Pan-RAF inhibitor exarafenib targets BRAF class II/III NSCLC and reveals ARAF-KSR1 resistance and combination strategies.

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Title: Pan-RAF inhibitor exarafenib targets BRAF class II/III NSCLC and reveals ARAF-KSR1 resistance and combination strategies.
Authors: Manabe T; Department of Medicine, University of California, San Francisco, San Francisco, CA, USA. tadashi.manabe@ucsf.edu.; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, USA. tadashi.manabe@ucsf.edu.; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA, USA. tadashi.manabe@ucsf.edu., Bergo HC; Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, USA.; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA, USA., Li Q; Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, USA.; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA, USA., Wang TS; Kinnate Biopharma, San Diego, CA, USA., Severson P; Kinnate Biopharma, San Diego, CA, USA., Miller N; Kinnate Biopharma, San Diego, CA, USA., Lee C; Kinnate Biopharma, San Diego, CA, USA., Yay Donderici E; Guardant Health, Redwood City, CA, USA., Zhang N; Guardant Health, Redwood City, CA, USA., Wu W; Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, USA.; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA, USA., Chou YT; Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, USA.; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA, USA., Kerr DL; Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, USA.; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA, USA., Allegakoen P; Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, USA.; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA, USA., Grandinetti KB; Kinnate Biopharma, San Diego, CA, USA., Soroceanu L; Kinnate Biopharma, San Diego, CA, USA., Pelham RJ; Kinnate Biopharma, San Diego, CA, USA., Martin ES; Kinnate Biopharma, San Diego, CA, USA., Murphy EA; Kinnate Biopharma, San Diego, CA, USA., Khanna V; Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA., Neal JW; Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA., Chen CT; Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA., Kato S; Division of Hematology and Oncology, University of California San Diego, Moores Cancer Center, La Jolla, CA, USA., Williams R; Kinnate Biopharma, San Diego, CA, USA., Bivona TG; Department of Medicine, University of California, San Francisco, San Francisco, CA, USA. trever.bivona@ucsf.edu.; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, USA. trever.bivona@ucsf.edu.; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA, USA. trever.bivona@ucsf.edu.; Chan-Zuckerberg Biohub, San Francisco, CA, USA. trever.bivona@ucsf.edu.
Source: Nature communications [Nat Commun] 2026 Feb 07; Vol. 17 (1). Date of Electronic Publication: 2026 Feb 07.
Publication Type: Journal Article
Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2041-1723
DOI:10.1038/s41467-026-69216-3