Elevated FSP1 protects KRAS-mutated cells from ferroptosis during tumor initiation

Fabienne Müller1,2, Jonathan K M Lim3, Christina M Bebber1,2

  • 1University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Translational Genomics, Cologne, Germany.

Insights

Oncogenic KRAS mutations promote cancer cell resistance to ferroptosis by upregulating ferroptosis suppressor protein 1 (FSP1). Inhibiting FSP1 alongside ferroptosis-inducing therapies may improve outcomes for KRAS-mutant cancers.

Area of Science:

  • Oncology
  • Cell Death Mechanisms
  • Cancer Biology

Background:

  • Oncogenic KRAS drives aggressive cancers and increases reactive oxygen species (ROS).
  • KRAS-mutant cells exhibit resistance to cell death, but mechanisms are unclear.
  • Ferroptosis is a regulated necrosis pathway crucial in cancer progression.

Purpose of the Study:

  • To investigate the role of KRAS in ferroptosis resistance.
  • To identify mechanisms by which KRAS mutations confer ferroptosis resistance.
  • To evaluate FSP1 as a therapeutic target in KRAS-mutant cancers.

Main Methods:

  • Isogenic cell systems comparing WT KRAS and oncogenic KRAS.
  • Analysis of ferroptosis markers, including lipid peroxidation.
  • Assessment of ferroptosis suppressor protein 1 (FSP1) expression and activity.
  • In vivo tumor models and organoid studies.
  • Analysis of patient datasets for NSCLC, CRC, and PDAC.

Main Results:

  • Oncogenic KRAS confers resistance to ferroptosis by reducing lipid peroxidation.
  • KRAS-mutant cells upregulate FSP1 via MAPK and NRF2 pathways.
  • FSP1 overexpression promotes cellular transformation and tumor growth.
  • FSP1 inhibition is necessary for ferroptosis-inducing therapy efficacy in KRAS-mutant models.
  • FSP1 is upregulated in NSCLC, CRC, and PDAC, correlating with NRF2 in PDAC.

Conclusions:

  • KRAS-mutant cells overcome ferroptosis through FSP1 upregulation, acting as a ferroptosis checkpoint.
  • Targeting FSP1 in combination with ferroptosis inducers offers a potential therapeutic strategy for KRAS-driven cancers.

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