Vertical RAS-pathway inhibition in pancreatic cancer drives therapeutically exploitable mitochondrial alterations

Hafner, P.; Keller, S.; Chen, X.; Alrawashdeh, A.; Jumaa, H.; Nollmann, F.; Besson, S.; Kemming, J.; Gorka, O.; Das, T.; Appiah, B.; Lehmann, A.; Li, M.; Apostolova, P.; Bengsch, B.; Tholen, S.; Schilling, O.; Gross, O.; Vlachos, A.; Wittel, U.; von Elverfeldt, D.; Reichardt, W.; Boerries, M.; Andrieux, G.; Heynen, G.; Fichtner-Feigl, S.; Hannibal, L.; Ruess, D.

doi:10.1101/2025.02.03.636222

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bioRxiv · 10.1101/2025.02.03.636222

Vertical RAS-pathway inhibition in pancreatic cancer drives therapeutically exploitable mitochondrial alterations

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Abstract

Background & AimsOncogenic KRAS mutations drive metabolic rewiring in pancreatic ductal adenocarcinoma (PDAC). Src-homology 2 domain-containing phosphatase 2 (SHP2) is essential for full KRAS activity and promising dual SHP2/mitogen-activated protein kinase (MAPK) inhibition is currently being tested in clinical trials. Exploitable metabolic adaptations may contribute to an invariably evolving resistance. MethodsTo understand the metabolic changes induced by dual inhibition, we comprehensively tested cell lines, endogenous tumor models, and patient-derived organoids representing the full spectrum of PDAC molecular subtypes. ResultsWe find that dual SHP2/mitogen-activated protein kinase kinase (MEK1/2) inhibition induces major mitochondrial alterations, elevates reactive oxygen species (ROS) levels and triggers a lipid peroxidase dependency. While anabolic pathways, glycolysis and autophagy were also affected, mitochondrial alterations persisted longterm into a therapy resistant state. ConclusionsThe resulting vulnerability to induction of ferroptotic cell death via combined SHP2/MEK1/2 and glutathione peroxidase (GPX4) inhibition provides a metabolic lever to reinforce RAS-pathway inhibition for targeted PDAC treatment.

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Hafner, P., Keller, S., Chen, X., Alrawashdeh, A., Jumaa, H., Nollmann, F., Besson, S., Kemming, J., Gorka, O., Das, T., Appiah, B., Lehmann, A., Li, M., Apostolova, P., Bengsch, B., Tholen, S., Schilling, O., Gross, O., Vlachos, A., Wittel, U., von Elverfeldt, D., Reichardt, W., Boerries, M., Andrieux, G., Heynen, G., Fichtner-Feigl, S., Hannibal, L., Ruess, D.. 2025-02-08. Vertical RAS-pathway inhibition in pancreatic cancer drives therapeutically exploitable mitochondrial alterations. https://doi.org/10.1101/2025.02.03.636222

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