A Rare Adult Primary Intracranial Sarcoma, DICER1-Mutant Identified by Epigenomic Profiling: A Case Report

Author:

Marinelli Alfredo12,Cuomo Mariella34,Franca Raduan Ahmed5ORCID,Buonaiuto Michela34,Costabile Davide36ORCID,Pagano Cristina4ORCID,Trio Federica3,Montella Liliana7ORCID,Del Basso De Caro Maria Laura5ORCID,Visconti Roberta38ORCID,Chiariotti Lorenzo34,Della Monica Rosa34

Affiliation:

1. Operative Unit Neuroncology, University Federico II, 80131 Naples, Italy

2. Istituto di Ricerca e Cura a Carattere Scientifico (IRCCS), Neuromed Istituto Neurologico Mediterraneo (INM), 86077 Isernia, Italy

3. CEINGE, Advanceed Biotechnolgies “Franco Salvatore”, 80145 Naples, Italy

4. Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, 80131 Naples, Italy

5. Department of Advanced Biomedical Sciences, Pathology Section, University of Naples Federico II, 80131 Naples, Italy

6. SEMM-European School of Molecular Medicine, University of Naples, Federico II, 80145 Naples, Italy

7. ASL NA2 NORD, Oncology Operative Unit, “Santa Maria delle Grazie” Hospital, 80027 Pozzuoli, Italy

8. Institute for the Experimental Endocrinology and Oncology “G. Salvatore”, Italian National Council of Research, 80131 Naples, Italy

Abstract

Diagnoses of primary malignant mesenchymal brain tumors are a challenge for pathologists. Here, we report the case of a 52-year-old man with a primary brain tumor, histologically diagnosed as a high-grade glioma, not otherwise specified (NOS). The patient underwent two neurosurgeries in several months, followed by radiotherapy and chemotherapy. We re-examined the tumor samples by methylome profiling. Methylome analysis revealed an epi-signature typical of a primary intracranial sarcoma, DICER1-mutant, an extremely rare tumor. The diagnosis was confirmed by DNA sequencing that revealed a mutation in DICER1 exon 25. DICER1 mutations were not found in the patient’s blood cells, thus excluding an inherited DICER1 syndrome. The methylome profile of the DICER1 mutant sarcoma was then compared with that of a high-grade glioma, a morphologically similar tumor type. We found that several relevant regions were differentially methylated. Taken together, we report the morphological, epigenetic, and genetic characterization of the sixth described case of an adult primary intracranial sarcoma, DICER1-mutant to-date. Furthermore, this case report underscores the importance of methylome analysis to refine primary brain tumor diagnosis and to avoid misdiagnosis among morphologically similar subtypes.

Funder

Partenariato di Neuroscienze e Neurofarmacologia

Publisher

MDPI AG

Subject

General Neuroscience

Reference20 articles.

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2. Molecular tumor classification using DNA methylome analysis;Sill;Hum. Mol. Genet.,2020

3. DNA methylation-based classification of central nervous system tumours;Capper;Nature,2020

4. DNA methylation-based classification of sinonasal tumors;Jurmeister;Nat. Commun.,2022

5. Sarcoma classification by DNA methylation profiling;Koelsche;Nat. Commun.,2021

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