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Reading Cancer: Chromatin Readers as Druggable Targets for Cancer Treatment

The epigenetic machinery deputed to control histone post-translational modifications is frequently dysregulated in cancer cells. With epigenetics being naturally reversible, it represents a good target for therapies directed to restore normal gene expression. Since the discovery of Bromodomain and E...

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Detalles Bibliográficos
Autores principales: Mio, Catia, Bulotta, Stefania, Russo, Diego, Damante, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356452/
https://www.ncbi.nlm.nih.gov/pubmed/30634442
http://dx.doi.org/10.3390/cancers11010061
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author Mio, Catia
Bulotta, Stefania
Russo, Diego
Damante, Giuseppe
author_facet Mio, Catia
Bulotta, Stefania
Russo, Diego
Damante, Giuseppe
author_sort Mio, Catia
collection PubMed
description The epigenetic machinery deputed to control histone post-translational modifications is frequently dysregulated in cancer cells. With epigenetics being naturally reversible, it represents a good target for therapies directed to restore normal gene expression. Since the discovery of Bromodomain and Extra Terminal (BET) inhibitors, a great effort has been spent investigating the effects of chromatin readers’ inhibition, specifically the class of proteins assigned to bind acetylated and methylated residues. So far, focused studies have been produced on epigenetic regulation, dissecting a specific class of epigenetic-related proteins or investigating epigenetic therapy in a specific tumor type. In this review, recent steps toward drug discovery on the different classes of chromatin readers have been outlined, highlighting the pros and cons of current therapeutic approaches.
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spelling pubmed-63564522019-02-05 Reading Cancer: Chromatin Readers as Druggable Targets for Cancer Treatment Mio, Catia Bulotta, Stefania Russo, Diego Damante, Giuseppe Cancers (Basel) Review The epigenetic machinery deputed to control histone post-translational modifications is frequently dysregulated in cancer cells. With epigenetics being naturally reversible, it represents a good target for therapies directed to restore normal gene expression. Since the discovery of Bromodomain and Extra Terminal (BET) inhibitors, a great effort has been spent investigating the effects of chromatin readers’ inhibition, specifically the class of proteins assigned to bind acetylated and methylated residues. So far, focused studies have been produced on epigenetic regulation, dissecting a specific class of epigenetic-related proteins or investigating epigenetic therapy in a specific tumor type. In this review, recent steps toward drug discovery on the different classes of chromatin readers have been outlined, highlighting the pros and cons of current therapeutic approaches. MDPI 2019-01-09 /pmc/articles/PMC6356452/ /pubmed/30634442 http://dx.doi.org/10.3390/cancers11010061 Text en © 2019 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
Mio, Catia
Bulotta, Stefania
Russo, Diego
Damante, Giuseppe
Reading Cancer: Chromatin Readers as Druggable Targets for Cancer Treatment
title Reading Cancer: Chromatin Readers as Druggable Targets for Cancer Treatment
title_full Reading Cancer: Chromatin Readers as Druggable Targets for Cancer Treatment
title_fullStr Reading Cancer: Chromatin Readers as Druggable Targets for Cancer Treatment
title_full_unstemmed Reading Cancer: Chromatin Readers as Druggable Targets for Cancer Treatment
title_short Reading Cancer: Chromatin Readers as Druggable Targets for Cancer Treatment
title_sort reading cancer: chromatin readers as druggable targets for cancer treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6356452/
https://www.ncbi.nlm.nih.gov/pubmed/30634442
http://dx.doi.org/10.3390/cancers11010061
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