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CD73-Generated Adenosine: Orchestrating the Tumor-Stroma Interplay to Promote Cancer Growth

Despite the coming of age of cancer immunotherapy, clinical benefits are still modest. An important barrier to successful cancer immunotherapy is that tumors employ a number of mechanisms to facilitate immune escape, including the production of anti-inflammatory cytokines, the recruitment of regulat...

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Detalles Bibliográficos
Autores principales: Allard, Bertrand, Turcotte, Martin, Stagg, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482007/
https://www.ncbi.nlm.nih.gov/pubmed/23125525
http://dx.doi.org/10.1155/2012/485156
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author Allard, Bertrand
Turcotte, Martin
Stagg, John
author_facet Allard, Bertrand
Turcotte, Martin
Stagg, John
author_sort Allard, Bertrand
collection PubMed
description Despite the coming of age of cancer immunotherapy, clinical benefits are still modest. An important barrier to successful cancer immunotherapy is that tumors employ a number of mechanisms to facilitate immune escape, including the production of anti-inflammatory cytokines, the recruitment of regulatory immune subsets, and the production of immunosuppressive metabolites. Significant therapeutic opportunity exists in targeting these immunosuppressive pathways. One such immunosuppressive pathway is the production of extracellular adenosine by CD73, an ectonucleotidase overexpressed in various types of cancer. We hereafter review the biology of CD73 and its role in cancer progression and metastasis. We describe the role of extracellular adenosine in promoting tumor growth through paracrine and autocrine action on tumor cells, endothelial cells, and immune cells.
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spelling pubmed-34820072012-11-02 CD73-Generated Adenosine: Orchestrating the Tumor-Stroma Interplay to Promote Cancer Growth Allard, Bertrand Turcotte, Martin Stagg, John J Biomed Biotechnol Review Article Despite the coming of age of cancer immunotherapy, clinical benefits are still modest. An important barrier to successful cancer immunotherapy is that tumors employ a number of mechanisms to facilitate immune escape, including the production of anti-inflammatory cytokines, the recruitment of regulatory immune subsets, and the production of immunosuppressive metabolites. Significant therapeutic opportunity exists in targeting these immunosuppressive pathways. One such immunosuppressive pathway is the production of extracellular adenosine by CD73, an ectonucleotidase overexpressed in various types of cancer. We hereafter review the biology of CD73 and its role in cancer progression and metastasis. We describe the role of extracellular adenosine in promoting tumor growth through paracrine and autocrine action on tumor cells, endothelial cells, and immune cells. Hindawi Publishing Corporation 2012 2012-10-16 /pmc/articles/PMC3482007/ /pubmed/23125525 http://dx.doi.org/10.1155/2012/485156 Text en Copyright © 2012 Bertrand Allard et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Allard, Bertrand
Turcotte, Martin
Stagg, John
CD73-Generated Adenosine: Orchestrating the Tumor-Stroma Interplay to Promote Cancer Growth
title CD73-Generated Adenosine: Orchestrating the Tumor-Stroma Interplay to Promote Cancer Growth
title_full CD73-Generated Adenosine: Orchestrating the Tumor-Stroma Interplay to Promote Cancer Growth
title_fullStr CD73-Generated Adenosine: Orchestrating the Tumor-Stroma Interplay to Promote Cancer Growth
title_full_unstemmed CD73-Generated Adenosine: Orchestrating the Tumor-Stroma Interplay to Promote Cancer Growth
title_short CD73-Generated Adenosine: Orchestrating the Tumor-Stroma Interplay to Promote Cancer Growth
title_sort cd73-generated adenosine: orchestrating the tumor-stroma interplay to promote cancer growth
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482007/
https://www.ncbi.nlm.nih.gov/pubmed/23125525
http://dx.doi.org/10.1155/2012/485156
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