Faculty, Staff and Student Publications
Publication Date
5-9-2025
Journal
Nature Communications
Abstract
Understanding mechanisms of resistance to active therapies is crucial for developing more effective treatments. Here, we investigate resistance to anti-EGFR and anti-VEGF plus chemotherapy treatment in colorectal cancer (CRC) patients from the IMblaze370 trial (NCT02788279). While anti-VEGF does not select for secondary mutations, anti-EGFR leads to simultaneous mutations in EGFR and MAPK, but not PI3K pathway genes. Notably, we observe frequent acquired mutations in the EGFR extracellular but not intracellular domain and that patients with higher baseline expression of EGFR-ligands are prone to acquire resistant mutations. This data reveals a ligand-activated EGFR/MAPK-signaling dependency in CRC. We also observe enrichment for 8q gains in anti-EGFR treated patients, potentially linked to MYC amplification, a finding further supported by baseline expression analysis. This work adds to the evidence supporting broader evaluation of EGFR and pan-KRAS inhibitor combinations in CRC patients. It also underscores the utility of EGFR ligands as anti-EGFR efficacy biomarkers and provides a rationale for developing ligand blockers to complement and/or improve conventional anti-EGFR therapies in CRC.
Keywords
Female, Humans, Male, Antineoplastic Combined Chemotherapy Protocols, Cetuximab, Colorectal Neoplasms, Drug Resistance, Neoplasm, ErbB Receptors, Ligands, MAP Kinase Signaling System, Mutation, Phosphatidylinositol 3-Kinases, Protein Kinase Inhibitors, Signal Transduction, Vascular Endothelial Growth Factor A
DOI
10.1038/s41467-025-59588-3
PMID
40346041
PMCID
PMC12064836
PubMedCentral® Posted Date
5-9-2025
PubMedCentral® Full Text Version
Post-print
Published Open-Access
yes
Included in
Bioinformatics Commons, Biomedical Informatics Commons, Genetic Phenomena Commons, Medical Genetics Commons, Oncology Commons