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Inhibitors of Protein Methyltransferases and Demethylases
[Image: see text] Post-translational modifications of histones by protein methyltransferases (PMTs) and histone demethylases (KDMs) play an important role in the regulation of gene expression and transcription and are implicated in cancer and many other diseases. Many of these enzymes also target va...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610952/ https://www.ncbi.nlm.nih.gov/pubmed/28338320 http://dx.doi.org/10.1021/acs.chemrev.6b00801 |
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author | Kaniskan, H. Ümit Martini, Michael L. Jin, Jian |
author_facet | Kaniskan, H. Ümit Martini, Michael L. Jin, Jian |
author_sort | Kaniskan, H. Ümit |
collection | PubMed |
description | [Image: see text] Post-translational modifications of histones by protein methyltransferases (PMTs) and histone demethylases (KDMs) play an important role in the regulation of gene expression and transcription and are implicated in cancer and many other diseases. Many of these enzymes also target various nonhistone proteins impacting numerous crucial biological pathways. Given their key biological functions and implications in human diseases, there has been a growing interest in assessing these enzymes as potential therapeutic targets. Consequently, discovering and developing inhibitors of these enzymes has become a very active and fast-growing research area over the past decade. In this review, we cover the discovery, characterization, and biological application of inhibitors of PMTs and KDMs with emphasis on key advancements in the field. We also discuss challenges, opportunities, and future directions in this emerging, exciting research field. |
format | Online Article Text |
id | pubmed-5610952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56109522018-02-20 Inhibitors of Protein Methyltransferases and Demethylases Kaniskan, H. Ümit Martini, Michael L. Jin, Jian Chem Rev [Image: see text] Post-translational modifications of histones by protein methyltransferases (PMTs) and histone demethylases (KDMs) play an important role in the regulation of gene expression and transcription and are implicated in cancer and many other diseases. Many of these enzymes also target various nonhistone proteins impacting numerous crucial biological pathways. Given their key biological functions and implications in human diseases, there has been a growing interest in assessing these enzymes as potential therapeutic targets. Consequently, discovering and developing inhibitors of these enzymes has become a very active and fast-growing research area over the past decade. In this review, we cover the discovery, characterization, and biological application of inhibitors of PMTs and KDMs with emphasis on key advancements in the field. We also discuss challenges, opportunities, and future directions in this emerging, exciting research field. American Chemical Society 2017-03-24 2018-02-14 /pmc/articles/PMC5610952/ /pubmed/28338320 http://dx.doi.org/10.1021/acs.chemrev.6b00801 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Kaniskan, H. Ümit Martini, Michael L. Jin, Jian Inhibitors of Protein Methyltransferases and Demethylases |
title | Inhibitors of Protein Methyltransferases and Demethylases |
title_full | Inhibitors of Protein Methyltransferases and Demethylases |
title_fullStr | Inhibitors of Protein Methyltransferases and Demethylases |
title_full_unstemmed | Inhibitors of Protein Methyltransferases and Demethylases |
title_short | Inhibitors of Protein Methyltransferases and Demethylases |
title_sort | inhibitors of protein methyltransferases and demethylases |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610952/ https://www.ncbi.nlm.nih.gov/pubmed/28338320 http://dx.doi.org/10.1021/acs.chemrev.6b00801 |
work_keys_str_mv | AT kaniskanhumit inhibitorsofproteinmethyltransferasesanddemethylases AT martinimichaell inhibitorsofproteinmethyltransferasesanddemethylases AT jinjian inhibitorsofproteinmethyltransferasesanddemethylases |