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Clinical CDK4/6 inhibitors induce selective and immediate dissociation of p21 from cyclin D-CDK4 to inhibit CDK2

Since their discovery as drivers of proliferation, cyclin-dependent kinases (CDKs) have been considered therapeutic targets. Small molecule inhibitors of CDK4/6 are used and tested in clinical trials to treat multiple cancer types. Despite their clinical importance, little is known about how CDK4/6...

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Detalles Bibliográficos
Autores principales: Pack, Lindsey R., Daigh, Leighton H., Chung, Mingyu, Meyer, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184839/
https://www.ncbi.nlm.nih.gov/pubmed/34099663
http://dx.doi.org/10.1038/s41467-021-23612-z