Evidence map›Paper›PMID 31557894›Full record

ArticleCancers2019

FOXO1 Confers Maintenance of the Dark Zone Proliferation and Survival Program and Can Be Pharmacologically Targeted in Burkitt Lymphoma.

Franziska Gehringer, Stephanie E Weissinger, Lotteke Jym Swier, Peter Möller, Thomas Wirth, Alexey Ushmorov

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  5. Emerging role of MYB transcription factors in cancer drug resistance.Cancer drug resistance (Alhambra, Calif.) · 2024
    Review
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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

6 authors at 2 institutions in 2 countries.

Franziska GehringerInstitute of Physiological Chemistry, University of Ulm, 89081 Ulm, Germany. franziska.gehringer@uni-ulm.de.
Stephanie E WeissingerInstitute of Pathology, University of Ulm, 89081 Ulm, Germany. weissinger.stephanie@googlemail.com.
Lotteke Jym SwierDepartment of Pathology and Medical Biology, University of Groningen, 9747 AG Groningen, The Netherlands. l.j.y.m.swier@umcg.nl.ORCID 0000-0003-3463-8654
Peter MöllerInstitute of Pathology, University of Ulm, 89081 Ulm, Germany. peter.moeller@uniklinik-ulm.de.
Thomas WirthInstitute of Physiological Chemistry, University of Ulm, 89081 Ulm, Germany. thomas.wirth@uni-ulm.de.
Alexey UshmorovInstitute of Physiological Chemistry, University of Ulm, 89081 Ulm, Germany. alexey.ushmorov@uni-ulm.de.ORCID 0000-0003-3724-7253
Universität Ulm · DEUniversity of Groningen · NL

Funding

Deutsche Krebshilfe 110564
6 · The paper itself

Abstract

The FOXO1 transcription factor plays a central role in the proliferation and survival of B cells at several stages of differentiation. B cell malignancies, with exception of classical Hodgkin lymphoma, maintain expression of FOXO1 at levels characteristic for their non-malignant counterparts. Extensive expression profiling had revealed that Burkitt lymphoma (BL) show many characteristics of the dark zone (DZ) germinal center (GC) B cell program. Here we show that FOXO1 knockdown inhibits proliferation of human BL cell lines. The anti-proliferative effect of the FOXO1 knockdown is associated with the repression of the DZ B cell program including expression of MYB, CCND3, RAG2, BACH2, and CXCR4. In addition, the induction of signaling pathways of the light zone (LZ) program like NF-κB and PI3K-AKT was observed. Using a rescue experiment we identified downregulation of the proto-oncogene MYB as a critical factor contributing to the antiproliferative effect of FOXO1 knockdown. In an attempt to estimate the feasibility of pharmacological FOXO1 repression, we found that the small molecular weight FOXO1 inhibitor AS1842856 induces cell death and growth arrest in BL cell lines at low concentrations. Interestingly, we found that overactivation of FOXO1 also induces growth inhibition in BL cell lines, indicating the importance of a tight regulation of FOXO1 activity in BL.

Indexed as

Burkitt lymphomaFOXO1germinal center dark zone B cell proliferation program

Identifiers

PMID31557894
PMCPMC6826697
OpenAlexW2976174516

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.