Evidence map›Paper›PMID 29151585›Full record

ArticleLeukemia2018

Defining the molecular basis of oncogenic cooperation between TAL1 expression and Pten deletion in T-ALL using a novel pro-T-cell model system.

S Bornschein, S Demeyer, R Stirparo, O Gielen, C Vicente, E Geerdens, B Ghesquière, S Aerts, J Cools, C E de Bock

Open access · hybridAbstract read
In one paragraph

Article in Leukemia, 2018. 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
4.0field-weighted citation impact, top 6% 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, 30 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

10 authors at 3 institutions in 1 country.

S BornscheinKU Leuven Center for Human Genetics, Leuven, Belgium.
S DemeyerKU Leuven Center for Human Genetics, Leuven, Belgium.
R StirparoKU Leuven Center for Human Genetics, Leuven, Belgium.
O GielenKU Leuven Center for Human Genetics, Leuven, Belgium.
C VicenteKU Leuven Center for Human Genetics, Leuven, Belgium.
E GeerdensKU Leuven Center for Human Genetics, Leuven, Belgium.
B GhesquièreVIB Center for Cancer Biology, Leuven, Belgium.
S AertsKU Leuven Center for Human Genetics, Leuven, Belgium.
J CoolsKU Leuven Center for Human Genetics, Leuven, Belgium.
C E de BockKU Leuven Center for Human Genetics, Leuven, Belgium.
KU Leuven · BEVIB-KU Leuven Center for Cancer Biology · BEVIB-KU Leuven Center for Microbiology · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell acute lymphoblastic leukemia (T-ALL) is caused by the accumulation of multiple mutations combined with the ectopic expression of transcription factors in developing T cells. However, the molecular basis underlying cooperation between transcription factor expression and additional oncogenic mutations in driving T-ALL has been difficult to assess due to limited robust T-cell model systems. Here we utilize a new ex vivo pro-T-cell model to study oncogenic cooperation. Using a systems biological approach we first dissect the pro-T-cell signaling network driven by interleukin-7, stem cell factor and Notch1 and identify key downstream Akt, Stat, E2f and Myc genetic signaling networks. Next, this pro-T-cell system was used to demonstrate that ectopic expression of the TAL1 transcription factor and Pten deletion are bona-fide cooperating events resulting in an increased stem cell signature, upregulation of a specific E2f signaling network and metabolic reprogramming with higher influx of glucose carbons into the tricarboxylic acid cycle. This ex vivo pro-T-cell system thereby provides a powerful new model system to investigate how normal T-cell signaling networks are perturbed and/or hijacked by different oncogenic events found in T-ALL.

Indexed as

AnimalsCarcinogenesisHEK293 CellsHumansMiceMice, Inbred C57BLMice, TransgenicMutationOncogenesPrecursor T-Cell Lymphoblastic Leukemia-LymphomaPTEN PhosphohydrolaseSequence DeletionSignal TransductionStem CellsT-Cell Acute Lymphocytic Leukemia Protein 1T-LymphocytesPTEN PhosphohydrolasePten protein, mouseTal1 protein, mouseT-Cell Acute Lymphocytic Leukemia Protein 1Transcription Factors

Identifiers

PMID29151585
PMCPMC5886055
OpenAlexW2769566164

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.