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March 5, 2026Acta Neuropathologica Communications0 citationsOpen Access

CUX1::MET fusion defines an indolent subtype of diffuse low-grade glioma, MAPK pathway–altered

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HNHiroaki NagashimaYTYasuhide TakeuchiNJNaoe Jimbo

Key Points

  • This research investigates the biological significance of the CUX1::MET fusion in diffuse low-grade glioma altered by the MAPK pathway.
  • Case report of a 25-year-old woman with a right temporal lobe tumor
  • Histological examination revealing oligodendroglioma-like features
  • Molecular analysis for genetic alterations, specifically a CUX1::MET fusion
  • Identified a novel CUX1::MET fusion that activates the MAPK pathway
  • The tumor exhibited low-grade features and a low proliferative index
  • Despite MET alteration, the glioma displayed an indolent clinical course over 15 years

Abstract

Diffuse low-grade glioma, MAPK pathway–altered (DLGG–MAPK), is a recently defined tumor entity characterized by genetic alterations activating the MAPK signaling cascade. While BRAF and FGFR alterations are most frequently reported, the biological and clinical significance of other MAPK-activating events remains poorly understood. We report a 25-year-old woman with a right temporal lobe tumor harboring a novel CUX1::MET fusion. The lesion was initially detected at age 10 during neuroimaging performed for a transient headache and subsequently followed an indolent clinical course for approximately 15 years before manifesting with acute hemorrhage. Histologically, the tumor showed diffuse infiltration with oligodendroglioma-like morphology, absence of high-grade features, and a low proliferative index. Molecular analysis identified an in-frame CUX1::MET fusion retaining the MET kinase domain, resulting in exon 14 skipping and activation of the MAPK pathway. Despite the presence of a MET alteration typically associated with aggressive tumors, the lesion demonstrated prolonged indolence and low-grade biological behavior. To our knowledge, this is the first case report demonstrating the presence of a CUX1::MET fusion in DLLG-MAPK. This case expands the molecular spectrum of DLGG–MAPK and provides novel insight into the biological heterogeneity of MET-driven gliomas, suggesting that MET fusion alone is insufficient to confer high-grade behavior in this tumor context.

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Cite This Study

Nagashima et al. (2026) studied this question.

synapsesocial.com/papers/69a91e1fd6127c7a504c1b49https://doi.org/10.1186/s40478-026-02271-5
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Also Consider

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  1. 1CLIP2::MET fusion identifies a molecularly distinct glioneuronal tumor2026
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  5. 5Early‐Onset Medullocervical Low‐Grade Glioma With <scp>FGFR1</scp> Mutation and Leptomeningeal Spread in an Infant: A Case Report2026