In-frame insertions of SOX10 are highly enriched and characterize a distinct transcriptomic profile in gastrointestinal schwannomas

Pei Hang Lee, Shih Chiang Huang, Jen Chieh Lee, Sung Chou Li, Jen Wei Tsai, Yi Ming Chang, Yu Chien Kao, Wen Lang Fan, Ching Di Chang, Hui Chun Chen, Chih Hao Li, Chia Fa Hu, Ting Ting Liu, Pao Shu Wu, Mann Hua Nam, Shih Chen Yu, Jui Chu Wang, Hsuan Ying Huang

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Gastrointestinal schwannomas are molecularly and histologically distinct from their non-gastrointestinal counterparts, lacking NF2 alterations, although the primary drivers of these tumors are barely understood. A recent study has identified SOX10 in-frame insertions in schwannomas, particularly in intracranial non-vestibular lesions, whereas their role in gastrointestinal schwannomas remains unexplored. Whole exome sequencing of 15 gastrointestinal and two non-gastrointestinal schwannomas revealed recurrent SOX10 in-frame insertions in 14 gastrointestinal cases (93%) without other nerve sheath tumor-related alterations, such as NF2 mutations or SH3PXD2A::HTRA1 fusions (~14% in non-gastrointestinal cases). The prevalence, mutation spectrum, and specificity of SOX10 insertions were validated using Sanger sequencing in a large cohort comprising 61 gastrointestinal and 98 non-gastrointestinal schwannomas, as well as 110 non-schwannomatous mesenchymal and melanocytic neoplasms. SOX10 insertions, occurring within or near the high mobility group box domain, were significantly enriched in gastrointestinal schwannomas (91.8%) compared with non-gastrointestinal cases (5.1%). The most common insertion, p.Y173_Q174insKY, was present in 86.9% of gastrointestinal schwannomas but absent in non-gastrointestinal cases. Another recurrent insertion, p.P175_R176insKYQP, was rare and exclusively found in non-gastrointestinal schwannomas (3/98), while all non-schwannomatous controls were SOX10-normal. SOX10-inserted schwannomas exhibited histologic features characteristic of gastrointestinal schwannomas, including a microtrabecular arrangement of Schwann cells, peripheral lymphoid cuffs, and a lack of encapsulation. Both SOX10-inserted and SOX10-normal schwannomas demonstrated diffuse SOX10 immunoreactivity. The SOX10-inserted group was significantly associated with gastrointestinal locations (p < 0.001), older patients (p < 0.001), fusion negativity (p < 0.001), and larger tumor size (p = 0.013). Gene expression profiling of 44 cases revealed distinct transcriptomic profiles between primarily SOX10-inserted and SOX10-normal groups, with the latter group being classifiable into fusion-poor and fusion-enriched sub-clusters. This study highlights the genetic heterogeneity of schwannomas and suggests that SOX10 insertions play a pivotal role in the tumorigenesis of gastrointestinal schwannomas, distinctly separating them from non-gastrointestinal counterparts and contributing to their unique molecular profile.

Original languageEnglish
Pages (from-to)268-279
Number of pages12
JournalJournal of Pathology
Volume266
Issue number3
DOIs
Publication statusPublished - Jul 2025
Externally publishedYes

Keywords

  • NF2 mutation
  • SH3PXD2A::HTRA1 fusion
  • SOX10 insertion
  • gastrointestinal schwannoma
  • genetic heterogeneity
  • high mobility group box domain
  • histology
  • molecular pathogenesis
  • transcriptomic profile
  • whole exome sequencing

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

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