DIPG-10. OPTIMAL HDAC INHIBITION IN DIFFUSE INTRINSIC PONTINE GLIOMA. (4th December 2020)

• Record Type: Journal Article
• Authors: Vitanza, Nicholas; Biery, Matt; Myers, Carrie; Ferguson, Eric; Park, Giulia; Noll, Alyssa; Pakiam, Fiona; Girard, Emily; Morris, Shelli; Cole, Bonnie; Brusniak, Mi-Youn; Mhyre, Andrew; Olson, James
• Is Part Of: Neuro-oncology. Volume 22(2020)Supplement 3
• Page Start: iii288
• Page End: iii289
• Publication Date: 2020-12-04
• Subjects: Brain Neoplasms -- Periodicals; Brain -- Tumors -- Periodicals; Brain -- Cancer -- Periodicals; Nervous system -- Cancer -- Periodicals; 616.99481
• DOI: 10.1093/neuonc/noaa222.060
• Languages: English
• ISSNs: 1522-8517

Abstract

Abstract: As the majority of diffuse intrinsic pontine glioma (DIPG) have H3K27M mutations, epigenetic-targeting agents have been studied, though evaluations have been limited by their model systems, untranslatable drug concentrations, and/or evasive mechanisms of action. To develop a more translational model, we used biopsy samples from newly diagnosed DIPG patients to create treatment-naïve in vitro and in vivo models (molecular aberrations in parentheses), including PBT-09FH ( H3FA3, PI3KCA ), PBT-22FH ( H3F3A, TP53 ), PBT-24FH ( PMS2 ), and PBT-27FH ( HIST1H3B, TP53, NTRK2 ). Models demonstrated radiation-resistance similar to the patient from whom the culture was generated, supporting the models' relevance (e.g. cell viability after 8 Gy was 36%, 81%, 71%, and 61% in PBT-09FH, -22FH, -24FH, and -27FH, respectively, compared to 7% in the medulloblastoma model MED-411FH). We evaluated cell viability and apoptosis following treatment with a panel of HDAC inhibitors, identifying the low nanomolar IC50 of quisinostat (~50 nM) and romidepsin (~5 nM). While RNA expression changes induced by 100 nM panobinostat and quisinostat included shared overexpression of the top 20/25 genes (e.g. FSTL5, ITIH5 ) and shared downregulation of the top 22/25 (e.g. GPR37L1, HEPACAM ), only 9/25 were downregulated by panobinostat, quisinostat, and romidepsin (e.g. C21orf62, IFIT2 ), identifying these as potential vulnerabilities or biomarkers of lethal HDAC inhibition. Mass-spectrometry (LC-MS) demonstrated panobinostat as the greatest acetylator of cortactin, potentially related to thrombocytopenia. While PBT-09 flank models demonstrated quisinostat's on-target acetylation and efficacy, orthotopic xenograft models did not, supporting our model's intact blood-brain barrier and emphasizing the need for CNS penetrant versions of potentially efficacious agents.