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HDAC Inhibition to Prime Immune Checkpoint Inhibitors

SIMPLE SUMMARY: Immunotherapy has made a breakthrough in medical oncology with the approval of several immune checkpoint inhibitors in multiple cancer types. Since only a minority of patients experience a durable response with these agents, combination strategies and novel immunotherapy drugs were d...

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Autores principales: Borcoman, Edith, Kamal, Maud, Marret, Grégoire, Dupain, Celia, Castel-Ajgal, Zahra, Le Tourneau, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750966/
https://www.ncbi.nlm.nih.gov/pubmed/35008230
http://dx.doi.org/10.3390/cancers14010066
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author Borcoman, Edith
Kamal, Maud
Marret, Grégoire
Dupain, Celia
Castel-Ajgal, Zahra
Le Tourneau, Christophe
author_facet Borcoman, Edith
Kamal, Maud
Marret, Grégoire
Dupain, Celia
Castel-Ajgal, Zahra
Le Tourneau, Christophe
author_sort Borcoman, Edith
collection PubMed
description SIMPLE SUMMARY: Immunotherapy has made a breakthrough in medical oncology with the approval of several immune checkpoint inhibitors in multiple cancer types. Since only a minority of patients experience a durable response with these agents, combination strategies and novel immunotherapy drugs were developed to further counteract tumor immune escape. Epigenetic regulations can be altered in oncogenesis, favoring tumor progression. The development of epidrugs has allowed for successfully targeting these altered epigenetic patterns in lymphoma and leukemia patients. It has been recently shown that epigenetic alterations can also play a key role in tumor immune escape. Epidrugs, like HDAC inhibitors, can prime the anti-tumor immune response, therefore constituting interesting partners to develop combination strategies with immunotherapy agents. ABSTRACT: Immunotherapy has made a breakthrough in medical oncology with the approval of several immune checkpoint inhibitors in clinical routine, improving overall survival of advanced cancer patients with refractory disease. However only a minority of patients experience a durable response with these agents, which has led to the development of combination strategies and novel immunotherapy drugs to further counteract tumor immune escape. Epigenetic regulations can be altered in oncogenesis, favoring tumor progression. The development of epidrugs has allowed targeting successfully these altered epigenetic patterns in lymphoma and leukemia patients. It has been recently shown that epigenetic alterations can also play a key role in tumor immune escape. Epidrugs, like HDAC inhibitors, can prime the anti-tumor immune response, therefore constituting interesting partners to develop combination strategies with immunotherapy agents. In this review, we will discuss epigenetic regulations involved in oncogenesis and immune escape and describe the clinical development of combining HDAC inhibitors with immunotherapies.
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spelling pubmed-87509662022-01-12 HDAC Inhibition to Prime Immune Checkpoint Inhibitors Borcoman, Edith Kamal, Maud Marret, Grégoire Dupain, Celia Castel-Ajgal, Zahra Le Tourneau, Christophe Cancers (Basel) Review SIMPLE SUMMARY: Immunotherapy has made a breakthrough in medical oncology with the approval of several immune checkpoint inhibitors in multiple cancer types. Since only a minority of patients experience a durable response with these agents, combination strategies and novel immunotherapy drugs were developed to further counteract tumor immune escape. Epigenetic regulations can be altered in oncogenesis, favoring tumor progression. The development of epidrugs has allowed for successfully targeting these altered epigenetic patterns in lymphoma and leukemia patients. It has been recently shown that epigenetic alterations can also play a key role in tumor immune escape. Epidrugs, like HDAC inhibitors, can prime the anti-tumor immune response, therefore constituting interesting partners to develop combination strategies with immunotherapy agents. ABSTRACT: Immunotherapy has made a breakthrough in medical oncology with the approval of several immune checkpoint inhibitors in clinical routine, improving overall survival of advanced cancer patients with refractory disease. However only a minority of patients experience a durable response with these agents, which has led to the development of combination strategies and novel immunotherapy drugs to further counteract tumor immune escape. Epigenetic regulations can be altered in oncogenesis, favoring tumor progression. The development of epidrugs has allowed targeting successfully these altered epigenetic patterns in lymphoma and leukemia patients. It has been recently shown that epigenetic alterations can also play a key role in tumor immune escape. Epidrugs, like HDAC inhibitors, can prime the anti-tumor immune response, therefore constituting interesting partners to develop combination strategies with immunotherapy agents. In this review, we will discuss epigenetic regulations involved in oncogenesis and immune escape and describe the clinical development of combining HDAC inhibitors with immunotherapies. MDPI 2021-12-23 /pmc/articles/PMC8750966/ /pubmed/35008230 http://dx.doi.org/10.3390/cancers14010066 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
Borcoman, Edith
Kamal, Maud
Marret, Grégoire
Dupain, Celia
Castel-Ajgal, Zahra
Le Tourneau, Christophe
HDAC Inhibition to Prime Immune Checkpoint Inhibitors
title HDAC Inhibition to Prime Immune Checkpoint Inhibitors
title_full HDAC Inhibition to Prime Immune Checkpoint Inhibitors
title_fullStr HDAC Inhibition to Prime Immune Checkpoint Inhibitors
title_full_unstemmed HDAC Inhibition to Prime Immune Checkpoint Inhibitors
title_short HDAC Inhibition to Prime Immune Checkpoint Inhibitors
title_sort hdac inhibition to prime immune checkpoint inhibitors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750966/
https://www.ncbi.nlm.nih.gov/pubmed/35008230
http://dx.doi.org/10.3390/cancers14010066
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