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A(2A) blockade enhances anti-metastatic immune responses
The specific targeting of tumor-elicited immunosuppression is a promising strategy for the treatment of cancer. We have recently demonstrated that targeting the immunosuppressive pathway mediated by CD73-derived adenosine through the blockade of A(2A)/A(2B) adenosine receptors significantly reduced...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926871/ https://www.ncbi.nlm.nih.gov/pubmed/24575377 http://dx.doi.org/10.4161/onci.26705 |
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author | Beavis, Paul A Milenkovski, Nicole Stagg, John Smyth, Mark J Darcy, Phillip K |
author_facet | Beavis, Paul A Milenkovski, Nicole Stagg, John Smyth, Mark J Darcy, Phillip K |
author_sort | Beavis, Paul A |
collection | PubMed |
description | The specific targeting of tumor-elicited immunosuppression is a promising strategy for the treatment of cancer. We have recently demonstrated that targeting the immunosuppressive pathway mediated by CD73-derived adenosine through the blockade of A(2A)/A(2B) adenosine receptors significantly reduced the metastatic potential of CD73(+) breast carcinomas and melanomas via both immunological and non-immunological mechanisms. |
format | Online Article Text |
id | pubmed-3926871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-39268712014-02-26 A(2A) blockade enhances anti-metastatic immune responses Beavis, Paul A Milenkovski, Nicole Stagg, John Smyth, Mark J Darcy, Phillip K Oncoimmunology Author's View The specific targeting of tumor-elicited immunosuppression is a promising strategy for the treatment of cancer. We have recently demonstrated that targeting the immunosuppressive pathway mediated by CD73-derived adenosine through the blockade of A(2A)/A(2B) adenosine receptors significantly reduced the metastatic potential of CD73(+) breast carcinomas and melanomas via both immunological and non-immunological mechanisms. Landes Bioscience 2013-12-01 2013-10-22 /pmc/articles/PMC3926871/ /pubmed/24575377 http://dx.doi.org/10.4161/onci.26705 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Author's View Beavis, Paul A Milenkovski, Nicole Stagg, John Smyth, Mark J Darcy, Phillip K A(2A) blockade enhances anti-metastatic immune responses |
title | A(2A) blockade enhances anti-metastatic immune responses |
title_full | A(2A) blockade enhances anti-metastatic immune responses |
title_fullStr | A(2A) blockade enhances anti-metastatic immune responses |
title_full_unstemmed | A(2A) blockade enhances anti-metastatic immune responses |
title_short | A(2A) blockade enhances anti-metastatic immune responses |
title_sort | a(2a) blockade enhances anti-metastatic immune responses |
topic | Author's View |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926871/ https://www.ncbi.nlm.nih.gov/pubmed/24575377 http://dx.doi.org/10.4161/onci.26705 |
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