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The Therapeutic Potential of CDK4/6 Inhibitors, Novel Cancer Drugs, in Kidney Diseases

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2023 Sep 9
PMID 37686364
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Abstract

Inflammation is a crucial pathological feature in cancers and kidney diseases, playing a significant role in disease progression. Cyclin-dependent kinases CDK4 and CDK6 not only contribute to cell cycle progression but also participate in cell metabolism, immunogenicity and anti-tumor immune responses. Recently, CDK4/6 inhibitors have gained approval for investigational treatment of breast cancer and various other tumors. Kidney diseases and cancers commonly exhibit characteristic pathological features, such as the involvement of inflammatory cells and persistent chronic inflammation. Remarkably, CDK4/6 inhibitors have demonstrated impressive efficacy in treating non-cancerous conditions, including certain kidney diseases. Current studies have identified the renoprotective effect of CDK4/6 inhibitors, presenting a novel idea and potential direction for treating kidney diseases in the future. In this review, we briefly reviewed the cell cycle in mammals and the role of CDK4/6 in regulating it. We then provided an introduction to CDK4/6 inhibitors and their use in cancer treatment. Additionally, we emphasized the importance of these inhibitors in the treatment of kidney diseases. Collectively, growing evidence demonstrates that targeting CDK4 and CDK6 through CDK4/6 inhibitors might have therapeutic benefits in various cancers and kidney diseases and should be further explored in the future.

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References
1.
Peyressatre M, Prevel C, Pellerano M, Morris M . Targeting cyclin-dependent kinases in human cancers: from small molecules to Peptide inhibitors. Cancers (Basel). 2015; 7(1):179-237. PMC: 4381256. DOI: 10.3390/cancers7010179. View

2.
Condorelli R, Spring L, OShaughnessy J, Lacroix L, Bailleux C, Scott V . Polyclonal RB1 mutations and acquired resistance to CDK 4/6 inhibitors in patients with metastatic breast cancer. Ann Oncol. 2017; 29(3):640-645. DOI: 10.1093/annonc/mdx784. View

3.
Gupta S, Caza T, Herrmann S, Sakhiya V, Jhaveri K . Clinicopathologic Features of Acute Kidney Injury Associated With CDK4/6 Inhibitors. Kidney Int Rep. 2022; 7(3):618-623. PMC: 8897293. DOI: 10.1016/j.ekir.2021.11.033. View

4.
Liu B, Tang T, Lv L, Lan H . Renal tubule injury: a driving force toward chronic kidney disease. Kidney Int. 2018; 93(3):568-579. DOI: 10.1016/j.kint.2017.09.033. View

5.
Martinez-Alonso D, Malumbres M . Mammalian cell cycle cyclins. Semin Cell Dev Biol. 2020; 107:28-35. DOI: 10.1016/j.semcdb.2020.03.009. View