Combined EGFR and autophagy modulation impairs cell migration and enhances radiosensitivity in human glioblastoma cells
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Updated: May 1, 2026

Generation of CAR T Cells for Adoptive Therapy in the Context of Glioblastoma Standard of Care
Published on: February 16, 2015
Silvia Palumbo1, Paolo Tini, Marzia Toscano
1Department of Biology and Biotechnology, University of Pavia, Pavia, Italy.
Abstract:
Glioblastoma (GBM) remains the most aggressive and lethal brain tumor due to its molecular heterogeneity and high motility and invasion capabilities of its cells, resulting in high resistance to current standard treatments (surgery, followed by ionizing radiation combined with Temozolomide chemotherapy administration). Locus amplification, gene overexpression, and genetic mutations of epidermal growth factor receptor (EGFR) are hallmarks of GBM that can ectopically activate downstream signaling oncogenic cascades such as PI3K/Akt/mTOR pathway. Importantly, alteration of this pathway, involved also in the regulation of autophagy process, can improve radioresistance in GBM cells, thus promoting the aggressive phenotype of this tumor. In this work, the endogenous EGFR expression profile and autophagy were modulated to increase radiosensitivity behavior of human T98G and U373MG GBM cells. Our results primarily indicated that EGFR interfering induced radiosensitivity according to a decrease of the clonogenic capability of the investigated cells, and an effective reduction of the in vitro migratory features. Moreover, EGFR interfering resulted in an increase of Temozolomide (TMZ) cytotoxicity in T98G TMZ-resistant cells. In order to elucidate the involvement of the autophagy process as pro-death or pro-survival role in cells subjected to EGFR interfering, the key autophagic gene ATG7 was silenced, thereby producing a transient block of the autophagy process. This autophagy inhibition rescued clonogenic capability of irradiated and EGFR-silenced T98G cells, suggesting a pro-death autophagy contribution. To further confirm the functional interplay between EGFR and autophagy pathways, Rapamycin-mediated autophagy induction during EGFR modulation promoted further impairment of irradiated cells, in terms of clonogenic and migration capabilities. Taken together, these results might suggest a novel combined EGFR-autophagy modulation strategy, to overcome intrinsic GBM radioresistance, thus improving the efficacy of standard treatments. J. Cell. Physiol. 229: 1863-1873, 2014. © 2014 Wiley Periodicals, Inc.
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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