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April 5, 2026Cancer Research0 citations

Abstract 4868: Modelling glioblastoma sensitivity to irradiation with a patient derived xenograft-derived 3D platform

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FCFu-Ju ChouARAnnamaria RapisardaMZMarianna Zipeto

Key Points

  • The aim is to evaluate glioblastoma sensitivity to irradiation using patient-derived xenograft organoids across different models.
  • Conducted short and long-term viability assays with glioblastoma patient-derived xenografts (PDXOs).
  • Utilized X-ray irradiation at different doses (2 Gy and 4 Gy) in viability assays over 4 and 14 days.
  • Performed morphological assessments and quantified cell viability with the CellTiter-Glo® assay.
  • Monitored organoid integrity and size, focusing on structures ≥50 µm.
  • The 4-day assay revealed generally low sensitivity to irradiation in all models tested.
  • The 14-day assay distinguished between sensitive and resistant models, with up to 92% viability loss in sensitive organoids.
  • Analysis showed that intrinsic tumor biology influenced irradiation responses rather than patient demographic factors.
  • Models with EGFR amplification showed increased susceptibility to irradiation, while resistant models had enriched pathways related to metabolism and oxidative stress.

Abstract

Abstract Glioblastoma (GBM) remains one of the most aggressive and treatment-refractory brain tumors, characterized by profound cellular heterogeneity, infiltrative growth, and intrinsic resistance to conventional therapies, including radiotherapy. To better understand differential tumor responses to irradiation, a series of short Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4868.

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Cite This Study

Chou et al. (2026) studied this question.

synapsesocial.com/papers/69d1fc70a79560c99a0a205fhttps://doi.org/10.1158/1538-7445.am2026-4868
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