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Targets in Epigenetics: Inhibiting the Methyl Writers of the Histone Code

Growing evidence suggests that protein lysine methyltransferases (PKMTs) and protein arginine methyltransferases (PRMTs) are associated with the development of various human diseases, including cancer, inflammation, and psychiatric disorders. Given the significant role of these proteins in human dis...

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Detalles Bibliográficos
Autores principales: Yost, Julianne M, Korboukh, Ilia, Liu, Feng, Gao, Cen, Jin, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3178896/
https://www.ncbi.nlm.nih.gov/pubmed/21966347
http://dx.doi.org/10.2174/1875397301005010072
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author Yost, Julianne M
Korboukh, Ilia
Liu, Feng
Gao, Cen
Jin, Jian
author_facet Yost, Julianne M
Korboukh, Ilia
Liu, Feng
Gao, Cen
Jin, Jian
author_sort Yost, Julianne M
collection PubMed
description Growing evidence suggests that protein lysine methyltransferases (PKMTs) and protein arginine methyltransferases (PRMTs) are associated with the development of various human diseases, including cancer, inflammation, and psychiatric disorders. Given the significant role of these proteins in human disease, efforts to discover selective small-molecule inhibitors of these enzymes are quickly gaining momentum. In this review, we focus on the recent progress in the discovery of selective PKMT and PRMT inhibitors. A future perspective on developing methyltransferase inhibitors is also offered.
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spelling pubmed-31788962011-09-30 Targets in Epigenetics: Inhibiting the Methyl Writers of the Histone Code Yost, Julianne M Korboukh, Ilia Liu, Feng Gao, Cen Jin, Jian Curr Chem Genomics Article Growing evidence suggests that protein lysine methyltransferases (PKMTs) and protein arginine methyltransferases (PRMTs) are associated with the development of various human diseases, including cancer, inflammation, and psychiatric disorders. Given the significant role of these proteins in human disease, efforts to discover selective small-molecule inhibitors of these enzymes are quickly gaining momentum. In this review, we focus on the recent progress in the discovery of selective PKMT and PRMT inhibitors. A future perspective on developing methyltransferase inhibitors is also offered. Bentham Open 2011-08-22 /pmc/articles/PMC3178896/ /pubmed/21966347 http://dx.doi.org/10.2174/1875397301005010072 Text en © Yost et al.; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Yost, Julianne M
Korboukh, Ilia
Liu, Feng
Gao, Cen
Jin, Jian
Targets in Epigenetics: Inhibiting the Methyl Writers of the Histone Code
title Targets in Epigenetics: Inhibiting the Methyl Writers of the Histone Code
title_full Targets in Epigenetics: Inhibiting the Methyl Writers of the Histone Code
title_fullStr Targets in Epigenetics: Inhibiting the Methyl Writers of the Histone Code
title_full_unstemmed Targets in Epigenetics: Inhibiting the Methyl Writers of the Histone Code
title_short Targets in Epigenetics: Inhibiting the Methyl Writers of the Histone Code
title_sort targets in epigenetics: inhibiting the methyl writers of the histone code
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3178896/
https://www.ncbi.nlm.nih.gov/pubmed/21966347
http://dx.doi.org/10.2174/1875397301005010072
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