EGFRvIII Confers Sensitivity to Saracatinib in a STAT5-Dependent Manner in Glioblastoma

Int J Mol Sci. 2024 Jun 6;25(11):6279. doi: 10.3390/ijms25116279.

Abstract

Glioblastoma (GBM) is the most common primary malignant brain tumor in adults, with few effective treatments. EGFR alterations, including expression of the truncated variant EGFRvIII, are among the most frequent genomic changes in these tumors. EGFRvIII is known to preferentially signal through STAT5 for oncogenic activation in GBM, yet targeting EGFRvIII has yielded limited clinical success to date. In this study, we employed patient-derived xenograft (PDX) models expressing EGFRvIII to determine the key points of therapeutic vulnerability within the EGFRvIII-STAT5 signaling axis in GBM. Our findings reveal that exogenous expression of paralogs STAT5A and STAT5B augments cell proliferation and that inhibition of STAT5 phosphorylation in vivo improves overall survival in combination with temozolomide (TMZ). STAT5 phosphorylation is independent of JAK1 and JAK2 signaling, instead requiring Src family kinase (SFK) activity. Saracatinib, an SFK inhibitor, attenuates phosphorylation of STAT5 and preferentially sensitizes EGFRvIII+ GBM cells to undergo apoptotic cell death relative to wild-type EGFR. Constitutively active STAT5A or STAT5B mitigates saracatinib sensitivity in EGFRvIII+ cells. In vivo, saracatinib treatment decreased survival in mice bearing EGFR WT tumors compared to the control, yet in EGFRvIII+ tumors, treatment with saracatinib in combination with TMZ preferentially improves survival.

Keywords: cell signaling; glioblastoma; precision oncology; receptor tyrosine kinase.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Benzodioxoles* / pharmacology
  • Benzodioxoles* / therapeutic use
  • Brain Neoplasms / drug therapy
  • Brain Neoplasms / genetics
  • Brain Neoplasms / metabolism
  • Brain Neoplasms / pathology
  • Cell Line, Tumor
  • Cell Proliferation* / drug effects
  • ErbB Receptors* / metabolism
  • Glioblastoma* / drug therapy
  • Glioblastoma* / genetics
  • Glioblastoma* / metabolism
  • Glioblastoma* / pathology
  • Humans
  • Mice
  • Phosphorylation / drug effects
  • Quinazolines* / pharmacology
  • Quinazolines* / therapeutic use
  • STAT5 Transcription Factor* / metabolism
  • Signal Transduction / drug effects
  • Temozolomide* / pharmacology
  • Tumor Suppressor Proteins
  • Xenograft Model Antitumor Assays
  • src-Family Kinases / metabolism

Substances

  • STAT5 Transcription Factor
  • Quinazolines
  • epidermal growth factor receptor VIII
  • Benzodioxoles
  • ErbB Receptors
  • saracatinib
  • STAT5A protein, human
  • Temozolomide
  • STAT5B protein, human
  • src-Family Kinases
  • Tumor Suppressor Proteins