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.

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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
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article

Widening the Spectrum of Fusion Events in Schwannoma: Identification of a Novel TANC1::HTRA1 Fusion

Patrick S. Tarpey, James Watkins, John A. Tadross, N. Mohammed et al.
1 citations
Genes Chromosomes and Cancer
Neurofibromatosis and Schwannoma Cases
1.39
article

Widening the Spectrum of Fusion Events in Schwannoma: Identification of a Novel TANC1::HTRA1 Fusion

Patrick S. Tarpey, James Watkins, John A. Tadross, N. Mohammed, Maria O’Donovan
article en
1 citations

Abstract

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.

Genes Chromosomes and CancerVol. 64(8)
Cambridge University Hospitals NHS Foundation Trust (GB), Wellcome/MRC Institute of Metabolic Science (GB)
Openalex Percentile: Top 17%
Neurofibromatosis and Schwannoma Cases
1.39
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