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A New Functional Screening Platform Identifies Colistin Sulfate as an Enhancer of Natural Killer Cell Cytotoxicity

SIMPLE SUMMARY: The use of small compounds in cancer immunotherapy has been limited so far. Her we screen for drugs that enhanced the ability of immune cells to kill tumor cells and identified the molecule Colistin Sulfate as a booster of immune activity. ABSTRACT: Due to their crucial role in tumor...

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Autores principales: Cortés-Kaplan, Serena, Kurdieh, Reem, Hasim, Mohamed S., Kaczmarek, Shelby, Taha, Zaid, Maznyi, Glib, McComb, Scott, Lee, Seung-Hwan, Diallo, Jean-Simon, Ardolino, Michele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221353/
https://www.ncbi.nlm.nih.gov/pubmed/35740500
http://dx.doi.org/10.3390/cancers14122832
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author Cortés-Kaplan, Serena
Kurdieh, Reem
Hasim, Mohamed S.
Kaczmarek, Shelby
Taha, Zaid
Maznyi, Glib
McComb, Scott
Lee, Seung-Hwan
Diallo, Jean-Simon
Ardolino, Michele
author_facet Cortés-Kaplan, Serena
Kurdieh, Reem
Hasim, Mohamed S.
Kaczmarek, Shelby
Taha, Zaid
Maznyi, Glib
McComb, Scott
Lee, Seung-Hwan
Diallo, Jean-Simon
Ardolino, Michele
author_sort Cortés-Kaplan, Serena
collection PubMed
description SIMPLE SUMMARY: The use of small compounds in cancer immunotherapy has been limited so far. Her we screen for drugs that enhanced the ability of immune cells to kill tumor cells and identified the molecule Colistin Sulfate as a booster of immune activity. ABSTRACT: Due to their crucial role in tumor immunity, NK cells have quickly became a prime target for immunotherapies, with the adoptive transfer of NK cells and the use of NK cell engagers quickly moving to the clinical stage. On the other hand, only a few studies have focused on small molecule drugs capable of unleashing NK cells against cancer. In this context, repurposing small molecules is an attractive strategy to identify new immunotherapies from already approved drugs. Here, we developed a new platform to screen small molecule compounds based on a high-throughput luciferase-release cytotoxicity assay. We tested 1200 FDA approved drugs from the Prestwick Chemical Library, to identify compounds that increase NK cells’ cytotoxic potential. We found that the antibiotic colistin sulfate increased the cytotoxicity of human NK cells towards cancer cells. The effect of colistin was short lived and was not observed when NK cells were pretreated with the drug, showing how NK cell activity was potentiated only when the compound was present at the time of recognition of cancer cells. Further studies are needed to uncover the mechanism of action and the pre-clinical efficacy of colistin sulfate in mouse cancer models.
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spelling pubmed-92213532022-06-24 A New Functional Screening Platform Identifies Colistin Sulfate as an Enhancer of Natural Killer Cell Cytotoxicity Cortés-Kaplan, Serena Kurdieh, Reem Hasim, Mohamed S. Kaczmarek, Shelby Taha, Zaid Maznyi, Glib McComb, Scott Lee, Seung-Hwan Diallo, Jean-Simon Ardolino, Michele Cancers (Basel) Article SIMPLE SUMMARY: The use of small compounds in cancer immunotherapy has been limited so far. Her we screen for drugs that enhanced the ability of immune cells to kill tumor cells and identified the molecule Colistin Sulfate as a booster of immune activity. ABSTRACT: Due to their crucial role in tumor immunity, NK cells have quickly became a prime target for immunotherapies, with the adoptive transfer of NK cells and the use of NK cell engagers quickly moving to the clinical stage. On the other hand, only a few studies have focused on small molecule drugs capable of unleashing NK cells against cancer. In this context, repurposing small molecules is an attractive strategy to identify new immunotherapies from already approved drugs. Here, we developed a new platform to screen small molecule compounds based on a high-throughput luciferase-release cytotoxicity assay. We tested 1200 FDA approved drugs from the Prestwick Chemical Library, to identify compounds that increase NK cells’ cytotoxic potential. We found that the antibiotic colistin sulfate increased the cytotoxicity of human NK cells towards cancer cells. The effect of colistin was short lived and was not observed when NK cells were pretreated with the drug, showing how NK cell activity was potentiated only when the compound was present at the time of recognition of cancer cells. Further studies are needed to uncover the mechanism of action and the pre-clinical efficacy of colistin sulfate in mouse cancer models. MDPI 2022-06-08 /pmc/articles/PMC9221353/ /pubmed/35740500 http://dx.doi.org/10.3390/cancers14122832 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 Article
Cortés-Kaplan, Serena
Kurdieh, Reem
Hasim, Mohamed S.
Kaczmarek, Shelby
Taha, Zaid
Maznyi, Glib
McComb, Scott
Lee, Seung-Hwan
Diallo, Jean-Simon
Ardolino, Michele
A New Functional Screening Platform Identifies Colistin Sulfate as an Enhancer of Natural Killer Cell Cytotoxicity
title A New Functional Screening Platform Identifies Colistin Sulfate as an Enhancer of Natural Killer Cell Cytotoxicity
title_full A New Functional Screening Platform Identifies Colistin Sulfate as an Enhancer of Natural Killer Cell Cytotoxicity
title_fullStr A New Functional Screening Platform Identifies Colistin Sulfate as an Enhancer of Natural Killer Cell Cytotoxicity
title_full_unstemmed A New Functional Screening Platform Identifies Colistin Sulfate as an Enhancer of Natural Killer Cell Cytotoxicity
title_short A New Functional Screening Platform Identifies Colistin Sulfate as an Enhancer of Natural Killer Cell Cytotoxicity
title_sort new functional screening platform identifies colistin sulfate as an enhancer of natural killer cell cytotoxicity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221353/
https://www.ncbi.nlm.nih.gov/pubmed/35740500
http://dx.doi.org/10.3390/cancers14122832
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