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Targeting CDK4/6 for Anticancer Therapy

Cyclin-dependent kinase 4/6 (CDK4/6) are key regulators of the cell cycle and are deemed as critical therapeutic targets of multiple cancers. Various approaches have been applied to silence CDK4/6 at different levels, i.e., CRISPR to knock out at the DNA level, siRNA to inhibit translation, and drug...

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Detalles Bibliográficos
Autores principales: Qi, Jiating, Ouyang, Zhuqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945444/
https://www.ncbi.nlm.nih.gov/pubmed/35327487
http://dx.doi.org/10.3390/biomedicines10030685
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author Qi, Jiating
Ouyang, Zhuqing
author_facet Qi, Jiating
Ouyang, Zhuqing
author_sort Qi, Jiating
collection PubMed
description Cyclin-dependent kinase 4/6 (CDK4/6) are key regulators of the cell cycle and are deemed as critical therapeutic targets of multiple cancers. Various approaches have been applied to silence CDK4/6 at different levels, i.e., CRISPR to knock out at the DNA level, siRNA to inhibit translation, and drugs that target the protein of interest. Here we summarize the current status in this field, highlighting the mechanisms of small molecular inhibitors treatment and drug resistance. We describe approaches to combat drug resistance, including combination therapy and PROTACs drugs that degrade the kinases. Finally, critical issues and perspectives in the field are outlined.
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spelling pubmed-89454442022-03-25 Targeting CDK4/6 for Anticancer Therapy Qi, Jiating Ouyang, Zhuqing Biomedicines Review Cyclin-dependent kinase 4/6 (CDK4/6) are key regulators of the cell cycle and are deemed as critical therapeutic targets of multiple cancers. Various approaches have been applied to silence CDK4/6 at different levels, i.e., CRISPR to knock out at the DNA level, siRNA to inhibit translation, and drugs that target the protein of interest. Here we summarize the current status in this field, highlighting the mechanisms of small molecular inhibitors treatment and drug resistance. We describe approaches to combat drug resistance, including combination therapy and PROTACs drugs that degrade the kinases. Finally, critical issues and perspectives in the field are outlined. MDPI 2022-03-16 /pmc/articles/PMC8945444/ /pubmed/35327487 http://dx.doi.org/10.3390/biomedicines10030685 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Qi, Jiating
Ouyang, Zhuqing
Targeting CDK4/6 for Anticancer Therapy
title Targeting CDK4/6 for Anticancer Therapy
title_full Targeting CDK4/6 for Anticancer Therapy
title_fullStr Targeting CDK4/6 for Anticancer Therapy
title_full_unstemmed Targeting CDK4/6 for Anticancer Therapy
title_short Targeting CDK4/6 for Anticancer Therapy
title_sort targeting cdk4/6 for anticancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8945444/
https://www.ncbi.nlm.nih.gov/pubmed/35327487
http://dx.doi.org/10.3390/biomedicines10030685
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