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Natural Killer Cells: Tumor Surveillance and Signaling

Natural killer (NK) cells play a pivotal role in cancer immunotherapy due to their innate ability to detect and kill tumorigenic cells. The decision to kill is determined by the expression of a myriad of activating and inhibitory receptors on the NK cell surface. Cell-to-cell engagement results in e...

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Detalles Bibliográficos
Autores principales: Meza Guzman, Lizeth G., Keating, Narelle, Nicholson, Sandra E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226588/
https://www.ncbi.nlm.nih.gov/pubmed/32290478
http://dx.doi.org/10.3390/cancers12040952
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author Meza Guzman, Lizeth G.
Keating, Narelle
Nicholson, Sandra E.
author_facet Meza Guzman, Lizeth G.
Keating, Narelle
Nicholson, Sandra E.
author_sort Meza Guzman, Lizeth G.
collection PubMed
description Natural killer (NK) cells play a pivotal role in cancer immunotherapy due to their innate ability to detect and kill tumorigenic cells. The decision to kill is determined by the expression of a myriad of activating and inhibitory receptors on the NK cell surface. Cell-to-cell engagement results in either self-tolerance or a cytotoxic response, governed by a fine balance between the signaling cascades downstream of the activating and inhibitory receptors. To evade a cytotoxic immune response, tumor cells can modulate the surface expression of receptor ligands and additionally, alter the conditions in the tumor microenvironment (TME), tilting the scales toward a suppressed cytotoxic NK response. To fully harness the killing power of NK cells for clinical benefit, we need to understand what defines the threshold for activation and what is required to break tolerance. This review will focus on the intracellular signaling pathways activated or suppressed in NK cells and the roles signaling intermediates play during an NK cytotoxic response.
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spelling pubmed-72265882020-05-18 Natural Killer Cells: Tumor Surveillance and Signaling Meza Guzman, Lizeth G. Keating, Narelle Nicholson, Sandra E. Cancers (Basel) Review Natural killer (NK) cells play a pivotal role in cancer immunotherapy due to their innate ability to detect and kill tumorigenic cells. The decision to kill is determined by the expression of a myriad of activating and inhibitory receptors on the NK cell surface. Cell-to-cell engagement results in either self-tolerance or a cytotoxic response, governed by a fine balance between the signaling cascades downstream of the activating and inhibitory receptors. To evade a cytotoxic immune response, tumor cells can modulate the surface expression of receptor ligands and additionally, alter the conditions in the tumor microenvironment (TME), tilting the scales toward a suppressed cytotoxic NK response. To fully harness the killing power of NK cells for clinical benefit, we need to understand what defines the threshold for activation and what is required to break tolerance. This review will focus on the intracellular signaling pathways activated or suppressed in NK cells and the roles signaling intermediates play during an NK cytotoxic response. MDPI 2020-04-11 /pmc/articles/PMC7226588/ /pubmed/32290478 http://dx.doi.org/10.3390/cancers12040952 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Meza Guzman, Lizeth G.
Keating, Narelle
Nicholson, Sandra E.
Natural Killer Cells: Tumor Surveillance and Signaling
title Natural Killer Cells: Tumor Surveillance and Signaling
title_full Natural Killer Cells: Tumor Surveillance and Signaling
title_fullStr Natural Killer Cells: Tumor Surveillance and Signaling
title_full_unstemmed Natural Killer Cells: Tumor Surveillance and Signaling
title_short Natural Killer Cells: Tumor Surveillance and Signaling
title_sort natural killer cells: tumor surveillance and signaling
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226588/
https://www.ncbi.nlm.nih.gov/pubmed/32290478
http://dx.doi.org/10.3390/cancers12040952
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