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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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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