Combination of Ribociclib and Gemcitabine for the Treatment of Medulloblastoma.
Allison PribnowBarbara JonchereJingJing LiuKyle S SmithOlivia CampagneKe XuSarah RobinsonYogesh PatelArzu Onar-ThomasGang WuClinton F StewartPaul A NorthcottJiyang YuGiles W RobinsonMartine F RousselPublished in: Molecular cancer therapeutics (2022)
Group3 (G3) medulloblastoma (MB) is one of the deadliest forms of the disease for which novel treatment is desperately needed. Here we evaluate ribociclib, a highly selective CDK4/6 inhibitor, with gemcitabine in mouse and human G3MBs. Ribociclib central nervous system (CNS) penetration was assessed by in vivo microdialysis and by IHC and gene expression studies and found to be CNS-penetrant. Tumors from mice treated with short term oral ribociclib displayed inhibited RB phosphorylation, downregulated E2F target genes, and decreased proliferation. Survival studies to determine the efficacy of ribociclib and gemcitabine combination were performed on mice intracranially implanted with luciferase-labeled mouse and human G3MBs. Treatment of mice with the combination of ribociclib and gemcitabine was well tolerated, slowed tumor progression and metastatic spread, and increased survival. Expression-based gene activity and cell state analysis investigated the effects of the combination after short- and long-term treatments. Molecular analysis of treated versus untreated tumors showed a significant decrease in the activity and expression of genes involved in cell-cycle progression and DNA damage response, and an increase in the activity and expression of genes implicated in neuronal identity and neuronal differentiation. Our findings in both mouse and human patient-derived orthotopic xenograft models suggest that ribociclib and gemcitabine combination therapy warrants further investigation as a treatment strategy for children with G3MB.
Keyphrases
- combination therapy
- cell cycle
- poor prognosis
- gene expression
- endothelial cells
- dna damage response
- genome wide
- squamous cell carcinoma
- cell proliferation
- computed tomography
- stem cells
- young adults
- induced pluripotent stem cells
- mesenchymal stem cells
- high fat diet induced
- single cell
- binding protein
- adipose tissue
- oxidative stress
- high resolution
- skeletal muscle
- long non coding rna
- mass spectrometry
- replacement therapy
- case control