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Cell cycle on the crossroad of tumorigenesis and cancer therapy.
Trends Cell Biol. 2022 Jan;32(1):30-44. doi: 10.1016/j.tcb.2021.07.001. Epub 2021 Jul 22.
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PROteolysis TArgeting Chimeras (PROTACs) as emerging anticancer therapeutics.
Oncogene. 2020 Jun;39(26):4909-4924. doi: 10.1038/s41388-020-1336-y. Epub 2020 May 31.
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Proteolysis-targeting chimeras (PROTACs) in cancer therapy.
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Proteolysis targeting chimeras (PROTACs) in cancer therapy.
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Proteolysis-targeting chimeras: A promising technique in cancer therapy for gaining insights into tumor development.
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PROTACs: A novel strategy for cancer therapy.
Semin Cancer Biol. 2020 Dec;67(Pt 2):171-179. doi: 10.1016/j.semcancer.2020.02.006. Epub 2020 Feb 11.
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Proteolysis targeting chimeras (PROTACs) are emerging therapeutics for hematologic malignancies.
J Hematol Oncol. 2020 Jul 27;13(1):103. doi: 10.1186/s13045-020-00924-z.
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MDM2-Based Proteolysis-Targeting Chimeras (PROTACs): An Innovative Drug Strategy for Cancer Treatment.
Int J Mol Sci. 2022 Sep 21;23(19):11068. doi: 10.3390/ijms231911068.
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Peptide-based PROTAC degrader of FOXM1 suppresses cancer and decreases GLUT1 and PD-L1 expression.
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5
A deep single cell mass cytometry approach to capture canonical and noncanonical cell cycle states.
bioRxiv. 2025 Jul 10:2025.07.08.663243. doi: 10.1101/2025.07.08.663243.
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CDK12 inhibition enhances oxaliplatin efficacy in gastric cancer by suppressing the MAPK signaling pathway.
J Gastrointest Oncol. 2025 Jun 30;16(3):823-839. doi: 10.21037/jgo-2025-392. Epub 2025 Jun 23.
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Silencing NEDD4L Effectively Inhibits the Malignant Behaviors of Hepatocellular Carcinoma.
J Hepatocell Carcinoma. 2025 Jul 10;12:1369-1391. doi: 10.2147/JHC.S511466. eCollection 2025.
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PSMD12 promotes hepatocellular carcinoma progression by stabilizing CDK1.
Front Immunol. 2025 Jun 4;16:1581398. doi: 10.3389/fimmu.2025.1581398. eCollection 2025.

本文引用的文献

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TF-PROTACs Enable Targeted Degradation of Transcription Factors.
J Am Chem Soc. 2021 Jun 16;143(23):8902-8910. doi: 10.1021/jacs.1c03852. Epub 2021 Jun 8.
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Cancer Selective Target Degradation by Folate-Caged PROTACs.
J Am Chem Soc. 2021 May 19;143(19):7380-7387. doi: 10.1021/jacs.1c00451. Epub 2021 May 10.
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The AMBRA1 E3 ligase adaptor regulates the stability of cyclin D.
Nature. 2021 Apr;592(7856):794-798. doi: 10.1038/s41586-021-03474-7. Epub 2021 Apr 14.
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CRL4 is a master regulator of D-type cyclins.
Nature. 2021 Apr;592(7856):789-793. doi: 10.1038/s41586-021-03445-y. Epub 2021 Apr 14.
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AMBRA1 regulates cyclin D to guard S-phase entry and genomic integrity.
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Phase II Study of the WEE1 Inhibitor Adavosertib in Recurrent Uterine Serous Carcinoma.
J Clin Oncol. 2021 May 10;39(14):1531-1539. doi: 10.1200/JCO.20.03167. Epub 2021 Mar 11.
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New Insights into CDK Regulators: Novel Opportunities for Cancer Therapy.
Trends Cell Biol. 2021 May;31(5):331-344. doi: 10.1016/j.tcb.2021.01.010. Epub 2021 Mar 3.
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Discovery of a first-in-class CDK2 selective degrader for AML differentiation therapy.
Nat Chem Biol. 2021 May;17(5):567-575. doi: 10.1038/s41589-021-00742-5. Epub 2021 Mar 4.
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Spatiotemporal dissection of the cell cycle with single-cell proteogenomics.
Nature. 2021 Feb;590(7847):649-654. doi: 10.1038/s41586-021-03232-9. Epub 2021 Feb 24.
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Mechanisms of CDK4/6 Inhibitor Resistance in Luminal Breast Cancer.
Front Pharmacol. 2020 Nov 16;11:580251. doi: 10.3389/fphar.2020.580251. eCollection 2020.

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