A Spatially Resolved Dark- versus Light-Zone Microenvironment Signature Subdivides Germinal Center-Related Aggressive B Cell Lymphomas.

Cancer Cancer Systems Biology Transcriptomics

Journal

iScience
ISSN: 2589-0042
Titre abrégé: iScience
Pays: United States
ID NLM: 101724038

Informations de publication

Date de publication:
23 Oct 2020
Historique:
received: 22 05 2020
revised: 23 07 2020
accepted: 10 09 2020
entrez: 21 10 2020
pubmed: 22 10 2020
medline: 22 10 2020
Statut: epublish

Résumé

We applied digital spatial profiling for 87 immune and stromal genes to lymph node germinal center (GC) dark- and light-zone (DZ/LZ) regions of interest to obtain a differential signature of these two distinct microenvironments. The spatially resolved 53-genes signature, comprising key genes of the DZ mutational machinery and LZ immune and mesenchymal milieu, was applied to the transcriptomes of 543 GC-related diffuse large B cell lymphomas and double-hit (DH) lymphomas. According to the DZ/LZ signature, the GC-related lymphomas were sub-classified into two clusters. The subgroups differed in the distribution of DH cases and survival, with most DH displaying a distinct DZ-like profile. The clustering analysis was also performed using a 25-genes signature composed of genes positively enriched in the non-B, stromal sub-compartments, for the first time achieving DZ/LZ discrimination based on stromal/immune features. The report offers new insight into the GC microenvironment, hinting at a DZ microenvironment of origin in DH lymphomas.

Identifiants

pubmed: 33083730
doi: 10.1016/j.isci.2020.101562
pii: S2589-0042(20)30754-9
pmc: PMC7522121
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101562

Informations de copyright

© 2020 The Author(s).

Déclaration de conflit d'intérêts

A.V. works as Scientist for NanoString Technologies Inc. The remaining authors have nothing to disclose.

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Auteurs

Claudio Tripodo (C)

Tumor Immunology Unit, University of Palermo, Corso Tukory 211, 90134, Palermo, Italy.
Tumor and Microenvironment Histopathology Unit, IFOM, the FIRC Institute of Molecular Oncology, Milan, Italy.

Federica Zanardi (F)

Bioinformatics Core Unit, IFOM, FIRC Institute of Molecular Oncology, Milan, Italy.

Fabio Iannelli (F)

Bioinformatics Core Unit, IFOM, FIRC Institute of Molecular Oncology, Milan, Italy.

Saveria Mazzara (S)

Hematopathology Unit, European Institute of Oncology, Milan, Italy.

Mariella Vegliante (M)

Hematology and Cell Therapy Unit, IRCCS-Istituto Tumori "Giovanni Paolo II", Bari, Italy.

Gaia Morello (G)

Tumor Immunology Unit, University of Palermo, Corso Tukory 211, 90134, Palermo, Italy.

Arianna Di Napoli (A)

Pathology Unit, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.

Alessandro Mangogna (A)

Tumor Immunology Unit, University of Palermo, Corso Tukory 211, 90134, Palermo, Italy.

Fabio Facchetti (F)

Pathology Unit, University of Brescia, Brescia, Italy.

Sabina Sangaletti (S)

Molecular Immunology Unit, National Cancer Institute, Milan, Italy.

Claudia Chiodoni (C)

Molecular Immunology Unit, National Cancer Institute, Milan, Italy.

Alison VanShoiack (A)

NanoString Technologies, Inc., Seattle, WA, USA.

Anand D Jeyasekharan (AD)

Department of Hematology-Oncology, National University Cancer Institute, Singapore, Singapore.

Stefano Casola (S)

Genetics of B Cells and Lymphomas Unit, IFOM, the FIRC Institute of Molecular Oncology, Milan, Italy.

Mario P Colombo (MP)

Molecular Immunology Unit, National Cancer Institute, Milan, Italy.

Maurilio Ponzoni (M)

Vita-Salute San Raffaele University Milan, Milan, Italy.
Pathology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Stefano A Pileri (SA)

Hematopathology Unit, European Institute of Oncology, Milan, Italy.

Classifications MeSH