Cargando…

Tumour immune escape via P2X7 receptor signalling

While P2X7 receptor expression on tumour cells has been characterized as a promotor of cancer growth and metastasis, its expression by the host immune system is central for orchestration of both innate and adaptive immune responses against cancer. The role of P2X7R in anti-tumour immunity is complex...

Descripción completa

Detalles Bibliográficos
Autores principales: Sainz, Ricardo M., Rodriguez-Quintero, Jorge Humberto, Maldifassi, Maria Constanza, Stiles, Brendon M., Wennerberg, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643160/
https://www.ncbi.nlm.nih.gov/pubmed/38022596
http://dx.doi.org/10.3389/fimmu.2023.1287310
_version_ 1785134294332604416
author Sainz, Ricardo M.
Rodriguez-Quintero, Jorge Humberto
Maldifassi, Maria Constanza
Stiles, Brendon M.
Wennerberg, Erik
author_facet Sainz, Ricardo M.
Rodriguez-Quintero, Jorge Humberto
Maldifassi, Maria Constanza
Stiles, Brendon M.
Wennerberg, Erik
author_sort Sainz, Ricardo M.
collection PubMed
description While P2X7 receptor expression on tumour cells has been characterized as a promotor of cancer growth and metastasis, its expression by the host immune system is central for orchestration of both innate and adaptive immune responses against cancer. The role of P2X7R in anti-tumour immunity is complex and preclinical studies have described opposing roles of the P2X7R in regulating immune responses against tumours. Therefore, few P2X7R modulators have reached clinical testing in cancer patients. Here, we review the prognostic value of P2X7R in cancer, how P2X7R have been targeted to date in tumour models, and we discuss four aspects of how tumours skew immune responses to promote immune escape via the P2X7R; non-pore functional P2X7Rs, mono-ADP-ribosyltransferases, ectonucleotidases, and immunoregulatory cells. Lastly, we discuss alternative approaches to offset tumour immune escape via P2X7R to enhance immunotherapeutic strategies in cancer patients.
format Online
Article
Text
id pubmed-10643160
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-106431602023-01-01 Tumour immune escape via P2X7 receptor signalling Sainz, Ricardo M. Rodriguez-Quintero, Jorge Humberto Maldifassi, Maria Constanza Stiles, Brendon M. Wennerberg, Erik Front Immunol Immunology While P2X7 receptor expression on tumour cells has been characterized as a promotor of cancer growth and metastasis, its expression by the host immune system is central for orchestration of both innate and adaptive immune responses against cancer. The role of P2X7R in anti-tumour immunity is complex and preclinical studies have described opposing roles of the P2X7R in regulating immune responses against tumours. Therefore, few P2X7R modulators have reached clinical testing in cancer patients. Here, we review the prognostic value of P2X7R in cancer, how P2X7R have been targeted to date in tumour models, and we discuss four aspects of how tumours skew immune responses to promote immune escape via the P2X7R; non-pore functional P2X7Rs, mono-ADP-ribosyltransferases, ectonucleotidases, and immunoregulatory cells. Lastly, we discuss alternative approaches to offset tumour immune escape via P2X7R to enhance immunotherapeutic strategies in cancer patients. Frontiers Media S.A. 2023-10-30 /pmc/articles/PMC10643160/ /pubmed/38022596 http://dx.doi.org/10.3389/fimmu.2023.1287310 Text en Copyright © 2023 Sainz, Rodriguez-Quintero, Maldifassi, Stiles and Wennerberg https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Sainz, Ricardo M.
Rodriguez-Quintero, Jorge Humberto
Maldifassi, Maria Constanza
Stiles, Brendon M.
Wennerberg, Erik
Tumour immune escape via P2X7 receptor signalling
title Tumour immune escape via P2X7 receptor signalling
title_full Tumour immune escape via P2X7 receptor signalling
title_fullStr Tumour immune escape via P2X7 receptor signalling
title_full_unstemmed Tumour immune escape via P2X7 receptor signalling
title_short Tumour immune escape via P2X7 receptor signalling
title_sort tumour immune escape via p2x7 receptor signalling
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643160/
https://www.ncbi.nlm.nih.gov/pubmed/38022596
http://dx.doi.org/10.3389/fimmu.2023.1287310
work_keys_str_mv AT sainzricardom tumourimmuneescapeviap2x7receptorsignalling
AT rodriguezquinterojorgehumberto tumourimmuneescapeviap2x7receptorsignalling
AT maldifassimariaconstanza tumourimmuneescapeviap2x7receptorsignalling
AT stilesbrendonm tumourimmuneescapeviap2x7receptorsignalling
AT wennerbergerik tumourimmuneescapeviap2x7receptorsignalling