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Syndecans in tumor cell adhesion and signaling

Anchorage of cells to "heparin" – binding domains that are prevalent in extracellular matrix (ECM) components is thought to occur primarily through the syndecans, a four-member family of transmembrane heparan sulfate proteoglycans that communicate environmental cues from the ECM to the cyt...

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Autores principales: Beauvais, DeannaLee M, Rapraeger, Alan C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC320497/
https://www.ncbi.nlm.nih.gov/pubmed/14711376
http://dx.doi.org/10.1186/1477-7827-2-3
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author Beauvais, DeannaLee M
Rapraeger, Alan C
author_facet Beauvais, DeannaLee M
Rapraeger, Alan C
author_sort Beauvais, DeannaLee M
collection PubMed
description Anchorage of cells to "heparin" – binding domains that are prevalent in extracellular matrix (ECM) components is thought to occur primarily through the syndecans, a four-member family of transmembrane heparan sulfate proteoglycans that communicate environmental cues from the ECM to the cytoskeleton and the signaling apparatus of the cell. Known activities of the syndecans trace to their highly conserved cytoplasmic domains and to their heparan sulfate chains, which can serve to regulate the signaling of growth factors and morphogens. However, several emerging studies point to critical roles for the syndecans' extracellular protein domains in tumor cell behavior to include cell adhesion and invasion. Although the mechanisms of these activities remain largely unknown, one possibility involves "co-receptor" interactions with integrins that may regulate integrin function and the cell adhesion-signaling phenotype. Thus, alterations in syndecan expression, leading to either overexpression or loss of expression, both of which take place in tumor cells, may have dramatic effects on tumor cell invasion.
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spelling pubmed-3204972004-01-28 Syndecans in tumor cell adhesion and signaling Beauvais, DeannaLee M Rapraeger, Alan C Reprod Biol Endocrinol Review Anchorage of cells to "heparin" – binding domains that are prevalent in extracellular matrix (ECM) components is thought to occur primarily through the syndecans, a four-member family of transmembrane heparan sulfate proteoglycans that communicate environmental cues from the ECM to the cytoskeleton and the signaling apparatus of the cell. Known activities of the syndecans trace to their highly conserved cytoplasmic domains and to their heparan sulfate chains, which can serve to regulate the signaling of growth factors and morphogens. However, several emerging studies point to critical roles for the syndecans' extracellular protein domains in tumor cell behavior to include cell adhesion and invasion. Although the mechanisms of these activities remain largely unknown, one possibility involves "co-receptor" interactions with integrins that may regulate integrin function and the cell adhesion-signaling phenotype. Thus, alterations in syndecan expression, leading to either overexpression or loss of expression, both of which take place in tumor cells, may have dramatic effects on tumor cell invasion. BioMed Central 2004-01-07 /pmc/articles/PMC320497/ /pubmed/14711376 http://dx.doi.org/10.1186/1477-7827-2-3 Text en Copyright © 2004 Beauvais and Rapraeger; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Review
Beauvais, DeannaLee M
Rapraeger, Alan C
Syndecans in tumor cell adhesion and signaling
title Syndecans in tumor cell adhesion and signaling
title_full Syndecans in tumor cell adhesion and signaling
title_fullStr Syndecans in tumor cell adhesion and signaling
title_full_unstemmed Syndecans in tumor cell adhesion and signaling
title_short Syndecans in tumor cell adhesion and signaling
title_sort syndecans in tumor cell adhesion and signaling
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC320497/
https://www.ncbi.nlm.nih.gov/pubmed/14711376
http://dx.doi.org/10.1186/1477-7827-2-3
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