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. Author manuscript; available in PMC: 2025 Jan 15.
Published in final edited form as: Clin Cancer Res. 2024 Jul 15;30(14):2996–3005. doi: 10.1158/1078-0432.CCR-24-0562

Figure 2:

Figure 2:

Loss of p16 enhances sensitivity of IDH-mutant glioma lines to CDK4/6 inhibition. A. Western blot of parental and CDKN2A knockout MGG152 lines showing loss of p16 expression and changes in Rb phosphorylation in the presence of abemaciclib treatment (300 nM). Cyclophilin B is used as a loading control. B. Cell viability assay of MGG152 lines after exposure to abemaciclib at the indicated concentrations for 5 days. C. Cell viability following abemaciclib treatment at 100 nM. n = 3 for each concentration, bars ± SEM. Data are representative of three biological replicates. **** p < 0.0001.