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YAP Attenuates CD8 T Cell-Mediated Anti-tumor Response

YAP is a transcriptional coactivator of the Hippo signaling pathway that has largely been studied for its role in the regulation of organ size during development. Several studies have shown that YAP is upregulated in cancer cells, and more recently in the T regulatory (Treg) subset of CD4+ cells. Th...

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Autores principales: Lebid, Andriana, Chung, Liam, Pardoll, Drew M., Pan, Fan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158852/
https://www.ncbi.nlm.nih.gov/pubmed/32322254
http://dx.doi.org/10.3389/fimmu.2020.00580
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author Lebid, Andriana
Chung, Liam
Pardoll, Drew M.
Pan, Fan
author_facet Lebid, Andriana
Chung, Liam
Pardoll, Drew M.
Pan, Fan
author_sort Lebid, Andriana
collection PubMed
description YAP is a transcriptional coactivator of the Hippo signaling pathway that has largely been studied for its role in the regulation of organ size during development. Several studies have shown that YAP is upregulated in cancer cells, and more recently in the T regulatory (Treg) subset of CD4+ cells. These observations suggest that the transcriptional co-activator may promote tumor persistence and progression. Here, we report that YAP also plays an immunoinhibitory role in CD8 T cells, especially in activated cytotoxic cells usually found in the tumor microenvironment. Our findings add further rationale for the development and use of pharmacologic inhibitors of YAP to treat cancer.
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spelling pubmed-71588522020-04-22 YAP Attenuates CD8 T Cell-Mediated Anti-tumor Response Lebid, Andriana Chung, Liam Pardoll, Drew M. Pan, Fan Front Immunol Immunology YAP is a transcriptional coactivator of the Hippo signaling pathway that has largely been studied for its role in the regulation of organ size during development. Several studies have shown that YAP is upregulated in cancer cells, and more recently in the T regulatory (Treg) subset of CD4+ cells. These observations suggest that the transcriptional co-activator may promote tumor persistence and progression. Here, we report that YAP also plays an immunoinhibitory role in CD8 T cells, especially in activated cytotoxic cells usually found in the tumor microenvironment. Our findings add further rationale for the development and use of pharmacologic inhibitors of YAP to treat cancer. Frontiers Media S.A. 2020-04-08 /pmc/articles/PMC7158852/ /pubmed/32322254 http://dx.doi.org/10.3389/fimmu.2020.00580 Text en Copyright © 2020 Lebid, Chung, Pardoll and Pan. http://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
Lebid, Andriana
Chung, Liam
Pardoll, Drew M.
Pan, Fan
YAP Attenuates CD8 T Cell-Mediated Anti-tumor Response
title YAP Attenuates CD8 T Cell-Mediated Anti-tumor Response
title_full YAP Attenuates CD8 T Cell-Mediated Anti-tumor Response
title_fullStr YAP Attenuates CD8 T Cell-Mediated Anti-tumor Response
title_full_unstemmed YAP Attenuates CD8 T Cell-Mediated Anti-tumor Response
title_short YAP Attenuates CD8 T Cell-Mediated Anti-tumor Response
title_sort yap attenuates cd8 t cell-mediated anti-tumor response
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158852/
https://www.ncbi.nlm.nih.gov/pubmed/32322254
http://dx.doi.org/10.3389/fimmu.2020.00580
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