Evidence map›Paper›PMID 42675868›Full record

ArticleThe Journal of pathology2026

Comprehensive genomic profiling of mucosal melanoma reveals novel fusion transcripts and dysregulation of cell-cycle, MAPK, and PI3K pathways.

Matilde Monti, Martina Brigida Romanello, Luca Agnelli, Matteo Orlandi, Luca Bertoli, Sara Picinoli, Irene Pezzali, Giulio Eugenio Mandelli, Daniela Medicina, Giovanni Ribaudo and 12 more

Abstract read
In one paragraph

Article in The Journal of pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Matilde MontiDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Martina Brigida RomanelloDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Luca AgnelliDepartment of Diagnostic Innovation, Pathology Unit 2, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
Matteo OrlandiDepartment of Biotechnology, University of Verona, Verona, Italy.
Luca BertoliDepartment of Biotechnology, University of Verona, Verona, Italy.
Sara PicinoliDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Irene PezzaliDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Giulio Eugenio MandelliUnit of Pathology, Department of Molecular and Translational Medicine, University of Brescia - 'ASST Spedali Civili di Brescia', Brescia, Italy.
Daniela MedicinaUnit of Pathology, Department of Molecular and Translational Medicine, University of Brescia - 'ASST Spedali Civili di Brescia', Brescia, Italy.
Giovanni RibaudoDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Adele BusicoDepartment of Diagnostic Innovation, Pathology Unit 2, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
Elena ConcaDepartment of Diagnostic Innovation, Pathology Unit 2, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
Vilma PellegriniUnit of Pathology, Department of Molecular and Translational Medicine, University of Brescia - 'ASST Spedali Civili di Brescia', Brescia, Italy.
Piera BalzariniDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Daniele GallucciDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Anna Di MatteoIstituto di Genetica Molecolare 'Luigi Luca Cavalli-Sforza', Consiglio Nazionale delle Ricerche, Pavia, Italy.
Davide LombardiUnit of Otorhinolaryngology - Head and Neck Surgery, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
Claudia GhignaIstituto di Genetica Molecolare 'Luigi Luca Cavalli-Sforza', Consiglio Nazionale delle Ricerche, Pavia, Italy.
Giancarlo PruneriDepartment of Diagnostic Innovation, Pathology Unit 2, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
Alessandra GianoncelliDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Marzia RossatoDepartment of Biotechnology, University of Verona, Verona, Italy.
William VermiDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.ORCID https://orcid.org/0000-0002-2291-2997

Funding

Associazione Italiana per la Ricerca sul Cancro IG-23179Associazione Italiana per la Ricerca sul Cancro IG-29002Fondazione Umberto VeronesiPRIN 2022 PNRR P2022S5JWBValentino Morbio' Fondazione Spedali Civili Brescia
6 · The paper itself

Abstract

Mucosal melanomas (MMs) are rare, aggressive cancers with poor outcomes and limited response to standard therapies. A significant knowledge gap exists regarding their genomic landscape and corresponding druggable targets. This study explores this issue through a multi-omic analysis, including whole exome-, RNA-, and targeted sequencing, of unique sinonasal mucosal melanoma (SN-MM) cell lines. SN-MM cell lines showed a low tumour mutational burden and low genomic instability, suggesting that their DNA repair mechanisms are largely intact. However, they exhibited a high prevalence of structural variants, likely from catastrophic genomic events. We also found novel, clinically actionable variants, including oncogenic fusion transcripts. Key findings, such as fusion transcripts and single-nucleotide variants, were validated on diagnostic biopsies. Moreover, using a break-apart FISH assay, we identified BRAF rearrangements as recurrent events in MM, supporting their biological relevance. The MAPK pathway was found to have a significant functional role, sustained by variants such as BRAF p.Asn581Ser, NRAS p.Gly12Asp, and the MKRN1::BRAF fusion. This pathway activation was effectively inhibited by the MEK inhibitor trametinib. This genomic and functional profiling unveiled novel molecular hubs in MM. The findings propose that MEK inhibitors may represent a relevant therapeutic option for BRAF fusions and non-V600 BRAF mutant tumours, providing a novel strategy for this challenging disease. Further molecular and functional validation of novel variants, and particularly of BRAF rearrangements, may reveal additional clinically relevant therapeutic targets. © 2026 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

Indexed as

Cell CycleMelanomaNasal MucosaNose NeoplasmsPhosphatidylinositol 3-KinasesCell Line, TumorGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMAP Kinase Signaling SystemMutationProtein Kinase InhibitorsProto-Oncogene Proteins B-rafPyridonesPyrimidinonesSignal TransductionBRAF protein, humanPhosphatidylinositol 3-KinasesProtein Kinase InhibitorsProto-Oncogene Proteins B-rafPyridonesPyrimidinonestrametinibfusion transcriptsgenomic landscapeMAPK pathwaymucosal melanomassingle‐nucleotide variantssinonasal melanomastructural variantstrametinib

Identifiers

PMID42675868
PMCPMC13635605

What Socratic holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.