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DNA methylation as a new tool for the differential diagnosis between T-LBL and lymphocyte-rich thymoma.
Latiri, Mehdi; Belhocine, Mohamed; Smith, Charlotte; Garnier, Nathalie; Balducci, Estelle; Pinton, Antoine; Andrieu, Guillaume P; Bruneau, Julie; Spicuglia, Salvatore; Jamain, Stéphane; Latapie, Violaine; de Montpreville, Vincent Thomas; Chalabreysse, Lara; Marx, Alexander; Girard, Nicolas; Besse, Benjamin; Plass, Christoph; Gibault, Laure; Badoual, Cécile; Macintyre, Elizabeth; Asnafi, Vahid; Molina, Thierry Jo; Touzart, Aurore.
Affiliation
  • Latiri M; Laboratory of Onco-Hematology, Necker Children's Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Belhocine M; Université Paris Cité, CNRS, INSERM U1151, Institut Necker Enfants Malades (INEM), Paris, France.
  • Smith C; Aix-Marseille University, INSERM, TAGC, UMR1090, Equipe Labélisée Ligue Contre le Cancer, Marseille, France.
  • Garnier N; Department of Molecular Medicine,Al-Jawhara Centre for Molecular Medicine,Genetics, and Inherited Disorders, Arabian Gulf University, Manama, Bahrain.
  • Balducci E; Laboratory of Onco-Hematology, Necker Children's Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Pinton A; Université Paris Cité, CNRS, INSERM U1151, Institut Necker Enfants Malades (INEM), Paris, France.
  • Andrieu GP; Institute of Pediatric Hematology and Oncology, Hospices Civils de Lyon, Claude Bernard Lyon 1 University, Lyon, France.
  • Bruneau J; Laboratory of Onco-Hematology, Necker Children's Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Spicuglia S; Université Paris Cité, CNRS, INSERM U1151, Institut Necker Enfants Malades (INEM), Paris, France.
  • Jamain S; Laboratory of Onco-Hematology, Necker Children's Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Latapie V; Université Paris Cité, CNRS, INSERM U1151, Institut Necker Enfants Malades (INEM), Paris, France.
  • de Montpreville VT; Laboratory of Onco-Hematology, Necker Children's Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Chalabreysse L; Université Paris Cité, CNRS, INSERM U1151, Institut Necker Enfants Malades (INEM), Paris, France.
  • Marx A; Department of Pathology, Hôpital Necker-Enfants Malades, Université Paris-Cité, Paris, France.
  • Girard N; Aix-Marseille University, INSERM, TAGC, UMR1090, Equipe Labélisée Ligue Contre le Cancer, Marseille, France.
  • Besse B; Univ Paris Est Créteil, INSERM, IMRB, Translational Neuropsychiatry, Créteil, France.
  • Plass C; Univ Paris Est Créteil, INSERM, IMRB, Translational Neuropsychiatry, Créteil, France.
  • Gibault L; Department of Pathology, Marie-Lannelongue Hospital, Le Plessis-Robinson, France.
  • Badoual C; Department of Pathology, Groupe Hospitalier Est, Hospices Civils de Lyon, Bron, France.
  • Macintyre E; Institute of Pathology, University Medical Center Göttingen, Göttingen, Germany.
  • Asnafi V; Thorax Institute Curie Montsouris, Paris, France.
  • Molina TJ; Universite de Versailles Saint Quentin (UVSQ), Paris-Saclay University, Versailles, France.
  • Touzart A; Department of Cancer Medicine, Gustave Roussy Cancer Campus, Villejuif, France.
J Pathol ; 264(3): 284-292, 2024 Nov.
Article de En | MEDLINE | ID: mdl-39329449
ABSTRACT
T-lymphoblastic lymphoma (T-LBL) and thymoma are two rare primary tumors of the thymus deriving either from T-cell precursors or from thymic epithelial cells, respectively. Some thymoma subtypes (AB, B1, and B2) display numerous reactive terminal deoxynucleotidyl transferase-positive (TdT+) T-cell precursors masking epithelial tumor cells. Therefore, the differential diagnosis between T-LBL and TdT+ T-lymphocyte-rich thymoma could be challenging, especially in the case of needle biopsy. To distinguish between T-LBL and thymoma-associated lymphoid proliferations, we analyzed the global DNA methylation using two different technologies, namely MeDIP array and EPIC array, in independent samples series [17 T-LBLs compared with one TdT+ lymphocyte-rich thymoma (B1 subtype) and three normal thymi, and seven lymphocyte-rich thymomas compared with 24 T-LBLs, respectively]. In unsupervised principal component analysis (PCA), T-LBL and thymoma samples clustered separately. We identified differentially methylated regions (DMRs) using MeDIP-array and EPIC-array datasets and nine overlapping genes between the two datasets considering the top 100 DMRs including ZIC1, TSHZ2, CDC42BPB, RBM24, C10orf53, and MACROD2. In order to explore the DNA methylation profiles in larger series, we defined a classifier based on these six differentially methylated gene promoters, developed an MS-MLPA assay, and demonstrated a significant differential methylation between thymomas (hypomethylated; n = 48) and T-LBLs (hypermethylated; n = 54) (methylation ratio median 0.03 versus 0.66, respectively; p < 0.0001), with MACROD2 methylation status the most discriminating. Using a machine learning strategy, we built a prediction model trained with the EPIC-array dataset and defined a cumulative score taking into account the weight of each feature. A score above or equal to 0.4 was predictive of T-LBL and conversely. Applied to the MS-MLPA dataset, this prediction model accurately predicted diagnoses of T-LBL and thymoma. © 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Thymome / Tumeurs du thymus / Méthylation de l'ADN / Leucémie-lymphome lymphoblastique à précurseurs T Limites: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Langue: En Journal: J Pathol Année: 2024 Type de document: Article Pays d'affiliation: France Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Thymome / Tumeurs du thymus / Méthylation de l'ADN / Leucémie-lymphome lymphoblastique à précurseurs T Limites: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Langue: En Journal: J Pathol Année: 2024 Type de document: Article Pays d'affiliation: France Pays de publication: Royaume-Uni