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CD95 promotes metastatic spread via Sck in pancreatic ductal adenocarcinoma

Cancer stem cells (CSCs) have been implicated in the initiation and maintenance of tumour growth as well as metastasis. Recent reports link stemness to epithelial–mesenchymal transition (EMT) in cancer. However, there is still little knowledge about the molecular markers of those events. In silico a...

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Autores principales: Teodorczyk, M, Kleber, S, Wollny, D, Sefrin, J P, Aykut, B, Mateos, A, Herhaus, P, Sancho-Martinez, I, Hill, O, Gieffers, C, Sykora, J, Weichert, W, Eisen, C, Trumpp, A, Sprick, M R, Bergmann, F, Welsch, T, Martin-Villalba, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572867/
https://www.ncbi.nlm.nih.gov/pubmed/25613377
http://dx.doi.org/10.1038/cdd.2014.217
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author Teodorczyk, M
Kleber, S
Wollny, D
Sefrin, J P
Aykut, B
Mateos, A
Herhaus, P
Sancho-Martinez, I
Hill, O
Gieffers, C
Sykora, J
Weichert, W
Eisen, C
Trumpp, A
Sprick, M R
Bergmann, F
Welsch, T
Martin-Villalba, A
author_facet Teodorczyk, M
Kleber, S
Wollny, D
Sefrin, J P
Aykut, B
Mateos, A
Herhaus, P
Sancho-Martinez, I
Hill, O
Gieffers, C
Sykora, J
Weichert, W
Eisen, C
Trumpp, A
Sprick, M R
Bergmann, F
Welsch, T
Martin-Villalba, A
author_sort Teodorczyk, M
collection PubMed
description Cancer stem cells (CSCs) have been implicated in the initiation and maintenance of tumour growth as well as metastasis. Recent reports link stemness to epithelial–mesenchymal transition (EMT) in cancer. However, there is still little knowledge about the molecular markers of those events. In silico analysis of RNA profiles of 36 pancreatic ductal adenocarcinomas (PDAC) reveals an association of the expression of CD95 with EMT and stemness that was validated in CSCs isolated from PDAC surgical specimens. CD95 expression was also higher in metastatic pancreatic cells than in primary PDAC. Pharmacological inhibition of CD95 activity reduced PDAC growth and metastasis in CSC-derived xenografts and in a murine syngeneic model. On the mechanistic level, Sck was identified as a novel molecule indispensable for CD95's induction of cell cycle progression. This study uncovers CD95 as a marker of EMT and stemness in PDAC. It also addresses the molecular mechanism by which CD95 drives tumour growth and opens tantalizing therapeutic possibilities in PDAC.
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spelling pubmed-45728672015-09-29 CD95 promotes metastatic spread via Sck in pancreatic ductal adenocarcinoma Teodorczyk, M Kleber, S Wollny, D Sefrin, J P Aykut, B Mateos, A Herhaus, P Sancho-Martinez, I Hill, O Gieffers, C Sykora, J Weichert, W Eisen, C Trumpp, A Sprick, M R Bergmann, F Welsch, T Martin-Villalba, A Cell Death Differ Original Paper Cancer stem cells (CSCs) have been implicated in the initiation and maintenance of tumour growth as well as metastasis. Recent reports link stemness to epithelial–mesenchymal transition (EMT) in cancer. However, there is still little knowledge about the molecular markers of those events. In silico analysis of RNA profiles of 36 pancreatic ductal adenocarcinomas (PDAC) reveals an association of the expression of CD95 with EMT and stemness that was validated in CSCs isolated from PDAC surgical specimens. CD95 expression was also higher in metastatic pancreatic cells than in primary PDAC. Pharmacological inhibition of CD95 activity reduced PDAC growth and metastasis in CSC-derived xenografts and in a murine syngeneic model. On the mechanistic level, Sck was identified as a novel molecule indispensable for CD95's induction of cell cycle progression. This study uncovers CD95 as a marker of EMT and stemness in PDAC. It also addresses the molecular mechanism by which CD95 drives tumour growth and opens tantalizing therapeutic possibilities in PDAC. Nature Publishing Group 2015-07 2015-01-23 /pmc/articles/PMC4572867/ /pubmed/25613377 http://dx.doi.org/10.1038/cdd.2014.217 Text en Copyright © 2015 Macmillan Publishers Limited http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Original Paper
Teodorczyk, M
Kleber, S
Wollny, D
Sefrin, J P
Aykut, B
Mateos, A
Herhaus, P
Sancho-Martinez, I
Hill, O
Gieffers, C
Sykora, J
Weichert, W
Eisen, C
Trumpp, A
Sprick, M R
Bergmann, F
Welsch, T
Martin-Villalba, A
CD95 promotes metastatic spread via Sck in pancreatic ductal adenocarcinoma
title CD95 promotes metastatic spread via Sck in pancreatic ductal adenocarcinoma
title_full CD95 promotes metastatic spread via Sck in pancreatic ductal adenocarcinoma
title_fullStr CD95 promotes metastatic spread via Sck in pancreatic ductal adenocarcinoma
title_full_unstemmed CD95 promotes metastatic spread via Sck in pancreatic ductal adenocarcinoma
title_short CD95 promotes metastatic spread via Sck in pancreatic ductal adenocarcinoma
title_sort cd95 promotes metastatic spread via sck in pancreatic ductal adenocarcinoma
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572867/
https://www.ncbi.nlm.nih.gov/pubmed/25613377
http://dx.doi.org/10.1038/cdd.2014.217
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