Evidence map›Paper›PMID 29721381›Full record

ArticleOncoimmunology

FOXO1 promotes resistance of non-Hodgkin lymphomas to anti-CD20-based therapy.

Beata Pyrzynska, Michal Dwojak, Abdessamad Zerrouqi, Giulia Morlino, Piotr Zapala, Nina Miazek, Agnieszka Zagozdzon, Kamil Bojarczuk, Malgorzata Bobrowicz, Marta Siernicka and 9 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

25 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  6. Article
  7. The origin of human CD20Frontiers in immunology · 2024
    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

19 authors at 5 institutions in 3 countries.

Beata PyrzynskaDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Michal DwojakDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Abdessamad ZerrouqiDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Giulia MorlinoThe Francis Crick Institute, London, United Kingdom.
Piotr ZapalaDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Nina MiazekDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Agnieszka ZagozdzonDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Kamil BojarczukDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Malgorzata BobrowiczDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Marta SiernickaDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Marcin M MachnickiDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Stefania GobessiDepartment of Molecular Hematology, International Centre for Genetic Engineering and Biotechnology, Trieste, Italy.
Joanna BarankiewiczDepartment of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
Ewa Lech-MarandaDepartment of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
Dimitar G EfremovDepartment of Molecular Hematology, International Centre for Genetic Engineering and Biotechnology, Trieste, Italy.
Przemyslaw JuszczynskiDepartment of Hematology, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
Dinis CaladoThe Francis Crick Institute, London, United Kingdom.
Jakub GolabDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Magdalena WiniarskaDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Medical University of Warsaw · PLInstytut Hematologii i Transfuzjologi · PLInternational Centre for Genetic Engineering and Biotechnology · ITKing's College London · GBThe Francis Crick Institute · GB

Funding

Cancer Research UK 16857Medical Research Council MR/J008060/1
6 · The paper itself

Abstract

Diminished overall survival rate of non-Hodgkin lymphoma (NHL) patients treated with a combination regimen of rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone (R-CHOP) has been recently linked to recurrent somatic mutations activating FOXO1. Despite of the clinical relevance of this finding, the molecular mechanism driving resistance to R-CHOP therapy remains largely unknown. Herein, we investigated the potential role of FOXO1 in the therapeutic efficacy of rituximab, the only targeted therapy included in the R-CHOP regimen. We found CD20 transcription is negatively regulated by FOXO1 in NHL cell lines and in human lymphoma specimens carrying activating mutations of

Indexed as

CD20FOXO1lymphomaR-CHOPrituximab

Identifiers

PMID29721381
PMCPMC5927521
OpenAlexW2759061414

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.