cp-31398 and palbociclib

p53-R249S (p53-RS) is frequently detected in human hepatocellular carcinoma (HCC) that is highly associated with hepatitis B infection and aflatoxin B1 exposure. Our previous study showed that CDK4/Cyclin D1 phosphorylates p53-RS at the cancer-derived Ser249 and promotes its interaction with c-Myc in the nucleus, consequently enhancing c-Myc-dependent ribosomal biogenesis and HCC cell proliferation. Here we explored the possibility of co-targeting CDK4 and p53-RS with available small molecule inhibitors as a potential combined therapy for HCC that harbor p53-RS. Indeed, co-treatment of p53-RS-containing, but not wild-type p53 or p53-null, HCC cells with PD-0332991 (PD), a CDK4/6 inhibitor, and CP-31398 (CP), a compound that can restore the intrinsic conformation and transcriptional activity of mutant p53, drastically repressed the c-Myc activation function of p53-RS. This combination of PD with CP exhibited a synergistic effect on the inhibition of HCC cell growth in a p53-RS dependent manner, especially at a lower dose. These results suggest that co-targeting CDK4 and p53-RS can serve as a potential approach for the development of an effective therapy for HCC that harbor p53-RS.

Topics: Apoptosis; Biomarkers, Tumor; Carcinoma, Hepatocellular; Cell Proliferation; Cyclin-Dependent Kinase 4; Drug Synergism; Drug Therapy, Combination; Gene Expression Regulation, Neoplastic; Humans; Liver Neoplasms; Mutation; Phosphorylation; Piperazines; Protein Kinase Inhibitors; Pyridines; Pyrimidines; Tumor Cells, Cultured; Tumor Suppressor Protein p53