Widening the Spectrum of Fusion Events in Schwannoma: Identification of a Novel <scp>TANC1</scp>::<scp>HTRA1</scp> Fusion
A range of genomic drivers have been identified in schwannomas, including a number of translocations, most commonly SH3PXD2A::HTRA1. To date, despite the analysis of large numbers of cases, no examples of variant HTRA1 partners have been described. We describe a schwannoma arising in the periportal region in which a novel TANC1::HTRA1 fusion was identified. The identification of this variant expands the range of fusion drivers in schwannoma and offers insight into the pathogenic mechanism of HTRA1 fusions and their utility in molecular diagnosis.
Authors
- Patrick S. Tarpey (ORCID: https://orcid.org/0000-0002-2042-4543)
- James Watkins (ORCID: https://orcid.org/0000-0002-2253-6653)
- John A. Tadross (ORCID: https://orcid.org/0000-0002-8424-1252)
- N. Mohammed (ORCID: https://orcid.org/0009-0009-5167-7517)
- Maria O’Donovan
Institutions
- Cambridge University Hospitals NHS Foundation Trust (GB)
- Wellcome/MRC Institute of Metabolic Science (GB)
Publication Details
- Journal
- Genes Chromosomes and Cancer
- Published
- 2025-08-01
- DOI
- https://doi.org/10.1002/gcc.70072
- Citations
- 1
- Primary Topic
- Neurofibromatosis and Schwannoma Cases
- Type
- article
- Field-Weighted Citation Impact
- 1.39