Cargando…

Epigenetic polypharmacology: from combination therapy to multitargeted drugs

The modern drug discovery process has largely focused its attention in the so-called magic bullets, single chemical entities that exhibit high selectivity and potency for a particular target. This approach was based on the assumption that the deregulation of a protein was causally linked to a diseas...

Descripción completa

Detalles Bibliográficos
Autores principales: de Lera, Angel R., Ganesan, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062873/
https://www.ncbi.nlm.nih.gov/pubmed/27752293
http://dx.doi.org/10.1186/s13148-016-0271-9
_version_ 1782459864566464512
author de Lera, Angel R.
Ganesan, A.
author_facet de Lera, Angel R.
Ganesan, A.
author_sort de Lera, Angel R.
collection PubMed
description The modern drug discovery process has largely focused its attention in the so-called magic bullets, single chemical entities that exhibit high selectivity and potency for a particular target. This approach was based on the assumption that the deregulation of a protein was causally linked to a disease state, and the pharmacological intervention through inhibition of the deregulated target was able to restore normal cell function. However, the use of cocktails or multicomponent drugs to address several targets simultaneously is also popular to treat multifactorial diseases such as cancer and neurological disorders. We review the state of the art with such combinations that have an epigenetic target as one of their mechanisms of action. Epigenetic drug discovery is a rapidly advancing field, and drugs targeting epigenetic enzymes are in the clinic for the treatment of hematological cancers. Approved and experimental epigenetic drugs are undergoing clinical trials in combination with other therapeutic agents via fused or linked pharmacophores in order to benefit from synergistic effects of polypharmacology. In addition, ligands are being discovered which, as single chemical entities, are able to modulate multiple epigenetic targets simultaneously (multitarget epigenetic drugs). These multiple ligands should in principle have a lower risk of drug-drug interactions and drug resistance compared to cocktails or multicomponent drugs. This new generation may rival the so-called magic bullets in the treatment of diseases that arise as a consequence of the deregulation of multiple signaling pathways provided the challenge of optimization of the activities shown by the pharmacophores with the different targets is addressed.
format Online
Article
Text
id pubmed-5062873
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-50628732016-10-17 Epigenetic polypharmacology: from combination therapy to multitargeted drugs de Lera, Angel R. Ganesan, A. Clin Epigenetics Review The modern drug discovery process has largely focused its attention in the so-called magic bullets, single chemical entities that exhibit high selectivity and potency for a particular target. This approach was based on the assumption that the deregulation of a protein was causally linked to a disease state, and the pharmacological intervention through inhibition of the deregulated target was able to restore normal cell function. However, the use of cocktails or multicomponent drugs to address several targets simultaneously is also popular to treat multifactorial diseases such as cancer and neurological disorders. We review the state of the art with such combinations that have an epigenetic target as one of their mechanisms of action. Epigenetic drug discovery is a rapidly advancing field, and drugs targeting epigenetic enzymes are in the clinic for the treatment of hematological cancers. Approved and experimental epigenetic drugs are undergoing clinical trials in combination with other therapeutic agents via fused or linked pharmacophores in order to benefit from synergistic effects of polypharmacology. In addition, ligands are being discovered which, as single chemical entities, are able to modulate multiple epigenetic targets simultaneously (multitarget epigenetic drugs). These multiple ligands should in principle have a lower risk of drug-drug interactions and drug resistance compared to cocktails or multicomponent drugs. This new generation may rival the so-called magic bullets in the treatment of diseases that arise as a consequence of the deregulation of multiple signaling pathways provided the challenge of optimization of the activities shown by the pharmacophores with the different targets is addressed. BioMed Central 2016-10-12 /pmc/articles/PMC5062873/ /pubmed/27752293 http://dx.doi.org/10.1186/s13148-016-0271-9 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
de Lera, Angel R.
Ganesan, A.
Epigenetic polypharmacology: from combination therapy to multitargeted drugs
title Epigenetic polypharmacology: from combination therapy to multitargeted drugs
title_full Epigenetic polypharmacology: from combination therapy to multitargeted drugs
title_fullStr Epigenetic polypharmacology: from combination therapy to multitargeted drugs
title_full_unstemmed Epigenetic polypharmacology: from combination therapy to multitargeted drugs
title_short Epigenetic polypharmacology: from combination therapy to multitargeted drugs
title_sort epigenetic polypharmacology: from combination therapy to multitargeted drugs
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062873/
https://www.ncbi.nlm.nih.gov/pubmed/27752293
http://dx.doi.org/10.1186/s13148-016-0271-9
work_keys_str_mv AT deleraangelr epigeneticpolypharmacologyfromcombinationtherapytomultitargeteddrugs
AT ganesana epigeneticpolypharmacologyfromcombinationtherapytomultitargeteddrugs