Combined EGFR and autophagy modulation impairs cell migration and enhances radiosensitivity in human glioblastoma

Silvia Palumbo1, Paolo Tini, Marzia Toscano

  • 1Department of Biology and Biotechnology, University of Pavia, Pavia, Italy.

Insights

Targeting epidermal growth factor receptor (EGFR) and autophagy enhances glioblastoma radiosensitivity. Modulating these pathways increases cell death and reduces migration, offering a novel strategy to improve glioblastoma treatment efficacy.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cell Biology

Background:

  • Glioblastoma (GBM) is a lethal brain tumor with high treatment resistance.
  • EGFR alterations and autophagy dysregulation contribute to GBM's aggressive phenotype and radioresistance.
  • The PI3K/Akt/mTOR pathway links EGFR signaling to autophagy and cell survival.

Purpose of the Study:

  • To investigate the combined effects of modulating epidermal growth factor receptor (EGFR) and autophagy on glioblastoma radiosensitivity.
  • To determine the role of autophagy as a pro-death or pro-survival mechanism in EGFR-modulated GBM cells.
  • To explore a novel therapeutic strategy for overcoming GBM radioresistance.

Main Methods:

  • Silencing of endogenous EGFR expression in T98G and U373MG GBM cells.
  • Modulation of autophagy using ATG7 gene silencing and Rapamycin treatment.
  • Assessment of cell radiosensitivity through clonogenic assays and in vitro migration assays.
  • Evaluation of Temozolomide (TMZ) cytotoxicity in EGFR-silenced and TMZ-resistant GBM cells.

Main Results:

  • EGFR interference significantly reduced GBM cell clonogenic capacity and in vitro migration.
  • EGFR modulation increased Temozolomide (TMZ) cytotoxicity in resistant GBM cells.
  • Autophagy inhibition via ATG7 silencing rescued clonogenic survival, indicating a pro-death role in EGFR-modulated cells.
  • Combined EGFR modulation and autophagy induction further impaired GBM cell survival and migration.

Conclusions:

  • EGFR and autophagy pathways are functionally interconnected in GBM.
  • Targeting both EGFR and autophagy represents a promising strategy to overcome GBM radioresistance.
  • This combined approach may enhance the efficacy of standard glioblastoma treatments like radiation and chemotherapy.

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