Elevated FSP1 protects KRAS-mutated cells from ferroptosis during tumor initiation
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Updated: Aug 19, 2025

Author Spotlight: Tracing the Ferroptotic Signatures and Cell Death Dynamics in Medulloblastoma for Advanced Therapeutics
Published on: March 15, 2024
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.
Abstract:
Oncogenic KRAS is the key driver oncogene for several of the most aggressive human cancers. One key feature of oncogenic KRAS expression is an early increase in cellular reactive oxygen species (ROS) which promotes cellular transformation if cells manage to escape cell death, mechanisms of which remain incompletely understood. Here, we identify that expression of oncogenic as compared to WT KRAS in isogenic cellular systems renders cells more resistant to ferroptosis, a recently described type of regulated necrosis. Mechanistically, we find that cells with mutant KRAS show a specific lack of ferroptosis-induced lipid peroxidation. Interestingly, KRAS-mutant cells upregulate expression of ferroptosis suppressor protein 1 (FSP1). Indeed, elevated levels of FSP1 in KRAS-mutant cells are responsible for mediating ferroptosis resistance and FSP1 is upregulated as a consequence of MAPK and NRF2 pathway activation downstream of KRAS. Strikingly, FSP1 activity promotes cellular transformation in soft agar and its overexpression is sufficient to promote spheroid growth in 3D in KRAS WT cells. Moreover, FSP1 expression and its activity in ferroptosis inhibition accelerates tumor onset of KRAS WT cells in the absence of oncogenic KRAS in vivo. Consequently, we find that pharmacological induction of ferroptosis in pancreatic organoids derived from the LsL-KRASG12D expressing mouse model is only effective in combination with FSP1 inhibition. Lastly, FSP1 is upregulated in non-small cell lung cancer (NSCLC), colorectal cancer (CRC) and pancreatic ductal adenocarcinoma (PDAC) as compared to the respective normal tissue of origin and correlates with NRF2 expression in PDAC patient datasets. Based on these data, we propose that KRAS-mutant cells must navigate a ferroptosis checkpoint by upregulating FSP1 during tumor establishment. Consequently, ferroptosis-inducing therapy should be combined with FSP1 inhibitors for efficient therapy of KRAS-mutant cancers.
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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