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Programmed Death-Ligand 1 as a Regulator of Tumor Progression and Metastasis

Programmed cell death protein 1 (PD-1)/programmed death-ligand 1 (PD-L1) immune checkpoint has long been implicated in modeling antitumor immunity; PD-1/PD-L1 axis inhibitors exert their antitumor effects by relieving PD-L1-mediated suppression on tumor-infiltrating T lymphocytes. However, recent st...

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Detalles Bibliográficos
Autores principales: Vathiotis, Ioannis A., Gomatou, Georgia, Stravopodis, Dimitrios J., Syrigos, Nikolaos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8160779/
https://www.ncbi.nlm.nih.gov/pubmed/34065396
http://dx.doi.org/10.3390/ijms22105383
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author Vathiotis, Ioannis A.
Gomatou, Georgia
Stravopodis, Dimitrios J.
Syrigos, Nikolaos
author_facet Vathiotis, Ioannis A.
Gomatou, Georgia
Stravopodis, Dimitrios J.
Syrigos, Nikolaos
author_sort Vathiotis, Ioannis A.
collection PubMed
description Programmed cell death protein 1 (PD-1)/programmed death-ligand 1 (PD-L1) immune checkpoint has long been implicated in modeling antitumor immunity; PD-1/PD-L1 axis inhibitors exert their antitumor effects by relieving PD-L1-mediated suppression on tumor-infiltrating T lymphocytes. However, recent studies have unveiled a distinct, tumor-intrinsic, potential role for PD-L1. In this review, we focus on tumor-intrinsic PD-L1 signaling and delve into preclinical evidence linking PD-L1 protein expression with features of epithelial-to-mesenchymal transition program, cancer stemness and known oncogenic pathways. We further summarize data from studies supporting the prognostic significance of PD-L1 in different tumor types. We show that PD-L1 may indeed have oncogenic potential and act as a regulator of tumor progression and metastasis.
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spelling pubmed-81607792021-05-29 Programmed Death-Ligand 1 as a Regulator of Tumor Progression and Metastasis Vathiotis, Ioannis A. Gomatou, Georgia Stravopodis, Dimitrios J. Syrigos, Nikolaos Int J Mol Sci Review Programmed cell death protein 1 (PD-1)/programmed death-ligand 1 (PD-L1) immune checkpoint has long been implicated in modeling antitumor immunity; PD-1/PD-L1 axis inhibitors exert their antitumor effects by relieving PD-L1-mediated suppression on tumor-infiltrating T lymphocytes. However, recent studies have unveiled a distinct, tumor-intrinsic, potential role for PD-L1. In this review, we focus on tumor-intrinsic PD-L1 signaling and delve into preclinical evidence linking PD-L1 protein expression with features of epithelial-to-mesenchymal transition program, cancer stemness and known oncogenic pathways. We further summarize data from studies supporting the prognostic significance of PD-L1 in different tumor types. We show that PD-L1 may indeed have oncogenic potential and act as a regulator of tumor progression and metastasis. MDPI 2021-05-20 /pmc/articles/PMC8160779/ /pubmed/34065396 http://dx.doi.org/10.3390/ijms22105383 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Vathiotis, Ioannis A.
Gomatou, Georgia
Stravopodis, Dimitrios J.
Syrigos, Nikolaos
Programmed Death-Ligand 1 as a Regulator of Tumor Progression and Metastasis
title Programmed Death-Ligand 1 as a Regulator of Tumor Progression and Metastasis
title_full Programmed Death-Ligand 1 as a Regulator of Tumor Progression and Metastasis
title_fullStr Programmed Death-Ligand 1 as a Regulator of Tumor Progression and Metastasis
title_full_unstemmed Programmed Death-Ligand 1 as a Regulator of Tumor Progression and Metastasis
title_short Programmed Death-Ligand 1 as a Regulator of Tumor Progression and Metastasis
title_sort programmed death-ligand 1 as a regulator of tumor progression and metastasis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8160779/
https://www.ncbi.nlm.nih.gov/pubmed/34065396
http://dx.doi.org/10.3390/ijms22105383
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