Tumor promoting effects of CD95 signaling in chemoresistant cells

<p>Abstract</p> <p>Background</p> <p>CD95 is a death receptor controlling not only apoptotic pathways but also activating mechanisms promoting tumor growth. During the acquisition of chemoresistance to oxaliplatin there is a progressive loss of CD95 expression in colon...

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Main Authors: Almendro Vanessa, Gascón Pedro, Pastor-Arroyo Eva, Carbó Neus, Fernández-Nogueira Patricia, Costamagna Domizziana, Mayordomo Cristina, García-Recio Susana, Ametller Elisabet
Format: Article
Language:English
Published: BMC 2010-06-01
Series:Molecular Cancer
Online Access:http://www.molecular-cancer.com/content/9/1/161
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spelling doaj-c5efeded7caa4cb3904225c94c21321b2020-11-25T01:32:29ZengBMCMolecular Cancer1476-45982010-06-019116110.1186/1476-4598-9-161Tumor promoting effects of CD95 signaling in chemoresistant cellsAlmendro VanessaGascón PedroPastor-Arroyo EvaCarbó NeusFernández-Nogueira PatriciaCostamagna DomizzianaMayordomo CristinaGarcía-Recio SusanaAmetller Elisabet<p>Abstract</p> <p>Background</p> <p>CD95 is a death receptor controlling not only apoptotic pathways but also activating mechanisms promoting tumor growth. During the acquisition of chemoresistance to oxaliplatin there is a progressive loss of CD95 expression in colon cancer cells and a decreased ability of this receptor to induce cell death. The aim of this study was to characterize some key cellular responses controlled by CD95 signaling in oxaliplatin-resistant colon cancer cells.</p> <p>Results</p> <p>We show that CD95 triggering results in an increased metastatic ability in resistant cells. Moreover, oxaliplatin treatment itself stimulates cell migration and decreases cell adhesion through CD95 activation, since CD95 expression inhibition by siRNA blocks the promigratory effects of oxaliplatin. These promigratory effects are related to the epithelia-to-mesenchymal transition (EMT) phenomenon, as evidenced by the up-regulation of some transcription factors and mesenchymal markers both <it>in vitro </it>and <it>in vivo</it>.</p> <p>Conclusions</p> <p>We conclude that oxaliplatin treatment in cells that have acquired resistance to oxaliplatin-induced apoptosis results in tumor-promoting effects through the activation of CD95 signaling and by inducing EMT, all these events jointly contributing to a metastatic phenotype.</p> http://www.molecular-cancer.com/content/9/1/161
collection DOAJ
language English
format Article
sources DOAJ
author Almendro Vanessa
Gascón Pedro
Pastor-Arroyo Eva
Carbó Neus
Fernández-Nogueira Patricia
Costamagna Domizziana
Mayordomo Cristina
García-Recio Susana
Ametller Elisabet
spellingShingle Almendro Vanessa
Gascón Pedro
Pastor-Arroyo Eva
Carbó Neus
Fernández-Nogueira Patricia
Costamagna Domizziana
Mayordomo Cristina
García-Recio Susana
Ametller Elisabet
Tumor promoting effects of CD95 signaling in chemoresistant cells
Molecular Cancer
author_facet Almendro Vanessa
Gascón Pedro
Pastor-Arroyo Eva
Carbó Neus
Fernández-Nogueira Patricia
Costamagna Domizziana
Mayordomo Cristina
García-Recio Susana
Ametller Elisabet
author_sort Almendro Vanessa
title Tumor promoting effects of CD95 signaling in chemoresistant cells
title_short Tumor promoting effects of CD95 signaling in chemoresistant cells
title_full Tumor promoting effects of CD95 signaling in chemoresistant cells
title_fullStr Tumor promoting effects of CD95 signaling in chemoresistant cells
title_full_unstemmed Tumor promoting effects of CD95 signaling in chemoresistant cells
title_sort tumor promoting effects of cd95 signaling in chemoresistant cells
publisher BMC
series Molecular Cancer
issn 1476-4598
publishDate 2010-06-01
description <p>Abstract</p> <p>Background</p> <p>CD95 is a death receptor controlling not only apoptotic pathways but also activating mechanisms promoting tumor growth. During the acquisition of chemoresistance to oxaliplatin there is a progressive loss of CD95 expression in colon cancer cells and a decreased ability of this receptor to induce cell death. The aim of this study was to characterize some key cellular responses controlled by CD95 signaling in oxaliplatin-resistant colon cancer cells.</p> <p>Results</p> <p>We show that CD95 triggering results in an increased metastatic ability in resistant cells. Moreover, oxaliplatin treatment itself stimulates cell migration and decreases cell adhesion through CD95 activation, since CD95 expression inhibition by siRNA blocks the promigratory effects of oxaliplatin. These promigratory effects are related to the epithelia-to-mesenchymal transition (EMT) phenomenon, as evidenced by the up-regulation of some transcription factors and mesenchymal markers both <it>in vitro </it>and <it>in vivo</it>.</p> <p>Conclusions</p> <p>We conclude that oxaliplatin treatment in cells that have acquired resistance to oxaliplatin-induced apoptosis results in tumor-promoting effects through the activation of CD95 signaling and by inducing EMT, all these events jointly contributing to a metastatic phenotype.</p>
url http://www.molecular-cancer.com/content/9/1/161
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