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Adeno-to-squamous transition drives resistance to KRAS inhibition in LKB1 mutant lung cancer.

Authors :
Tong X
Patel AS
Kim E
Li H
Chen Y
Li S
Liu S
Dilly J
Kapner KS
Zhang N
Xue Y
Hover L
Mukhopadhyay S
Sherman F
Myndzar K
Sahu P
Gao Y
Li F
Li F
Fang Z
Jin Y
Gao J
Shi M
Sinha S
Chen L
Chen Y
Kheoh T
Yang W
Yanai I
Moreira AL
Velcheti V
Neel BG
Hu L
Christensen JG
Olson P
Gao D
Zhang MQ
Aguirre AJ
Wong KK
Ji H
Source :
Cancer cell [Cancer Cell] 2024 Mar 11; Vol. 42 (3), pp. 413-428.e7. Date of Electronic Publication: 2024 Feb 22.
Publication Year :
2024

Abstract

KRAS <superscript>G12C</superscript> inhibitors (adagrasib and sotorasib) have shown clinical promise in targeting KRAS <superscript>G12C</superscript> -mutated lung cancers; however, most patients eventually develop resistance. In lung patients with adenocarcinoma with KRAS <superscript>G12C</superscript> and STK11/LKB1 co-mutations, we find an enrichment of the squamous cell carcinoma gene signature in pre-treatment biopsies correlates with a poor response to adagrasib. Studies of Lkb1-deficient KRAS <superscript>G12C</superscript> and Kras <superscript>G12D</superscript> lung cancer mouse models and organoids treated with KRAS inhibitors reveal tumors invoke a lineage plasticity program, adeno-to-squamous transition (AST), that enables resistance to KRAS inhibition. Transcriptomic and epigenomic analyses reveal ΔNp63 drives AST and modulates response to KRAS inhibition. We identify an intermediate high-plastic cell state marked by expression of an AST plasticity signature and Krt6a. Notably, expression of the AST plasticity signature and KRT6A at baseline correlates with poor adagrasib responses. These data indicate the role of AST in KRAS inhibitor resistance and provide predictive biomarkers for KRAS-targeted therapies in lung cancer.<br />Competing Interests: Declaration of interests A.J.A. has consulted for Anji Pharmaceuticals, Arrakis Therapeutics, AstraZeneca, Boehringer Ingelheim, Oncorus, Inc., Merck & Co., Inc., Mirati Therapeutics, Nimbus Therapeutics, Plexium, Revolution Medicines, Reactive Biosciences, Riva Therapeutics, Servier Pharmaceuticals, Syros Pharmaceuticals, T-knife Therapeutics. A.J.A. holds equity in Riva Therapeutics. A.J.A. has received research funding from Bristol Myers Squibb, Deerfield, Inc., Eli Lilly, Mirati Therapeutics, Novartis, Novo Ventures, Revolution Medicines, and Syros Pharmaceuticals. K.-K.W. has research funding and/or consulted for Janssen Pharmaceuticals, Pfizer, Bristol Myers Squibb, Zentalis Pharmaceuticals, Blueprint Medicines, Takeda Pharmaceuticals, Mirati Therapeutics, Novartis, Genentech, Merus, Bridgebio Pharma, Xilio Therapeutics, Allerion Therapeutics, Boehringer Ingelheim, Cogent Therapeutics, Revolution Medicines and AstraZeneca.<br /> (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1878-3686
Volume :
42
Issue :
3
Database :
MEDLINE
Journal :
Cancer cell
Publication Type :
Academic Journal
Accession number :
38402609
Full Text :
https://doi.org/10.1016/j.ccell.2024.01.012