Evidence map›Paper›PMID 30206415›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2019

Transcriptional analysis distinguishes breast implant-associated anaplastic large cell lymphoma from other peripheral T-cell lymphomas.

Arianna Di Napoli, Loris De Cecco, Pier Paolo Piccaluga, Mohsen Navari, Valeria Cancila, Claudia Cippitelli, Giuseppina Pepe, Gianluca Lopez, Francesca Monardo, Antonella Bianchi and 5 more

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In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
8.3field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Guideline
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  9. Extranodal T- and NK-cell lymphomas.Virchows Archiv : an international journal of pathology · 2023
    Review
  10. Article
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  16. Genetic profiling and biomarkers in peripheral T-cell lymphomas: current role in the diagnostic work-up.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Review
  17. Article
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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

15 authors at 12 institutions in 3 countries.

Arianna Di NapoliDepartment of Clinical and Molecular Medicine, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy. arianna.dinapoli@uniroma1.it.ORCID http://orcid.org/0000-0002-3159-5380
Loris De CeccoIntegrated Biology Platform, Department of Applied Research and Technology Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Pier Paolo PiccalugaDepartment of Experimental, Diagnostic and Experimental Medicine, Bologna University School of Medicine, Bologna, Italy.ORCID http://orcid.org/0000-0002-9432-0595
Mohsen NavariResearch Center of Advanced Technologies in Medicine, Torbat Heydariyeh University of Medical Sciences, Torbat Heydariyeh, Iran.
Valeria CancilaTumor Immunology Unit, Dipartimento per la Promozione della Salute e Materno Infantile "G. D'Alessandro", University of Palermo, Palermo, Italy.
Claudia CippitelliDepartment of Clinical and Molecular Medicine, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
Giuseppina PepeDepartment of Clinical and Molecular Medicine, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
Gianluca LopezDepartment of Clinical and Molecular Medicine, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
Francesca MonardoPathology Unit, San Giovanni Addolorata Hospital, Roma, Italy.
Antonella BianchiPathology Unit, University Hospital Campus Bio-Medico, Rome, Italy.
Emanuele Stefano Giovanni D'AmoreInstitute of Pathology, San Bortolo Hospital, Vicenza, Italy.
Umberto GianelliHematopathology Unit, Department of Physiopathology and Transplantation, IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
Fabio FacchettiPathology Section, Department of Molecular and Translational Medicine, University-Spedali Civili of Brescia, Spedali Civili di Brescia, Brescia, Italy.
Emilio BertiDermatology Unit, Department of Physiopathology and Transplantation, IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
Govind BhagatDepartment of Pathology and Cell Biology, Columbia University Medical Center, New York Presbyterian Hospital, New York, NY, USA. gb96@cumc.columbia.edu.ORCID http://orcid.org/0000-0001-6250-048X
Sapienza University of Rome · ITUniversity of Milan · ITAzienda Ospedaliera San Giovanni Addolorata · ITAzienda Ospedaliera Sant'Andrea · ITAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITIstituto Euro Mediterraneo di Scienza e Tecnologia · ITNewYork–Presbyterian Hospital · USOspedale San Bortolo · ITTorbat Heydarieh University of Medical Sciences · IRUniversità Campus Bio-Medico · ITUniversity of Palermo · IT

Funding

Sapienza Università di Roma (Sapienza University of Rome) Ateneo 2016
6 · The paper itself

Abstract

Breast implant-associated anaplastic large cell lymphoma is a new provisional entity in the revised World Health Organization classification of lymphoid malignancies, the pathogenesis and cell of origin of which are still unknown. We performed gene expression profiling of microdissected breast implant-associated anaplastic large cell lymphoma samples and compared their transcriptional profiles with those previously obtained from normal T-cells and other peripheral T-cell lymphomas and validated expression of selected markers by immunohistochemistry. Our results indicate that most breast implant-associated anaplastic large cell lymphomas exhibit an activated CD4+ memory T-cell phenotype, which is associated with CD25 and FoxP3 expression. Gene ontology analyses revealed upregulation of genes involved in cell motility programs (e.g., CCR6, MET, HGF, CXCL14) in breast implant-associated anaplastic large cell lymphomas compared to normal CD4+ T-cells and upregulation of genes involved in myeloid cell differentiation (e.g., PPARg, JAK2, SPI-1, GAB2) and viral gene transcription (e.g., RPS10, RPL17, RPS29, RPL18A) compared to other types of peripheral T-cell lymphomas. Gene set enrichment analyses also revealed shared features between the molecular profiles of breast implant-associated anaplastic large cell lymphomas and other types of anaplastic large cell lymphomas, including downregulation of T-cell receptor signaling and STAT3 activation. Our findings provide novel insights into the biology of this rare disease and further evidence that breast implant-associated anaplastic large cell lymphoma represents a distinct peripheral T-cell lymphoma entity.

Indexed as

AdultBreast ImplantsFemaleHumansLymphoma, Large-Cell, AnaplasticLymphoma, T-Cell, PeripheralTranscriptome

Identifiers

PMID30206415
OpenAlexW2891390890

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.