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Highlights in USP7 inhibitors for cancer treatment
Ubiquitin-specific protease 7 (USP7) is a member of one of the most largely studied families of deubiquitylating enzymes. It plays a key role modulating the levels of multiple proteins, including tumor suppressors, transcription factors, epigenetic modulators, DNA repair proteins, and regulators of...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520255/ https://www.ncbi.nlm.nih.gov/pubmed/36186590 http://dx.doi.org/10.3389/fchem.2022.1005727 |
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author | Oliveira, Rita I. Guedes, Romina A. Salvador, Jorge A. R. |
author_facet | Oliveira, Rita I. Guedes, Romina A. Salvador, Jorge A. R. |
author_sort | Oliveira, Rita I. |
collection | PubMed |
description | Ubiquitin-specific protease 7 (USP7) is a member of one of the most largely studied families of deubiquitylating enzymes. It plays a key role modulating the levels of multiple proteins, including tumor suppressors, transcription factors, epigenetic modulators, DNA repair proteins, and regulators of the immune response. The abnormal expression of USP7 is found in various malignant tumors and a high expression signature generally indicates poor tumor prognosis. This suggests USP7 as a promising prognostic and druggable target for cancer therapy. Nonetheless, no approved drugs targeting USP7 have already entered clinical trials. Therefore, the development of potent and selective USP7 inhibitors still requires intensive research and development efforts before the pre-clinical benefits translate into the clinic. This mini review systematically summarizes the role of USP7 as a drug target for cancer therapeutics, as well as the scaffolds, activities, and binding modes of some of the most representative small molecule USP7 inhibitors reported in the scientific literature. To wind up, development challenges and potential combination therapies using USP7 inhibitors for less tractable tumors are also disclosed. |
format | Online Article Text |
id | pubmed-9520255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95202552022-09-30 Highlights in USP7 inhibitors for cancer treatment Oliveira, Rita I. Guedes, Romina A. Salvador, Jorge A. R. Front Chem Chemistry Ubiquitin-specific protease 7 (USP7) is a member of one of the most largely studied families of deubiquitylating enzymes. It plays a key role modulating the levels of multiple proteins, including tumor suppressors, transcription factors, epigenetic modulators, DNA repair proteins, and regulators of the immune response. The abnormal expression of USP7 is found in various malignant tumors and a high expression signature generally indicates poor tumor prognosis. This suggests USP7 as a promising prognostic and druggable target for cancer therapy. Nonetheless, no approved drugs targeting USP7 have already entered clinical trials. Therefore, the development of potent and selective USP7 inhibitors still requires intensive research and development efforts before the pre-clinical benefits translate into the clinic. This mini review systematically summarizes the role of USP7 as a drug target for cancer therapeutics, as well as the scaffolds, activities, and binding modes of some of the most representative small molecule USP7 inhibitors reported in the scientific literature. To wind up, development challenges and potential combination therapies using USP7 inhibitors for less tractable tumors are also disclosed. Frontiers Media S.A. 2022-09-15 /pmc/articles/PMC9520255/ /pubmed/36186590 http://dx.doi.org/10.3389/fchem.2022.1005727 Text en Copyright © 2022 Oliveira, Guedes and Salvador. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Oliveira, Rita I. Guedes, Romina A. Salvador, Jorge A. R. Highlights in USP7 inhibitors for cancer treatment |
title | Highlights in USP7 inhibitors for cancer treatment |
title_full | Highlights in USP7 inhibitors for cancer treatment |
title_fullStr | Highlights in USP7 inhibitors for cancer treatment |
title_full_unstemmed | Highlights in USP7 inhibitors for cancer treatment |
title_short | Highlights in USP7 inhibitors for cancer treatment |
title_sort | highlights in usp7 inhibitors for cancer treatment |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520255/ https://www.ncbi.nlm.nih.gov/pubmed/36186590 http://dx.doi.org/10.3389/fchem.2022.1005727 |
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