Ontology highlight
ABSTRACT: Introduction
NRG1 rearrangements produce chimeric ligands that subvert the ERBB pathway to drive tumorigenesis. A better understanding of the signaling networks that mediate transformation by NRG1 fusions is needed to inform effective therapeutic strategies. Unfortunately, this has been hampered by a paucity of patient-derived disease models that faithfully recapitulate this molecularly defined cancer subset.Methods
Patient-derived xenograft (PDX) and cell line models were established from NRG1-rearranged lung adenocarcinoma samples. Transcriptomic, proteomic, and biochemical analyses were performed to identify activated pathways. Efficacy studies were conducted to evaluate HER3- and MTOR-directed therapies.Results
We established a pair of PDX and cell line models o
SUBMITTER: Odintsov I
PROVIDER: S-EPMC9261529 | biostudies-literature | 2021 Jul
REPOSITORIES: biostudies-literature