Targeting CDK4 and CDK6 in cancer
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Earth and Planetary Sciences,General Environmental Science
Link
https://www.nature.com/articles/s41568-022-00456-3.pdf
Reference263 articles.
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2. Losiewicz, M. D., Carlson, B. A., Kaur, G., Sausville, E. A. & Worland, P. J. Potent inhibition of CDC2 kinase activity by the flavonoid L86-8275. Biochem. Biophys. Res. Commun. 201, 589–595 (1994).
3. Sanchez-Martinez, C., Lallena, M. J., Sanfeliciano, S. G. & de Dios, A. Cyclin dependent kinase (CDK) inhibitors as anticancer drugs: recent advances (2015-2019). Bioorg. Med. Chem. Lett. 29, 126637 (2019).
4. Malumbres, M. Cyclin-dependent kinases. Genome Biol. 15, 122 (2014).
5. Malumbres, M. et al. Mammalian cells cycle without the D-type cyclin-dependent kinases Cdk4 and Cdk6. Cell 118, 493–504 (2004). Using Cdk4 and Cdk6 double-knockout mice, this study establishes that mammalian cells can proliferate in the absence of both CDK4 and CDK6, demonstrating a plasticity of cyclin–CDK networks that has implications for CDK4/6 inhibitor resistance.
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