| Literature DB >> 32358191 |
Kruttika Bhat1, Mohammad Saki1, Erina Vlashi1,2, Fei Cheng1, Sara Duhachek-Muggy1, Claudia Alli1, Garrett Yu1, Paul Medina1, Ling He1, Robert Damoiseaux2,3, Matteo Pellegrini4, Nathan R Zemke5, Phioanh Leia Nghiemphu2,6, Timothy F Cloughesy2,6, Linda M Liau2,7, Harley I Kornblum2,8, Frank Pajonk9,2.
Abstract
Glioblastoma (GBM) is the deadliest adult brain cancer, and all patients ultimately succumb to the disease. Radiation therapy (RT) provides survival benefit of 6 mo over surgery alone, but these results have not improved in decades. We report that radiation induces a glioma-initiating cell phenotype, and we have identified trifluoperazine (TFP) as a compound that interferes with this phenotype conversion. TFP causes loss of radiation-induced Nanog mRNA expression, and activation of GSK3 with consecutive posttranslational reduction in p-Akt, Sox2, and β-catenin protein levels. TFP did not alter the intrinsic radiation sensitivity of glioma-initiating cells (GICs). Continuous treatment with TFP and a single dose of radiation reduced the number of GICs in vivo and prolonged survival in syngeneic and patient-derived orthotopic xenograft (PDOX) mouse models of GBM. Our findings suggest that the combination of a dopamine receptor antagonist with radiation enhances the efficacy of RT in GBM by preventing radiation-induced phenotype conversion of radiosensitive non-GICs into treatment-resistant, induced GICs (iGICs).Entities:
Keywords: dedifferentiation; dopamine receptor antagonist; glioblastoma; glioma-initiating cells; radiation
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Year: 2020 PMID: 32358191 PMCID: PMC7245100 DOI: 10.1073/pnas.1920154117
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205