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FAK-inhibition opens the door to checkpoint immunotherapy in Pancreatic Cancer
Immunotherapy has had remarkable success in the treatment of some cancer types. However, pancreatic cancer has remained largely refractory to immunotherapy, including immune checkpoint inhibitors. Recently, Jiang and colleagues identified a key role for FAK in regulating the composition of the fibro...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319091/ https://www.ncbi.nlm.nih.gov/pubmed/28239470 http://dx.doi.org/10.1186/s40425-017-0217-6 |
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author | Symeonides, Stefan N. Anderton, Stephen M. Serrels, Alan |
author_facet | Symeonides, Stefan N. Anderton, Stephen M. Serrels, Alan |
author_sort | Symeonides, Stefan N. |
collection | PubMed |
description | Immunotherapy has had remarkable success in the treatment of some cancer types. However, pancreatic cancer has remained largely refractory to immunotherapy, including immune checkpoint inhibitors. Recently, Jiang and colleagues identified a key role for FAK in regulating the composition of the fibrotic and immuno-suppressive pancreatic tumour niche, and showed that FAK inhibitors can be used in combination with immune checkpoint blockade and gemcitabine chemotherapy to significantly delay pancreatic tumour progression. This study further supports the use of FAK inhibitors in combination with immunotherapy. |
format | Online Article Text |
id | pubmed-5319091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53190912017-02-24 FAK-inhibition opens the door to checkpoint immunotherapy in Pancreatic Cancer Symeonides, Stefan N. Anderton, Stephen M. Serrels, Alan J Immunother Cancer Commentary Immunotherapy has had remarkable success in the treatment of some cancer types. However, pancreatic cancer has remained largely refractory to immunotherapy, including immune checkpoint inhibitors. Recently, Jiang and colleagues identified a key role for FAK in regulating the composition of the fibrotic and immuno-suppressive pancreatic tumour niche, and showed that FAK inhibitors can be used in combination with immune checkpoint blockade and gemcitabine chemotherapy to significantly delay pancreatic tumour progression. This study further supports the use of FAK inhibitors in combination with immunotherapy. BioMed Central 2017-02-21 /pmc/articles/PMC5319091/ /pubmed/28239470 http://dx.doi.org/10.1186/s40425-017-0217-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Commentary Symeonides, Stefan N. Anderton, Stephen M. Serrels, Alan FAK-inhibition opens the door to checkpoint immunotherapy in Pancreatic Cancer |
title | FAK-inhibition opens the door to checkpoint immunotherapy in Pancreatic Cancer |
title_full | FAK-inhibition opens the door to checkpoint immunotherapy in Pancreatic Cancer |
title_fullStr | FAK-inhibition opens the door to checkpoint immunotherapy in Pancreatic Cancer |
title_full_unstemmed | FAK-inhibition opens the door to checkpoint immunotherapy in Pancreatic Cancer |
title_short | FAK-inhibition opens the door to checkpoint immunotherapy in Pancreatic Cancer |
title_sort | fak-inhibition opens the door to checkpoint immunotherapy in pancreatic cancer |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319091/ https://www.ncbi.nlm.nih.gov/pubmed/28239470 http://dx.doi.org/10.1186/s40425-017-0217-6 |
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