Evidence map›Paper›PMID 31719683›Full record

ArticleLeukemia2020

Physiological levels of the PTEN-PI3K-AKT axis activity are required for maintenance of Burkitt lymphoma.

Franziska Gehringer, Stephanie Ellen Weissinger, Peter Möller, Thomas Wirth, Alexey Ushmorov

Open access · hybridAbstract read
In one paragraph

Article in Leukemia, 2020. 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
3.5field-weighted citation impact, top 7% 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, 41 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Franziska GehringerInstitute of Physiological Chemistry, University of Ulm, Ulm, Germany.
Stephanie Ellen WeissingerInstitute of Pathology, University of Ulm, Ulm, Germany.
Peter MöllerInstitute of Pathology, University of Ulm, Ulm, Germany.
Thomas Wirth *Institute of Physiological Chemistry, University of Ulm, Ulm, Germany. thomas.wirth@uni-ulm.de.
Alexey Ushmorov *Institute of Physiological Chemistry, University of Ulm, Ulm, Germany. alexey.ushmorov@uni-ulm.de.ORCID http://orcid.org/0000-0003-3724-7253
Universität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In addition to oncogenic MYC translocations, Burkitt lymphoma (BL) depends on the germinal centre (GC) dark zone (DZ) B cell survival and proliferation programme, which is characterized by relatively low PI3K-AKT activity. Paradoxically, PI3K-AKT activation facilitates MYC-driven lymphomagenesis in mice, and it has been proposed that PI3K-AKT activation is essential for BL. Here we show that the PI3K-AKT activity in primary BLs and BL cell lines does not exceed that of human non-neoplastic tonsillar GC DZ B cells. BLs were not sensitive to AKT1 knockdown, which induced massive cell death in pAKT

Indexed as

ApoptosisB-LymphocytesBurkitt LymphomaCell Line, TumorCell ProliferationCell SurvivalHumansPalatine TonsilPhenotypePhosphatidylinositol 3-KinasesProto-Oncogene MasProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseSignal TransductionMAS1 protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene MasProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, human

Identifiers

PMID31719683
PMCPMC7214272
OpenAlexW2986129865

What OpenQuestion holds

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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.