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Expanding the Structural Diversity of DNA Methyltransferase Inhibitors
Inhibitors of DNA methyltransferases (DNMTs) are attractive compounds for epigenetic drug discovery. They are also chemical tools to understand the biochemistry of epigenetic processes. Herein, we report five distinct inhibitors of DNMT1 characterized in enzymatic inhibition assays that did not show...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824300/ https://www.ncbi.nlm.nih.gov/pubmed/33375520 http://dx.doi.org/10.3390/ph14010017 |
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author | Juárez-Mercado, K. Eurídice Prieto-Martínez, Fernando D. Sánchez-Cruz, Norberto Peña-Castillo, Andrea Prada-Gracia, Diego Medina-Franco, José L. |
author_facet | Juárez-Mercado, K. Eurídice Prieto-Martínez, Fernando D. Sánchez-Cruz, Norberto Peña-Castillo, Andrea Prada-Gracia, Diego Medina-Franco, José L. |
author_sort | Juárez-Mercado, K. Eurídice |
collection | PubMed |
description | Inhibitors of DNA methyltransferases (DNMTs) are attractive compounds for epigenetic drug discovery. They are also chemical tools to understand the biochemistry of epigenetic processes. Herein, we report five distinct inhibitors of DNMT1 characterized in enzymatic inhibition assays that did not show activity with DNMT3B. It was concluded that the dietary component theaflavin is an inhibitor of DNMT1. Two additional novel inhibitors of DNMT1 are the approved drugs glyburide and panobinostat. The DNMT1 enzymatic inhibitory activity of panobinostat, a known pan inhibitor of histone deacetylases, agrees with experimental reports of its ability to reduce DNMT1 activity in liver cancer cell lines. Molecular docking of the active compounds with DNMT1, and re-scoring with the recently developed extended connectivity interaction features approach, led to an excellent agreement between the experimental IC(50) values and docking scores. |
format | Online Article Text |
id | pubmed-7824300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78243002021-01-24 Expanding the Structural Diversity of DNA Methyltransferase Inhibitors Juárez-Mercado, K. Eurídice Prieto-Martínez, Fernando D. Sánchez-Cruz, Norberto Peña-Castillo, Andrea Prada-Gracia, Diego Medina-Franco, José L. Pharmaceuticals (Basel) Article Inhibitors of DNA methyltransferases (DNMTs) are attractive compounds for epigenetic drug discovery. They are also chemical tools to understand the biochemistry of epigenetic processes. Herein, we report five distinct inhibitors of DNMT1 characterized in enzymatic inhibition assays that did not show activity with DNMT3B. It was concluded that the dietary component theaflavin is an inhibitor of DNMT1. Two additional novel inhibitors of DNMT1 are the approved drugs glyburide and panobinostat. The DNMT1 enzymatic inhibitory activity of panobinostat, a known pan inhibitor of histone deacetylases, agrees with experimental reports of its ability to reduce DNMT1 activity in liver cancer cell lines. Molecular docking of the active compounds with DNMT1, and re-scoring with the recently developed extended connectivity interaction features approach, led to an excellent agreement between the experimental IC(50) values and docking scores. MDPI 2020-12-27 /pmc/articles/PMC7824300/ /pubmed/33375520 http://dx.doi.org/10.3390/ph14010017 Text en © 2020 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 | Article Juárez-Mercado, K. Eurídice Prieto-Martínez, Fernando D. Sánchez-Cruz, Norberto Peña-Castillo, Andrea Prada-Gracia, Diego Medina-Franco, José L. Expanding the Structural Diversity of DNA Methyltransferase Inhibitors |
title | Expanding the Structural Diversity of DNA Methyltransferase Inhibitors |
title_full | Expanding the Structural Diversity of DNA Methyltransferase Inhibitors |
title_fullStr | Expanding the Structural Diversity of DNA Methyltransferase Inhibitors |
title_full_unstemmed | Expanding the Structural Diversity of DNA Methyltransferase Inhibitors |
title_short | Expanding the Structural Diversity of DNA Methyltransferase Inhibitors |
title_sort | expanding the structural diversity of dna methyltransferase inhibitors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824300/ https://www.ncbi.nlm.nih.gov/pubmed/33375520 http://dx.doi.org/10.3390/ph14010017 |
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