Evidence map›Paper›PMID 32516416›Full record

ArticleBlood advances2020

Gene expression profiling of gray zone lymphoma.

Clémentine Sarkozy, Lauren Chong, Katsuyoshi Takata, Elizabeth A Chavez, Tomoko Miyata-Takata, Gerben Duns, Adèle Telenius, Merrill Boyle, Graham W Slack, Camille Laurent and 10 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.8field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
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  9. [Lymphomas in children and adolescents].Pathologie (Heidelberg, Germany) · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 5 institutions in 3 countries.

Clémentine SarkozyINSERM Unité Mixte de Recherche (UMR)-S1052, Centre National de la Recherche UMR 5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Lauren ChongCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Katsuyoshi TakataCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Elizabeth A ChavezCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Tomoko Miyata-TakataCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Gerben DunsCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Adèle TeleniusCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Merrill BoyleCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Graham W SlackCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Camille LaurentInstitut Universitaire du Cancer-Oncopole de Toulouse, Centre Hospitalier Universitaire Toulouse, INSERM U.1037, Centre de Recherche en Cancerologie de Toulouse-Purpan, Toulouse, France.
Pedro FarinhaCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Thierry J MolinaPathology Department, Necker Enfants Malades Hospital, Université Paris Descartes, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Christiane Copie-BergmanPathology Department, Henri Mondor-Albert Chennevier Hospital, AP-HP, Paris Est-Créteil (UPEC) University, UMR-S 955, INSERM, Créteil, France.
Diane DamotteDépartement de Pathologie, Groupe Hospitalier Cochin, AP-HP, Paris Descartes University-Sorbonne, Paris, France.
Gilles A SallesINSERM Unité Mixte de Recherche (UMR)-S1052, Centre National de la Recherche UMR 5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Anja MottokInstitute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany; and.
Kerry J SavageCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
David W ScottCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Alexandra Traverse-GlehenINSERM Unité Mixte de Recherche (UMR)-S1052, Centre National de la Recherche UMR 5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Christian SteidlCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Spinal Cord Injury BC · CAInserm · FRDélégation Paris 5 · FRHôpital Necker-Enfants Malades · FRUniversität Ulm · DE

Funding

CIHR
6 · The paper itself

Abstract

Gray zone lymphoma (GZL), a B-cell lymphoma with features intermediate between large B-cell lymphoma (LBCL) and classic Hodgkin lymphoma (cHL), is a rare and poorly defined entity. Alongside GZL, a subset of Epstein-Barr virus (EBV)-positive diffuse large B-cell lymphoma (DLBCL) has been described with polymorphic/GZL-like morphology (polymorphic-EBV-L). To fill the important gap in our understanding of the pathogenic process underlying these entities, we performed a gene expression study of a large international cohort of GZL and polymorphic-EBV-L, combined with cHL and primary mediastinal large B-cell lymphoma (PMBCL) cases. In an unsupervised principal component analysis, GZL cases presented with intermediate scores in a spectrum between cHL and PMBCL, whereas polymorphic-EBV-L clustered distinctly. The main biological pathways underlying the GZL spectrum were related to cell cycle, reflecting tumor cell content, and extracellular matrix signatures related to the cellular tumor microenvironment. Differential expression analysis and phenotypic characterization of the tumor microenvironment highlighted the predominance of regulatory macrophages in GZL compared with cHL and PMBCL. Two distinct subtypes of GZL were distinguishable that were phenotypically reminiscent of PMBCL and DLBCL, and we observed an association of PMBCL-type GZL with clinical presentation in the "thymic" anatomic niche. In summary, gene expression profiling (GEP) enabled us to add precision to the GZL spectrum, describe the biological distinction compared with polymorphic-EBV-L, and distinguish cases with and without thymic involvement as 2 subgroups of GZL, namely PMBCL-like and DLBCL-like GZL.

Indexed as

Epstein-Barr Virus InfectionsGene Expression ProfilingHodgkin DiseaseLymphoma, Large B-Cell, DiffuseFemaleHerpesvirus 4, HumanHumansMaleMiddle AgedTumor Microenvironment

Identifiers

PMID32516416
PMCPMC7284085
OpenAlexW3033237799

What OpenQuestion holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.