| Literature DB >> 35709750 |
Allison Pribnow1, Barbara Jonchere1, Jingjing Liu2, Kyle S Smith3, Olivia Campagne4, Ke Xu5, Sarah Robinson1, Yogesh Patel3, Arzu Onar-Thomas6, Gang Wu5, Clinton F Stewart4, Paul A Northcott3, Jiyang Yu2, Giles W Robinson7, Martine F Roussel1.
Abstract
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. ©2022 The Authors; Published by the American Association for Cancer Research.Entities:
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Year: 2022 PMID: 35709750 PMCID: PMC9578677 DOI: 10.1158/1535-7163.MCT-21-0598
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.009