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PMID: 14999155 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Molecular basis for Rho GTPase signaling specificity.

Breast cancer research and treatment ·Vol. 84 ·No. 1 ·2004-03-00 ·Pages 61-71

Karnoub AE, Symons M, Campbell SL, Der CJ

Abstract

There is now considerable evidence for the involvement of aberrant Rho GTPase activation in breast cancer development. Like Ras, Rho GTPases function as signaling nodes regulated by diverse extracellular stimuli. Rho GTPase activation is facilitated by multiple regulatory proteins, in particular guanine nucleotide exchange factors (GEFs) such as Dbl family proteins. Activated Rho GTPases in turn interact with and regulate a spectrum of functionally diverse downstream effectors, initiating a network of cytoplasmic and nuclear signaling cascades. Thus, Rho GTPases represent points of signaling convergence as well as relay switches that disseminate signaling divergence. In this review, we highlight issues relating to the structural basis by which Dbl family GEFs facilitate signaling convergence and Rho GTPase activation, and how Rho GTPases promote signal dissemination through downstream effectors.

MeSH Terms
Breast Neoplasms/enzymology,pathology,physiopathology Enzyme Activation/physiology Female GTPase-Activating Proteins/physiology Guanine Nucleotide Dissociation Inhibitors/physiology Guanine Nucleotide Exchange Factors/physiology Humans Mutation Signal Transduction/physiology rho GTP-Binding Proteins/genetics,physiology
Chemicals
GTPase-Activating Proteins Guanine Nucleotide Dissociation Inhibitors Guanine Nucleotide Exchange Factors rho GTP-Binding Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Karnoub Antoine E
Department of Pharmacology, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7295, USA.
Symons Marc
Campbell Sharon L
Der Channing J
Article Info
Journal
Breast cancer research and treatment
Abbr.
Breast Cancer Res Treat
ISSN
0167-6806
Published
2004-03-00
Pages
61-71
Language
English
Region
Netherlands
NLM ID
8111104
Subset
IM
Grants
NCI NIH HHS · CA63071 · United States
NCI NIH HHS · CA92240 · United States
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