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PMID: 15736063 Published · ppublish English Journal Article Review

The signaling network of tumor invasion.

Histology and histopathology ·Vol. 20 ·No. 2 ·2005-00-00 ·Pages 593-602

Wang GK, Zhang W

Abstract

The ability of a cell to invade its surroundings is an important hallmark of malignant tumors and results from aberrant cell signaling mechanisms. The signal transduction that leads to tumor invasion can be broken down into major pathways. Even though the pathway systems are distinct in themselves, none of these pathways operate independently when it comes to transmitting signals that culminate in an invasive phenotype. That is, the malignant change in one receptor not only leads to malignant changes directly downstream but can also affect the molecules of many other pathways. Three major pathway systems involved in tumor invasion are discussed in this review: the integrin system, the insulin-like growth factor system, and the Rho family GTPases. Here we see that although the individual signaling systems can each contribute to invasion, each system is networked to others and should not be considered isolated. Each system is first reviewed as independent contributors to an invasive phenotype and then discussed in the context of interacting pathways that collectively result in tumor invasion.

MeSH Terms
Animals Feedback Humans Integrins/physiology Models, Biological Neoplasm Invasiveness/physiopathology Receptor Cross-Talk/physiology Signal Transduction/physiology Somatomedins/physiology rho GTP-Binding Proteins/physiology
Chemicals
Integrins Somatomedins rho GTP-Binding Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Wang G K
Department of Pathology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, USA.
Zhang W
Article Info
Journal
Histology and histopathology
Abbr.
Histol Histopathol
ISSN
0213-3911
Published
2005-00-00
Pages
593-602
Language
English
Region
Spain
NLM ID
8609357
Subset
IM
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