Immunophenotypic and molecular characterization of pancreatic neuroendocrine tumors producing serotonin.


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:
11 2022
Historique:
received: 16 02 2022
accepted: 12 05 2022
revised: 12 05 2022
pubmed: 24 6 2022
medline: 28 10 2022
entrez: 23 6 2022
Statut: ppublish

Résumé

Serotonin producing pancreatic neuroendocrine tumors (SP-PanNET) account for 0.58-1.4% of all pancreatic neuroendocrine tumors (PanNET). They may present with atypical symptoms, such as acute pancreatitis and are often radiologically characterized by main pancreatic duct dilatation. SP-PanNET are well differentiated neuroendocrine tumors (NET) distinct from classical PanNET by atypical serotonin secretion and abundant dense stroma deposition, like serotonin producing ileal NET leading in some cases to difficulties to reliably distinguish SP-PanNET from ileal NET metastases. The biology and molecular profile of SP-PanNET remain poorly characterized and the cell of origin within the pancreas is unclear. To address these questions, we analyzed a large cohort of SP-PanNET by immunohistochemistry (n = 29; ATRX, DAXX, MENIN, Islet1, PAX6, PDX1, ARX, CDX2), whole genome copy number array (Oncoscan™) and a large NGS panel (NovoPM™) (n = 10), FISH (n = 13) and RNA sequencing (n = 24) together with 21 ileal NET and 29 nonfunctioning PanNET (NF-PanNET). These analyses revealed a unique genomic profile with frequent isolated loss of chromosome 1 (14 cases-61%) and few pathogenic mutations (KMT2C in 2 cases, ARID1A in 1 case). Unsupervised RNAseq-based clustering showed that SP-PanNET were closer to NF-PanNET than ileal NET with an exclusive beta cell-like signature. SP-PanNET showed TGF-β pathway activation signatures associated with extracellular matrix remodeling and similar signature were reproduced in vitro when pancreatic stellate cells were exposed to serotonin. SP-PanNET immunohistochemical profile resemble that of ileal NET except for PDX1 and PAX6 expression to a lesser extend suggesting that these two markers may be useful to diagnose SP-PanNET. Taken together, this suggests that SP-PanNET are a very specific PanNET entity with a peculiar biology leading to the characteristic fibrotic aspect.

Identifiants

pubmed: 35739266
doi: 10.1038/s41379-022-01110-x
pii: S0893-3952(22)00238-1
doi:

Substances chimiques

Serotonin 333DO1RDJY
Transforming Growth Factor beta 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1713-1722

Informations de copyright

© 2022. The Author(s), under exclusive licence to United States & Canadian Academy of Pathology.

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Auteurs

Thomas Depoilly (T)

Université Paris Cité - APHP Hôpital Beaujon/Bichat, Department of Pathology, FHU MOSAIC, 100 Boulevard du Général Leclerc, 92110, Clichy, France.
Faculté de Médecine, Sorbonne-Université, 15 rue de l'Ecole de Médecine, 75006, Paris, France.

Raffaele Leroux (R)

INSERM U1149-Team 9, APHP-Hôpital Beaujon, 100 Boulevard du Général Leclerc, 92110, Clichy, France.

Dafne Andrade (D)

Department of Pathology, Grupo Fleury, São Paulo, Brasil.

Remy Nicolle (R)

INSERM U1149-Team 9, APHP-Hôpital Beaujon, 100 Boulevard du Général Leclerc, 92110, Clichy, France.

Marco Dioguardi Burgio (M)

Université Paris Cité - APHP Hôpital Beaujon, Department of Radiology, FHU MOSAIC, 100 Boulevard du Général Leclerc, 92110, Clichy, France.

Ilaria Marinoni (I)

Institute of Pathology, University of Bern, Murtenstrasse 31, 3008, Bern, Switzerland.

Safi Dokmak (S)

Université Paris Cité - APHP Hôpital Beaujon, Department of Hepatobiliary and Pancreatic Surgery, 100 Boulevard du Général Leclerc, 92110, Clichy, France.

Philippe Ruszniewski (P)

Université Paris Cité - APHP Hôpital Beaujon, Department of pancreatology, FHU MOSAIC, 100 Boulevard du Général Leclerc, 92110, Clichy, France.

Olivia Hentic (O)

Université Paris Cité - APHP Hôpital Beaujon, Department of pancreatology, FHU MOSAIC, 100 Boulevard du Général Leclerc, 92110, Clichy, France.

Valérie Paradis (V)

Université Paris Cité - APHP Hôpital Beaujon/Bichat, Department of Pathology, FHU MOSAIC, 100 Boulevard du Général Leclerc, 92110, Clichy, France.
INSERM U1149-Team 9, APHP-Hôpital Beaujon, 100 Boulevard du Général Leclerc, 92110, Clichy, France.

Louis De Mestier (L)

INSERM U1149-Team 9, APHP-Hôpital Beaujon, 100 Boulevard du Général Leclerc, 92110, Clichy, France.
Université Paris Cité - APHP Hôpital Beaujon, Department of pancreatology, FHU MOSAIC, 100 Boulevard du Général Leclerc, 92110, Clichy, France.

Aurel Perren (A)

Institute of Pathology, University of Bern, Murtenstrasse 31, 3008, Bern, Switzerland.

Anne Couvelard (A)

Université Paris Cité - APHP Hôpital Beaujon/Bichat, Department of Pathology, FHU MOSAIC, 100 Boulevard du Général Leclerc, 92110, Clichy, France.
INSERM U1149-Team 9, APHP-Hôpital Beaujon, 100 Boulevard du Général Leclerc, 92110, Clichy, France.

Jérôme Cros (J)

Université Paris Cité - APHP Hôpital Beaujon/Bichat, Department of Pathology, FHU MOSAIC, 100 Boulevard du Général Leclerc, 92110, Clichy, France. jerome.cros@aphp.fr.
INSERM U1149-Team 9, APHP-Hôpital Beaujon, 100 Boulevard du Général Leclerc, 92110, Clichy, France. jerome.cros@aphp.fr.

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