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UC2288 is an inhibitor of cyclin-dependent kinase inhibitor (p21WAF1), a negative regulator of cell cycle progression.1 It reduces the protein levels and mRNA expression of p21WAF1 independently of Raf and p53, respectively, when used at a concentration of 10 µM. UC2288 (8 µM) decreases the proliferation of, and phosphorylation of EGFR and extracellular-signal-related kinases 1/2 (ERK1/2) in, CNE-2 and 5-8F nasopharyngeal cell lines.2 In vivo, UC2288, in combination with the telomerase inhibitor imetelstat, reduces tumor growth and induces apoptosis in an HCT116 colorectal cancer mouse xenograft model when administered at a dose of 15 mg/kg three times per week.3
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1. A novel p21 attenuator which is structurally related to sorafenib. Cancer Biol. Ther. 14(3), 278-285 (2013).
2. UC2288 induces cell apoptosis of nasopharyngeal carcinoma cells via inhibiting EGFR/ERK pathway. J. Cancer 12(4), 988-995 (2021).
3. Synergistic tumor suppression by combined inhibition of telomerase and CDKN1A. Proc. Natl. Acad. Sci. USA 111(30), E3062-E3071 (2014).