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The ART of tumor immune escape
We recently identified the adenosine-5′-diphosphate (ADP)–ribosyltransferase-1 (ART1) as a novel immune checkpoint expressed by cancer cells. ART1 utilizes free nicotinamide adenine dinucleotide (NAD(+)) in the tumor microenvironment (TME) to mono-ADP-ribosylate (MARylate) the P2X7 receptor (P2X7R)...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116389/ https://www.ncbi.nlm.nih.gov/pubmed/35602287 http://dx.doi.org/10.1080/2162402X.2022.2076310 |
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author | Wennerberg, Erik Mukherjee, Sumit Sainz, Ricardo M. Stiles, Brendon M. |
author_facet | Wennerberg, Erik Mukherjee, Sumit Sainz, Ricardo M. Stiles, Brendon M. |
author_sort | Wennerberg, Erik |
collection | PubMed |
description | We recently identified the adenosine-5′-diphosphate (ADP)–ribosyltransferase-1 (ART1) as a novel immune checkpoint expressed by cancer cells. ART1 utilizes free nicotinamide adenine dinucleotide (NAD(+)) in the tumor microenvironment (TME) to mono-ADP-ribosylate (MARylate) the P2X7 receptor (P2X7R) on CD8 T cells, resulting in NAD-induced cell death (NICD) and tumor immune resistance. This process is blocked by therapeutic antibody targeting of ART1. |
format | Online Article Text |
id | pubmed-9116389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-91163892022-05-19 The ART of tumor immune escape Wennerberg, Erik Mukherjee, Sumit Sainz, Ricardo M. Stiles, Brendon M. Oncoimmunology Author’s View We recently identified the adenosine-5′-diphosphate (ADP)–ribosyltransferase-1 (ART1) as a novel immune checkpoint expressed by cancer cells. ART1 utilizes free nicotinamide adenine dinucleotide (NAD(+)) in the tumor microenvironment (TME) to mono-ADP-ribosylate (MARylate) the P2X7 receptor (P2X7R) on CD8 T cells, resulting in NAD-induced cell death (NICD) and tumor immune resistance. This process is blocked by therapeutic antibody targeting of ART1. Taylor & Francis 2022-05-14 /pmc/articles/PMC9116389/ /pubmed/35602287 http://dx.doi.org/10.1080/2162402X.2022.2076310 Text en © 2022 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Author’s View Wennerberg, Erik Mukherjee, Sumit Sainz, Ricardo M. Stiles, Brendon M. The ART of tumor immune escape |
title | The ART of tumor immune escape |
title_full | The ART of tumor immune escape |
title_fullStr | The ART of tumor immune escape |
title_full_unstemmed | The ART of tumor immune escape |
title_short | The ART of tumor immune escape |
title_sort | art of tumor immune escape |
topic | Author’s View |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116389/ https://www.ncbi.nlm.nih.gov/pubmed/35602287 http://dx.doi.org/10.1080/2162402X.2022.2076310 |
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