:  124     ISSN:  1477-9137     ISO Abbreviation:  J. Cell. Sci.     Publication Date:  2011 Apr 
Date Detail:
Created Date:  2011-03-29     Completed Date:  2011-09-02     Revised Date:  2012-04-16    
Medline Journal Info:
Nlm Unique ID:  0052457     Medline TA:  J Cell Sci     Country:  England    
Other Details:
Languages:  eng     Pagination:  1195-205     Citation Subset:  IM    
Affiliation:
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. ppproven@fhcrc.org
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MeSH Terms
Descriptor/Qualifier:
Animals
Cell Proliferation*
Cytoskeleton / enzymology,  genetics,  metabolism*
Focal Adhesions / enzymology*,  metabolism*
Humans
Mechanotransduction, Cellular*
Neoplasms / enzymology,  genetics,  metabolism*
Signal Transduction
rho GTP-Binding Proteins / genetics,  metabolism*
Grant Support
ID/Acronym/Agency:
CA114462/CA/NCI NIH HHS; CA142833/CA/NCI NIH HHS; CA152249/CA/NCI NIH HHS; R21 CA152249-02/CA/NCI NIH HHS
Chemical
Reg. No./Substance:
EC 3.6.5.2/rho GTP-Binding Proteins

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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