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A sticky situation: CCN1 promotes both proliferation and apoptosis of cancer cells

Members of the CCN family of matricellular signaling regulators promote cell adhesion through integrins and heparan sulfate-containing proteoglycans. A paradox of the CCN field is that, depending on the set of circumstances examined, individual CCN molecules can have quite different, and often oppos...

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Detalles Bibliográficos
Autor principal: Leask, Andrew
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821478/
https://www.ncbi.nlm.nih.gov/pubmed/19834822
http://dx.doi.org/10.1007/s12079-009-0079-x
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author Leask, Andrew
author_facet Leask, Andrew
author_sort Leask, Andrew
collection PubMed
description Members of the CCN family of matricellular signaling regulators promote cell adhesion through integrins and heparan sulfate-containing proteoglycans. A paradox of the CCN field is that, depending on the set of circumstances examined, individual CCN molecules can have quite different, and often opposing, effects. In a recent report, Franzen and colleagues (Mol Cancer Res. 7:1045–1055, 2009) show using siRNA knockdown that CCN1 (cyr61) is essential for the proliferation of prostate cancer cells. Intriguingly, on the other hand, CCN1 also enhances TRAIL-induced apoptosis. Thus the utility of anti-CCN1 therapy in cancer needs to be carefully considered in light of these divergent results. The significance of this paper is discussed.
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spelling pubmed-28214782010-02-19 A sticky situation: CCN1 promotes both proliferation and apoptosis of cancer cells Leask, Andrew J Cell Commun Signal Bits and Bytes Members of the CCN family of matricellular signaling regulators promote cell adhesion through integrins and heparan sulfate-containing proteoglycans. A paradox of the CCN field is that, depending on the set of circumstances examined, individual CCN molecules can have quite different, and often opposing, effects. In a recent report, Franzen and colleagues (Mol Cancer Res. 7:1045–1055, 2009) show using siRNA knockdown that CCN1 (cyr61) is essential for the proliferation of prostate cancer cells. Intriguingly, on the other hand, CCN1 also enhances TRAIL-induced apoptosis. Thus the utility of anti-CCN1 therapy in cancer needs to be carefully considered in light of these divergent results. The significance of this paper is discussed. Springer Netherlands 2009-10-16 2010-03 /pmc/articles/PMC2821478/ /pubmed/19834822 http://dx.doi.org/10.1007/s12079-009-0079-x Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Bits and Bytes
Leask, Andrew
A sticky situation: CCN1 promotes both proliferation and apoptosis of cancer cells
title A sticky situation: CCN1 promotes both proliferation and apoptosis of cancer cells
title_full A sticky situation: CCN1 promotes both proliferation and apoptosis of cancer cells
title_fullStr A sticky situation: CCN1 promotes both proliferation and apoptosis of cancer cells
title_full_unstemmed A sticky situation: CCN1 promotes both proliferation and apoptosis of cancer cells
title_short A sticky situation: CCN1 promotes both proliferation and apoptosis of cancer cells
title_sort sticky situation: ccn1 promotes both proliferation and apoptosis of cancer cells
topic Bits and Bytes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821478/
https://www.ncbi.nlm.nih.gov/pubmed/19834822
http://dx.doi.org/10.1007/s12079-009-0079-x
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