ERK signaling promotes resistance to TRK kinase inhibition in NTRK fusion-driven glioma mouse models.
Sebastian SchmidZachary R RussellAlex Shimura YamashitaMadeline E WestAbigail G ParrishJulia WalkerDmytro RudoyJames Z YanDavid C QuistBetemariyam N GessesseNeriah AlvinezPatrick J CiminoDebra K KumasakaRalph E ParchmentEric C HollandFrank SzulzewskyPublished in: bioRxiv : the preprint server for biology (2024)
Pediatric-type high-grade gliomas frequently harbor gene fusions involving receptor tyrosine kinase genes, including neurotrophic tyrosine kinase receptor (NTRK) fusions. Clinically, these tumors show high initial response rates to tyrosine kinase inhibition but ultimately recur due to the accumulation of additional resistance-conferring mutations. Here, we developed a series of genetically engineered mouse models of treatment-naïve and -experienced NTRK1/2/3 fusion-driven gliomas. Both the TRK kinase domain and the N-terminal fusion partners influenced tumor histology and aggressiveness. Treatment with TRK kinase inhibitors significantly extended survival of NTRK fusion-driven glioma mice in a fusion- and inhibitor-dependent manner, but tumors ultimately recurred due to the presence of treatment-resistant persister cells. Finally, we show that ERK activation promotes resistance to TRK kinase inhibition and identify MEK inhibition as a potential combination therapy. These models will be invaluable tools for preclinical testing of novel inhibitors and to study the cellular responses of NTRK fusion-driven gliomas to therapy.
Keyphrases
- tyrosine kinase
- high grade
- epidermal growth factor receptor
- combination therapy
- mouse model
- signaling pathway
- cell proliferation
- pi k akt
- stem cells
- genome wide
- type diabetes
- induced apoptosis
- cell cycle arrest
- gene expression
- adipose tissue
- oxidative stress
- hepatitis c virus
- copy number
- climate change
- binding protein
- transcription factor
- replacement therapy
- antiretroviral therapy
- hiv infected
- human health