NTRK3 kinase fusions in Spitz tumours
Citations Over TimeTop 10% of 2016 papers
Abstract
Oncogenic fusions in TRK family receptor tyrosine kinases have been identified in several cancers and can serve as therapeutic targets. We identified ETV6-NTRK3, MYO5A-NTRK3 and MYH9-NTRK3 fusions in Spitz tumours, and demonstrated that NTRK3 fusions constitutively activate the mitogen-activated protein kinase, phosphoinositide 3-kinase and phospholipase Cγ1 pathways in melanocytes. This signalling was inhibited by DS-6051a, a small-molecule inhibitor of NTRK1/2/3 and ROS1. NTRK3 fusions expand the range of oncogenic kinase fusions in melanocytic neoplasms and offer targets for a small subset of melanomas for which no targeted options currently exist. Copyright © 2016 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
Related Papers
- → Tyrosine phosphorylation and tyrosine kinase activity of the trk proto-oncogene product induced by NGF(1991)1,058 cited
- → Neurotrophin receptor tyrosine kinases regulated with near-infrared light(2019)75 cited
- → Cellular Assays for High-Throughput Screening for Modulators of Trk Receptor Tyrosine Kinases(2008)17 cited
- → Characterisation of five novel zebrafish Eph-related receptor tyrosine kinases suggests roles in patterning the neural plate(1997)37 cited
- → Rapid Clinical and Radiologic Responses With Larotrectinib Treatment in a Patient With TRK-Fusion–Positive Metastatic Lung Cancer(2019)4 cited