CRISPR knockout screens reveal JUN as the master mediator of resistance to MAPK inhibition in KRAS-mutant pancreatic cancer

Alterations in the PI3K/AKT/mTOR and JUN pathways can induce resistance to multiple combinations of MAPK pathway inhibitors, and may serve as biomarkers for sensitivity/resistance in clinical trials exploring such combinations in KRAS-mutant PDAC.

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Publication Details

Journal
Journal of Experimental & Clinical Cancer Research
Published
2026-01-22
DOI
https://doi.org/10.1186/s13046-025-03616-z
Primary Topic
Protein Tyrosine Phosphatases
Type
article
Field-Weighted Citation Impact
0.00
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article

CRISPR knockout screens reveal JUN as the master mediator of resistance to MAPK inhibition in KRAS-mutant pancreatic cancer

Sara Mainardi, R. Bernards, Astrid Bosma, Manon Boeije et al.
Journal of Experimental & Clinical Cancer Research
Protein Tyrosine Phosphatases
article

CRISPR knockout screens reveal JUN as the master mediator of resistance to MAPK inhibition in KRAS-mutant pancreatic cancer

Sara Mainardi, R. Bernards, Astrid Bosma, Manon Boeije, Antonio Mulero‐Sánchez, Cor Lieftink, Niki Pouliopoulou, Bonifiya Visuvasam, Natalie Proost, Roderick Beijersbergen, Marieke van de Ven
article en

Abstract

Alterations in the PI3K/AKT/mTOR and JUN pathways can induce resistance to multiple combinations of MAPK pathway inhibitors, and may serve as biomarkers for sensitivity/resistance in clinical trials exploring such combinations in KRAS-mutant PDAC.

Journal of Experimental & Clinical Cancer ResearchVol. 45(1)
Oncode Institute (NL), Cancer Genomics Centre (NL)
Good health and well-being
Openalex Percentile: Top 80%
Protein Tyrosine Phosphatases
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