PAX8-GLIS3 gene fusion is a pathognomonic genetic alteration of hyalinizing trabecular tumors of the thyroid.


Journal

Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
ISSN: 1530-0285
Titre abrégé: Mod Pathol
Pays: United States
ID NLM: 8806605

Informations de publication

Date de publication:
12 2019
Historique:
received: 13 04 2019
accepted: 29 05 2019
revised: 28 05 2019
pubmed: 6 7 2019
medline: 18 8 2020
entrez: 6 7 2019
Statut: ppublish

Résumé

The hyalinizing trabecular adenoma/tumor is a rare and poorly characterized follicular-derived thyroid neoplasm recently shown to harbor recurrent PAX8-GLIS1 or PAX8-GLIS3 gene fusions. Here we sought to define the repertoire of genetic alterations of hyalinizing trabecular tumors, and whether PAX8-GLIS3 fusions are pathognomonic for hyalinizing trabecular tumors. A discovery series of eight hyalinizing trabecular tumors was subjected to RNA-sequencing (n = 8), whole-exome sequencing (n = 3) or targeted massively parallel sequencing (n = 5). No recurrent somatic mutations or copy number alterations were identified in hyalinizing trabecular tumor, whereas RNA-sequencing revealed the presence of a recurrent genetic rearrangement involving PAX8 (2q14.1) and GLIS3 (9p24.2) genes in all cases. In this in-frame fusion gene, which comprised exons 1-2 of PAX8 and exons 3-11 of GLIS3, GLIS3 is likely placed under the regulation of PAX8. Reverse transcription RT-PCR and/or fluorescence in situ hybridization analyses of a validation series of 26 hyalinizing trabecular tumors revealed that the PAX8-GLIS3 gene fusion was present in all hyalinizing trabecular tumors (100%). No GLIS1 rearrangements were identified. Conversely, no PAX8-GLIS3 gene fusions were detected in a cohort of 237 control thyroid neoplasms, including 15 trabecular thyroid lesions highly resembling hyalinizing trabecular tumor from a morphological standpoint, as well as trabecular/solid follicular adenomas, solid/trabecular variants of papillary carcinoma, and Hurthle cell adenomas or carcinomas. Our data provide evidence to suggest that the PAX8-GLIS3 fusion is pathognomonic for hyalinizing trabecular tumors, and that the presence of the PAX8-GLIS3 fusion in thyroid neoplasms may be used as an ancillary marker for the diagnosis of hyalinizing trabecular tumor, thereby avoiding overtreatment in case of misdiagnoses with apparently similar malignant tumors.

Identifiants

pubmed: 31273314
doi: 10.1038/s41379-019-0313-x
pii: S0893-3952(22)00967-X
pmc: PMC7442035
mid: NIHMS1609698
doi:

Substances chimiques

DNA-Binding Proteins 0
GLIS3 protein, human 0
Oncogene Proteins, Fusion 0
PAX8 Transcription Factor 0
PAX8 protein, human 0
Repressor Proteins 0
Trans-Activators 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1734-1743

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

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Auteurs

Caterina Marchiò (C)

Pathology Division, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.
Department of Medical Sciences, University of Turin, Torino, Italy.

Arnaud Da Cruz Paula (A)

Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Rodrigo Gularte-Merida (R)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Thais Basili (T)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Alissa Brandes (A)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Edaise M da Silva (EM)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Catarina Silveira (C)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Lorenzo Ferrando (L)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Internal Medicine, University of Genova, Genova, Italy.

Jasna Metovic (J)

Department of Oncology, University of Turin, at Città della Salute Hospital, Torino, Italy.

Francesca Maletta (F)

Department of Oncology, University of Turin, at Città della Salute Hospital, Torino, Italy.

Laura Annaratone (L)

Pathology Division, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.
Department of Medical Sciences, University of Turin, Torino, Italy.

Fresia Pareja (F)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Brian P Rubin (BP)

Department of Pathology, Cleveland Clinic, Cleveland, OH, USA.

Aaron P Hoschar (AP)

Department of Pathology, Cleveland Clinic, Cleveland, OH, USA.

Giovanni De Rosa (G)

Pathology Division, Mauriziano Hospital, Torino, Italy.

Stefano La Rosa (S)

Service of Clinical Pathology, Lausanne University Hospital, Institute of Pathology, Lausanne, Switzerland.

Massimo Bongiovanni (M)

Service of Clinical Pathology, Lausanne University Hospital, Institute of Pathology, Lausanne, Switzerland.

Bibianna Purgina (B)

Department of Pathology and Laboratory Medicine, Ottawa Hospital, ON, Canada.

Simonetta Piana (S)

Pathology Unit, Arcispedale Santa Maria Nuova, Azienda USL-IRCCS, Reggio Emilia, Italy.

Marco Volante (M)

San Luigi Gonzaga Hospital and Department of Oncology, University of Turin, Orbassano, Italy.

Britta Weigelt (B)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Jorge S Reis-Filho (JS)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA. reisfilj@mskcc.org.
Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA. reisfilj@mskcc.org.

Mauro Papotti (M)

Department of Oncology, University of Turin, at Città della Salute Hospital, Torino, Italy. mauro.papotti@unito.it.

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