Michel Kalamarides1,2,3, Gaëlle Pierron4, Caroline Apra5,6,7, Delphine Guillemot4, Eléonore Frouin4, Corinne Bouvier8, Karima Mokhtari2,3,9. 1. Sorbonne Université, Paris, France. 2. Department of Neurosurgery, Pitié-Salpêtrière Hospital, 47-83 bd de l'Hôpital, 75013, Paris, France. 3. Paris Brain Institute, INSERM U1127, CNRS, UMR7225, 47-83 bd de l'Hôpital, 75013, Paris, France. 4. Pole of Diagnostic and Theranostic Medecine, Institut Curie, 26 rue d'Ulm, 75005, Paris, France. 5. Sorbonne Université, Paris, France. caroline.apra@neurochirurgie.fr. 6. Department of Neurosurgery, Pitié-Salpêtrière Hospital, 47-83 bd de l'Hôpital, 75013, Paris, France. caroline.apra@neurochirurgie.fr. 7. Paris Brain Institute, INSERM U1127, CNRS, UMR7225, 47-83 bd de l'Hôpital, 75013, Paris, France. caroline.apra@neurochirurgie.fr. 8. Department of Pathology, APHM, CHU Timone, INSERM, MMG Aix Marseille University, Marseille, France. 9. Department of Neuropathology, Pitié-Salpêtrière Hospital, 47-83 bd de l'Hôpital, 75013, Paris, France.
Abstract
INTRODUCTION: Meningeal solitary fibrous tumors (SFT), like all SFT, are defined by NAB2-STAT6 fusion and share clinicopathologic similarities with meningiomas, the most frequent meningeal tumors. Our aim is to establish the molecular identity of meningeal SFT and seek molecular prognostic factors. METHODS: RNA sequencing and whole exome sequencing were performed in STAT6-positive SFT and grade 2-3 meningiomas, and data concerning other soft tissues tumors was obtained from the local database. Uniform manifold approximation and projection, individual gene expression and Gene Set Enrichment Analysis were performed. RESULTS: RNA clustering shows that SFT share a common molecular signature, different from any other type of tumoral tissue. Meningeal SFT aggregate with other SFT, with no clinical or histological subgroup. Comparison of genes expressions suggests significant over-expressions of ZIC2, ZIC3, ZIC5, GABBR2, TP53 in CNS-SFT. The pathogenic TP53 c.743G>T variant, previously undescribed in SFT, was found in one sample of meningeal SFT during malignant progression. CONCLUSIONS: Meningeal SFT are molecular counterparts of extra-meningeal SFT, completely separate from meningiomas. They might develop from the same tissues and benefit from the same treatments as SFT.
INTRODUCTION: Meningeal solitary fibrous tumors (SFT), like all SFT, are defined by NAB2-STAT6 fusion and share clinicopathologic similarities with meningiomas, the most frequent meningeal tumors. Our aim is to establish the molecular identity of meningeal SFT and seek molecular prognostic factors. METHODS: RNA sequencing and whole exome sequencing were performed in STAT6-positive SFT and grade 2-3 meningiomas, and data concerning other soft tissues tumors was obtained from the local database. Uniform manifold approximation and projection, individual gene expression and Gene Set Enrichment Analysis were performed. RESULTS: RNA clustering shows that SFT share a common molecular signature, different from any other type of tumoral tissue. Meningeal SFT aggregate with other SFT, with no clinical or histological subgroup. Comparison of genes expressions suggests significant over-expressions of ZIC2, ZIC3, ZIC5, GABBR2, TP53 in CNS-SFT. The pathogenic TP53 c.743G>T variant, previously undescribed in SFT, was found in one sample of meningeal SFT during malignant progression. CONCLUSIONS: Meningeal SFT are molecular counterparts of extra-meningeal SFT, completely separate from meningiomas. They might develop from the same tissues and benefit from the same treatments as SFT.
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