A novel TRKB-activating internal tandem duplication characterizes a new mechanism of receptor tyrosine kinase activation

Precision medicine programs like the Zero Childhood Cancer Program perform comprehensive molecular analysis of patient tumors, enabling detection of novel structural variants that may be cryptic to standard techniques. Identification of these variants can impact individual patient treatment, and beyond this establish new mechanisms of oncogenic activation. We have identified a novel internal tandem duplication (ITD) in the receptor tyrosine kinase (RTK), NTRK2, in a patient with FOXR2-activated CNS neuroblastoma. The ITD spans exons 10-13 of NTRK2 encoding the transmembrane domain. NTRK2 ITD is transforming and sensitive to TRK inhibition. In silico structural predictions suggested the duplication of an alpha-helix region and juxtaposed tyrosine residues that play a role in facilitating autophosphorylation. Consistent with this, mutation of these residues inhibited cellular transformation. This is the first report of an ITD spanning the transmembrane domain of an RTK, characterizing an additional mechanism by which RTKs are activated in cancer.

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Publication Details

Journal
npj Precision Oncology
Published
2025-05-10
DOI
https://doi.org/10.1038/s41698-025-00928-3
Citations
1
Primary Topic
Neuroblastoma Research and Treatments
Type
article
Field-Weighted Citation Impact
1.39

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article

A novel TRKB-activating internal tandem duplication characterizes a new mechanism of receptor tyrosine kinase activation

Pamela Ajuyah, Fatimah Jalud, Gábor Tax, Paulette Barahona et al.
1 citations
npj Precision Oncology
Neuroblastoma Research and Treatments
1.39
article

A novel TRKB-activating internal tandem duplication characterizes a new mechanism of receptor tyrosine kinase activation

Pamela Ajuyah, Fatimah Jalud, Gábor Tax, Paulette Barahona, M. Emmy M. Dolman, Pablo Acera Mateos, Marie Wong, Lauren M. Brown, Teresa Sadras, Chelsea Mayoh, Loretta M. S. Lau, Mark J. Cowley, Jie Mao, Paul G. Ekert, Antoine de Weck, Steve Foresto, Thomas Robertson
article en
1 citations

Abstract

Precision medicine programs like the Zero Childhood Cancer Program perform comprehensive molecular analysis of patient tumors, enabling detection of novel structural variants that may be cryptic to standard techniques. Identification of these variants can impact individual patient treatment, and beyond this establish new mechanisms of oncogenic activation. We have identified a novel internal tandem duplication (ITD) in the receptor tyrosine kinase (RTK), NTRK2, in a patient with FOXR2-activated CNS neuroblastoma. The ITD spans exons 10-13 of NTRK2 encoding the transmembrane domain. NTRK2 ITD is transforming and sensitive to TRK inhibition. In silico structural predictions suggested the duplication of an alpha-helix region and juxtaposed tyrosine residues that play a role in facilitating autophosphorylation. Consistent with this, mutation of these residues inhibited cellular transformation. This is the first report of an ITD spanning the transmembrane domain of an RTK, characterizing an additional mechanism by which RTKs are activated in cancer.

npj Precision OncologyVol. 9(1)
The University of Melbourne (AU), Peter MacCallum Cancer Centre (AU), Cancer Institute of New South Wales (AU), UNSW Sydney (AU), Sydney Children's Hospital (AU), Children's Health Queensland Hospital and Health Service (AU)
National Health and Medical Research Council
Good health and well-being
Openalex Percentile: Top 20%
Neuroblastoma Research and Treatments
1.39
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