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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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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. |
format | Online Article Text |
id | pubmed-6356452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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