| Literature DB >> 34621020 |
Joaquín Arribas1,2, César Serrano3,4, Alfonso García-Valverde5, Jordi Rosell5, Sergi Sayols6, David Gómez-Peregrina5, Daniel F Pilco-Janeta5,7, Iván Olivares-Rivas5, Enrique de Álava8,9, Joan Maurel10, Jordi Rubió-Casadevall11, Anna Esteve12,13, Marta Gut12,13, Claudia Valverde14, Jordi Barretina15, Joan Carles14, George D Demetri16,17, Jonathan A Fletcher7.
Abstract
KIT/PDGFRA oncogenic tyrosine kinase signaling is the central oncogenic event in most gastrointestinal stromal tumors (GIST), which are human malignant mesenchymal neoplasms that often feature myogenic differentiation. Although targeted inhibition of KIT/PDGFRA provides substantial clinical benefit, GIST cells adapt to KIT/PDGFRA driver suppression and eventually develop resistance. The specific molecular events leading to adaptive resistance in GIST remain unclear. By using clinically representative in vitro and in vivo GIST models and GIST patients' samples, we found that the E3 ubiquitin ligase Atrogin-1 (FBXO32)-the main effector of muscular atrophy in cachexia-resulted in the most critical gene derepressed in response to KIT inhibition, regardless the type of KIT primary or secondary mutation. Atrogin-1 in GISTs is transcriptionally controlled by the KIT-FOXO3a axis, thus indicating overlap with Atrogin-1 regulation mechanisms in nonneoplastic muscle cells. Further, Atrogin-1 overexpression was a GIST-cell-specific pro-survival mechanism that enabled the adaptation to KIT-targeted inhibition by apoptosis evasion through cell quiescence. Buttressed on these findings, we established in vitro and in vivo the preclinical proof-of-concept for co-targeting KIT and the ubiquitin pathway to maximize the therapeutic response to first-line imatinib treatment.Entities:
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Year: 2021 PMID: 34621020 DOI: 10.1038/s41388-021-02049-0
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867