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Targeting Cullin-RING E3 Ubiquitin Ligase 4 by Small Molecule Modulators

Cullin-RING E3 ubiquitin ligase 4 (CRL4) plays an essential role in cell cycle progression. Recent efforts using high throughput screening and follow up hit-to-lead studies have led to identification of small molecules 33-11 and KH-4-43 that inhibit E3 CRL4’s core ligase complex and exhibit anticanc...

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Detalles Bibliográficos
Autores principales: Wu, Kenneth, Hopkins, Benjamin D., Sanchez, Roberto, DeVita, Robert J., Pan, Zhen-Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486283/
https://www.ncbi.nlm.nih.gov/pubmed/34604860
http://dx.doi.org/10.33696/Signaling.2.051
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author Wu, Kenneth
Hopkins, Benjamin D.
Sanchez, Roberto
DeVita, Robert J.
Pan, Zhen-Qiang
author_facet Wu, Kenneth
Hopkins, Benjamin D.
Sanchez, Roberto
DeVita, Robert J.
Pan, Zhen-Qiang
author_sort Wu, Kenneth
collection PubMed
description Cullin-RING E3 ubiquitin ligase 4 (CRL4) plays an essential role in cell cycle progression. Recent efforts using high throughput screening and follow up hit-to-lead studies have led to identification of small molecules 33-11 and KH-4-43 that inhibit E3 CRL4’s core ligase complex and exhibit anticancer potential. This review provides: 1) an updated perspective of E3 CRL4, including structural organization, major substrate targets and role in cancer; 2) a discussion of the challenges and strategies for finding the CRL inhibitor; and 3) a summary of the properties of the identified CRL4 inhibitors as well as a perspective on their potential utility to probe CRL4 biology and act as therapeutic agents.
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spelling pubmed-84862832021-10-01 Targeting Cullin-RING E3 Ubiquitin Ligase 4 by Small Molecule Modulators Wu, Kenneth Hopkins, Benjamin D. Sanchez, Roberto DeVita, Robert J. Pan, Zhen-Qiang J Cell Signal Article Cullin-RING E3 ubiquitin ligase 4 (CRL4) plays an essential role in cell cycle progression. Recent efforts using high throughput screening and follow up hit-to-lead studies have led to identification of small molecules 33-11 and KH-4-43 that inhibit E3 CRL4’s core ligase complex and exhibit anticancer potential. This review provides: 1) an updated perspective of E3 CRL4, including structural organization, major substrate targets and role in cancer; 2) a discussion of the challenges and strategies for finding the CRL inhibitor; and 3) a summary of the properties of the identified CRL4 inhibitors as well as a perspective on their potential utility to probe CRL4 biology and act as therapeutic agents. 2021 /pmc/articles/PMC8486283/ /pubmed/34604860 http://dx.doi.org/10.33696/Signaling.2.051 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Wu, Kenneth
Hopkins, Benjamin D.
Sanchez, Roberto
DeVita, Robert J.
Pan, Zhen-Qiang
Targeting Cullin-RING E3 Ubiquitin Ligase 4 by Small Molecule Modulators
title Targeting Cullin-RING E3 Ubiquitin Ligase 4 by Small Molecule Modulators
title_full Targeting Cullin-RING E3 Ubiquitin Ligase 4 by Small Molecule Modulators
title_fullStr Targeting Cullin-RING E3 Ubiquitin Ligase 4 by Small Molecule Modulators
title_full_unstemmed Targeting Cullin-RING E3 Ubiquitin Ligase 4 by Small Molecule Modulators
title_short Targeting Cullin-RING E3 Ubiquitin Ligase 4 by Small Molecule Modulators
title_sort targeting cullin-ring e3 ubiquitin ligase 4 by small molecule modulators
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486283/
https://www.ncbi.nlm.nih.gov/pubmed/34604860
http://dx.doi.org/10.33696/Signaling.2.051
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