Gene Expression Profiling of Lung Atypical Carcinoids and Large Cell Neuroendocrine Carcinomas Identifies Three Transcriptomic Subtypes with Specific Genomic Alterations.


Journal

Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235

Informations de publication

Date de publication:
09 2019
Historique:
received: 11 01 2019
revised: 25 03 2019
accepted: 06 05 2019
pubmed: 16 5 2019
medline: 18 8 2020
entrez: 16 5 2019
Statut: ppublish

Résumé

DNA mutational profiling showed that atypical carcinoids (ACs) share alterations with large cell neuroendocrine carcinomas (LCNECs). Transcriptomic studies suggested that LCNECs are composed of two subtypes, one of which shares molecular anomalies with SCLC. The missing piece of information is the transcriptomic relationship between ACs and LCNECs, as a direct comparison is lacking in the literature. Transcriptomic and genomic alterations were investigated by next-generation sequencing in a discovery set of 14 ACs and 14 LCNECs and validated on 21 ACs and 18 LCNECs by using custom gene panels and immunohistochemistry for Men1 and Rb1. A 58-gene signature distinguished three transcriptional clusters. Cluster 1 comprised 20 LCNECs and one AC harboring concurrent inactivation of tumor protein p53 gene (TP53) and retinoblastoma 1 gene (RB1) in the absence of menin 1 gene (MEN1) mutations; all cases lacked Rb1 nuclear immunostaining. Cluster 3 included 20 ACs and four LCNECs lacking RB1 alterations and having frequent MEN1 (37.5%) and TP53 mutations (16.7%); menin nuclear immunostaining was lost in 75% of cases. Cluster 2 included 14 ACs and eight LCNECs showing intermediate features: TP53, 40.9%; MEN1, 22.7%; and RB1, 18.2%. Patients in cluster C1 had a shorter cancer-specific survival than did patients in C2 or C3. ACs and LCNECs comprise three different and clinically relevant molecular diseases, one AC-enriched group in which MEN1 inactivation plays a major role, one LCNEC-enriched group whose hallmark is RB1 inactivation, and one mixed group with intermediate molecular features. These data support a progression of malignancy that may be traced by using combined molecular and immunohistochemical analysis.

Identifiants

pubmed: 31085341
pii: S1556-0864(19)30366-1
doi: 10.1016/j.jtho.2019.05.003
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1651-1661

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.

Auteurs

Michele Simbolo (M)

Department of Diagnostics and Public Health, Section of Anatomical Pathology, University and Hospital Trust of Verona, Verona, Italy.

Stefano Barbi (S)

Department of Diagnostics and Public Health, Section of Anatomical Pathology, University and Hospital Trust of Verona, Verona, Italy.

Matteo Fassan (M)

ARC-Net Research Centre, University and Hospital Trust of Verona, Verona, Italy.

Andrea Mafficini (A)

ARC-Net Research Centre, University and Hospital Trust of Verona, Verona, Italy.

Greta Ali (G)

Department of Surgical, Medical, Molecular Pathology and Critical Area, University of Pisa, AOU Pisana, Pisa, Italy.

Caterina Vicentini (C)

Department of Diagnostics and Public Health, Section of Anatomical Pathology, University and Hospital Trust of Verona, Verona, Italy; ARC-Net Research Centre, University and Hospital Trust of Verona, Verona, Italy.

Nicola Sperandio (N)

Department of Diagnostics and Public Health, Section of Anatomical Pathology, University and Hospital Trust of Verona, Verona, Italy; ARC-Net Research Centre, University and Hospital Trust of Verona, Verona, Italy.

Vincenzo Corbo (V)

Department of Diagnostics and Public Health, Section of Anatomical Pathology, University and Hospital Trust of Verona, Verona, Italy.

Borislav Rusev (B)

ARC-Net Research Centre, University and Hospital Trust of Verona, Verona, Italy.

Luca Mastracci (L)

Department of Surgical and Diagnostic Sciences, University of Genoa and IRCCS S. Martino-IST University Hospital, Genoa, Italy.

Federica Grillo (F)

Department of Surgical and Diagnostic Sciences, University of Genoa and IRCCS S. Martino-IST University Hospital, Genoa, Italy.

Sara Pilotto (S)

Department of Medicine, Section of Medical Oncology, University and Hospital Trust of Verona, Verona, Italy.

Giuseppe Pelosi (G)

Department of Oncology and Hemato-Oncology, University of Milan, and Inter-Hospital Pathology Division, IRCCS MultiMedica, Milan, Italy.

Serena Pelliccioni (S)

Department of Surgical, Medical, Molecular Pathology and Critical Area, University of Pisa, AOU Pisana, Pisa, Italy.

Rita T Lawlor (RT)

ARC-Net Research Centre, University and Hospital Trust of Verona, Verona, Italy.

Giampaolo Tortora (G)

Department of Medicine, Section of Medical Oncology, University and Hospital Trust of Verona, Verona, Italy; Comprehensive Cancer Center, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy; Sacred Hearth Catholic University, Rome, Italy.

Gabriella Fontanini (G)

Department of Surgical, Medical, Molecular Pathology and Critical Area, University of Pisa, AOU Pisana, Pisa, Italy.

Marco Volante (M)

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

Aldo Scarpa (A)

Department of Diagnostics and Public Health, Section of Anatomical Pathology, University and Hospital Trust of Verona, Verona, Italy; ARC-Net Research Centre, University and Hospital Trust of Verona, Verona, Italy. Electronic address: aldo.scarpa@univr.it.

Emilio Bria (E)

Comprehensive Cancer Center, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy; Sacred Hearth Catholic University, Rome, Italy.

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Classifications MeSH