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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 5:

Figure 5:

Abemaciclib slows tumor growth in IDH-mutant glioma models with CDKN2A deletion. (A) Tumor volumes of TS603 subcutaneous xenografts in animals treated with abemaciclib (N = 6) or vehicle control (N = 7) five times per week. Bars ± SEM. (B) Ratio of phospho-Rb to total Rb detected in each tumor taken at study endpoint show reduction to a mean of 0.8 in abemaciclib treated tumors compared to 1.4 for vehicle treated tumors. Comparison based on unpaired t-test, p = 0.02. (C) Survival curve of mice bearing intracranial xenografts of MGG152-CDKN2A−/− sgRNA3 treated five times per week with abemaciclib (N = 8) or vehicle (N = 8). One animal in Abemaciclib group censored due to unrelated dermatologic issue. (D) Representative images of immunohistochemistry of tumors extracted from vehicle or abemaciclib-treated animals, showing IDH1 R132H, Ki-67 and phosphorylated Rb (p-Rb).