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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-8945444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT qijiating targetingcdk46foranticancertherapy AT ouyangzhuqing targetingcdk46foranticancertherapy |