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IP-10/CXCL10 attracts regulatory T cells: Implication for pancreatic cancer
Pancreatic stellate cells (PSCs) are key components of pancreatic ductal adenocarcinoma (PDAC). We recently demonstrated that IP-10/CXCL10 is highly expressed by PSCs in the presence of pancreatic cancer cells (PCCs) and its expression correlates with infiltration by regulatory T cells (Tregs) and p...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570127/ https://www.ncbi.nlm.nih.gov/pubmed/26405599 http://dx.doi.org/10.1080/2162402X.2015.1027473 |
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author | Lunardi, Serena Lim, Su Yin Muschel, Ruth J Brunner, Thomas B |
author_facet | Lunardi, Serena Lim, Su Yin Muschel, Ruth J Brunner, Thomas B |
author_sort | Lunardi, Serena |
collection | PubMed |
description | Pancreatic stellate cells (PSCs) are key components of pancreatic ductal adenocarcinoma (PDAC). We recently demonstrated that IP-10/CXCL10 is highly expressed by PSCs in the presence of pancreatic cancer cells (PCCs) and its expression correlates with infiltration by regulatory T cells (Tregs) and poor survival. Thus, stromal cells in pancreatic cancer can promote immunosuppression and tumor progression, through the expression of IP-10. |
format | Online Article Text |
id | pubmed-4570127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-45701272016-02-03 IP-10/CXCL10 attracts regulatory T cells: Implication for pancreatic cancer Lunardi, Serena Lim, Su Yin Muschel, Ruth J Brunner, Thomas B Oncoimmunology Author's View Pancreatic stellate cells (PSCs) are key components of pancreatic ductal adenocarcinoma (PDAC). We recently demonstrated that IP-10/CXCL10 is highly expressed by PSCs in the presence of pancreatic cancer cells (PCCs) and its expression correlates with infiltration by regulatory T cells (Tregs) and poor survival. Thus, stromal cells in pancreatic cancer can promote immunosuppression and tumor progression, through the expression of IP-10. Taylor & Francis 2015-04-02 /pmc/articles/PMC4570127/ /pubmed/26405599 http://dx.doi.org/10.1080/2162402X.2015.1027473 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Author's View Lunardi, Serena Lim, Su Yin Muschel, Ruth J Brunner, Thomas B IP-10/CXCL10 attracts regulatory T cells: Implication for pancreatic cancer |
title | IP-10/CXCL10 attracts regulatory T cells: Implication for pancreatic cancer |
title_full | IP-10/CXCL10 attracts regulatory T cells: Implication for pancreatic cancer |
title_fullStr | IP-10/CXCL10 attracts regulatory T cells: Implication for pancreatic cancer |
title_full_unstemmed | IP-10/CXCL10 attracts regulatory T cells: Implication for pancreatic cancer |
title_short | IP-10/CXCL10 attracts regulatory T cells: Implication for pancreatic cancer |
title_sort | ip-10/cxcl10 attracts regulatory t cells: implication for pancreatic cancer |
topic | Author's View |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570127/ https://www.ncbi.nlm.nih.gov/pubmed/26405599 http://dx.doi.org/10.1080/2162402X.2015.1027473 |
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