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Imaging NRF2 activation in non-small cell lung cancer with positron emission tomography

  • Hannah E. Greenwood,
  • Abigail R. Barber,
  • Richard S. Edwards,
  • Will E. Tyrrell,
  • Madeleine E. George,
  • Sofia N. dos Santos,
  • Friedrich Baark,
  • Muhammet Tanc,
  • Eman Khalil,
  • Aimee Falzone,
  • Nathan P. Ward,
  • Janine M. DeBlasi,
  • Laura Torrente,
  • Pritin N. Soni,
  • David R. Pearce,
  • George Firth,
  • Lydia M. Smith,
  • Oskar Vilhelmsson Timmermand,
  • Ariana Huebner,
  • Charles Swanton,
  • Robert E. Hynds,
  • Gina M. DeNicola,
  • Timothy H. Witney

摘要

Mutations in the NRF2-KEAP1 pathway are common in non-small cell lung cancer (NSCLC) and confer broad-spectrum therapeutic resistance, leading to poor outcomes. Currently, there is no means to non-invasively identify NRF2 activation in living subjects. Here, we show that positron emission tomography imaging with the system xc radiotracer, [18F]FSPG, provides a sensitive and specific marker of NRF2 activation in orthotopic, patient-derived, and genetically engineered mouse models of NSCLC. We found a NRF2-related gene expression signature in a large cohort of NSCLC patients, suggesting an opportunity to preselect patients prior to [18F]FSPG imaging. Furthermore, we reveal that system xc is a metabolic vulnerability that can be therapeutically targeted with an antibody-drug conjugate for sustained tumour growth suppression. Overall, our results establish [18F]FSPG as a predictive marker of therapy resistance in NSCLC and provide the basis for the clinical evaluation of both imaging and therapeutic agents that target this important antioxidant pathway.