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Polycomb Repressive Complex 2 Modulation through the Development of EZH2–EED Interaction Inhibitors and EED Binders
[Image: see text] Epigenetics is nowadays a well-accepted area of research. In the last years, tremendous progress was made regarding molecules targeting EZH2, directly or indirectly. Recently tazemetostat hit the market after FDA-approval for the treatment of lymphoma. However, the impairment of EZ...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404197/ https://www.ncbi.nlm.nih.gov/pubmed/34351144 http://dx.doi.org/10.1021/acs.jmedchem.1c00226 |
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author | Tomassi, Stefano Romanelli, Annalisa Zwergel, Clemens Valente, Sergio Mai, Antonello |
author_facet | Tomassi, Stefano Romanelli, Annalisa Zwergel, Clemens Valente, Sergio Mai, Antonello |
author_sort | Tomassi, Stefano |
collection | PubMed |
description | [Image: see text] Epigenetics is nowadays a well-accepted area of research. In the last years, tremendous progress was made regarding molecules targeting EZH2, directly or indirectly. Recently tazemetostat hit the market after FDA-approval for the treatment of lymphoma. However, the impairment of EZH2 activity by orthosteric intervention has proven to be effective only in a limited subset of cancers. Considering the multiproteic nature of the PRC2 complex and the marked dependence of EZH2 functions on the other core subunits such as EED, in recent years, a new targeting approach ascended to prominence. The possibility to cripple the function of the PRC2 complex by interfering with its multimeric integrity fueled the interest in developing EZH2–EED protein–protein interaction and EED inhibitors as indirect modulators of PRC2-dependent methyltransferase activity. In this Perspective, we aim to summarize the latest findings regarding the development and the biological activity of these emerging classes of PRC2 modulators from a medicinal chemist’s viewpoint. |
format | Online Article Text |
id | pubmed-8404197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-84041972021-08-31 Polycomb Repressive Complex 2 Modulation through the Development of EZH2–EED Interaction Inhibitors and EED Binders Tomassi, Stefano Romanelli, Annalisa Zwergel, Clemens Valente, Sergio Mai, Antonello J Med Chem [Image: see text] Epigenetics is nowadays a well-accepted area of research. In the last years, tremendous progress was made regarding molecules targeting EZH2, directly or indirectly. Recently tazemetostat hit the market after FDA-approval for the treatment of lymphoma. However, the impairment of EZH2 activity by orthosteric intervention has proven to be effective only in a limited subset of cancers. Considering the multiproteic nature of the PRC2 complex and the marked dependence of EZH2 functions on the other core subunits such as EED, in recent years, a new targeting approach ascended to prominence. The possibility to cripple the function of the PRC2 complex by interfering with its multimeric integrity fueled the interest in developing EZH2–EED protein–protein interaction and EED inhibitors as indirect modulators of PRC2-dependent methyltransferase activity. In this Perspective, we aim to summarize the latest findings regarding the development and the biological activity of these emerging classes of PRC2 modulators from a medicinal chemist’s viewpoint. American Chemical Society 2021-08-05 2021-08-26 /pmc/articles/PMC8404197/ /pubmed/34351144 http://dx.doi.org/10.1021/acs.jmedchem.1c00226 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Tomassi, Stefano Romanelli, Annalisa Zwergel, Clemens Valente, Sergio Mai, Antonello Polycomb Repressive Complex 2 Modulation through the Development of EZH2–EED Interaction Inhibitors and EED Binders |
title | Polycomb Repressive
Complex 2 Modulation through the
Development of EZH2–EED Interaction Inhibitors and EED Binders |
title_full | Polycomb Repressive
Complex 2 Modulation through the
Development of EZH2–EED Interaction Inhibitors and EED Binders |
title_fullStr | Polycomb Repressive
Complex 2 Modulation through the
Development of EZH2–EED Interaction Inhibitors and EED Binders |
title_full_unstemmed | Polycomb Repressive
Complex 2 Modulation through the
Development of EZH2–EED Interaction Inhibitors and EED Binders |
title_short | Polycomb Repressive
Complex 2 Modulation through the
Development of EZH2–EED Interaction Inhibitors and EED Binders |
title_sort | polycomb repressive
complex 2 modulation through the
development of ezh2–eed interaction inhibitors and eed binders |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404197/ https://www.ncbi.nlm.nih.gov/pubmed/34351144 http://dx.doi.org/10.1021/acs.jmedchem.1c00226 |
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