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CD24: A Novel Target for Cancer Immunotherapy

Cluster of differentiation 24 (CD24) is a small, highly glycosylated cell adhesion protein that is normally expressed by immune as well as epithelial, neural, and muscle cells. Tumor CD24 expression has been linked with alterations in several oncogenic signaling pathways. In addition, the CD24/Sigle...

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Autores principales: Panagiotou, Emmanouil, Syrigos, Nikolaos K., Charpidou, Andriani, Kotteas, Elias, Vathiotis, Ioannis A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9409925/
https://www.ncbi.nlm.nih.gov/pubmed/36013184
http://dx.doi.org/10.3390/jpm12081235
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author Panagiotou, Emmanouil
Syrigos, Nikolaos K.
Charpidou, Andriani
Kotteas, Elias
Vathiotis, Ioannis A.
author_facet Panagiotou, Emmanouil
Syrigos, Nikolaos K.
Charpidou, Andriani
Kotteas, Elias
Vathiotis, Ioannis A.
author_sort Panagiotou, Emmanouil
collection PubMed
description Cluster of differentiation 24 (CD24) is a small, highly glycosylated cell adhesion protein that is normally expressed by immune as well as epithelial, neural, and muscle cells. Tumor CD24 expression has been linked with alterations in several oncogenic signaling pathways. In addition, the CD24/Siglec-10 interaction has been implicated in tumor immune evasion, inhibiting macrophage-mediated phagocytosis as well as natural killer (NK) cell cytotoxicity. CD24 blockade has shown promising results in preclinical studies. Although there are limited data on efficacy, monoclonal antibodies against CD24 have demonstrated clinical safety and tolerability in two clinical trials. Other treatment modalities evaluated in the preclinical setting include antibody–drug conjugates and chimeric antigen receptor (CAR) T cell therapy. In this review, we summarize current evidence and future perspectives on CD24 as a potential target for cancer immunotherapy.
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spelling pubmed-94099252022-08-26 CD24: A Novel Target for Cancer Immunotherapy Panagiotou, Emmanouil Syrigos, Nikolaos K. Charpidou, Andriani Kotteas, Elias Vathiotis, Ioannis A. J Pers Med Review Cluster of differentiation 24 (CD24) is a small, highly glycosylated cell adhesion protein that is normally expressed by immune as well as epithelial, neural, and muscle cells. Tumor CD24 expression has been linked with alterations in several oncogenic signaling pathways. In addition, the CD24/Siglec-10 interaction has been implicated in tumor immune evasion, inhibiting macrophage-mediated phagocytosis as well as natural killer (NK) cell cytotoxicity. CD24 blockade has shown promising results in preclinical studies. Although there are limited data on efficacy, monoclonal antibodies against CD24 have demonstrated clinical safety and tolerability in two clinical trials. Other treatment modalities evaluated in the preclinical setting include antibody–drug conjugates and chimeric antigen receptor (CAR) T cell therapy. In this review, we summarize current evidence and future perspectives on CD24 as a potential target for cancer immunotherapy. MDPI 2022-07-28 /pmc/articles/PMC9409925/ /pubmed/36013184 http://dx.doi.org/10.3390/jpm12081235 Text en © 2022 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
Panagiotou, Emmanouil
Syrigos, Nikolaos K.
Charpidou, Andriani
Kotteas, Elias
Vathiotis, Ioannis A.
CD24: A Novel Target for Cancer Immunotherapy
title CD24: A Novel Target for Cancer Immunotherapy
title_full CD24: A Novel Target for Cancer Immunotherapy
title_fullStr CD24: A Novel Target for Cancer Immunotherapy
title_full_unstemmed CD24: A Novel Target for Cancer Immunotherapy
title_short CD24: A Novel Target for Cancer Immunotherapy
title_sort cd24: a novel target for cancer immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9409925/
https://www.ncbi.nlm.nih.gov/pubmed/36013184
http://dx.doi.org/10.3390/jpm12081235
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