Evidence map›Paper›PMID 12913110›Full record

ArticleThe Journal of cell biology2003

FOXO transcription factors directly activate bim gene expression and promote apoptosis in sympathetic neurons.

Jonathan Gilley, Paul J Coffer, Jonathan Ham

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 315 papers.

0numbers the graph read from it
0cells of the map it votes in
315citing papers in PubMed
12.2field-weighted citation impact, top 1% 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

315 citing papers in PubMed, 639 citations in OpenAlex.

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  13. Acetylation of FOXO1 activates Bim expression involved in CVB3 induced cardiomyocyte apoptosis.Apoptosis : an international journal on programmed cell death · 2024
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255 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 2 countries.

Jonathan GilleyMolecular Haematology and Cancer Biology Unit, Camelia Botnar Laboratories, Institute of Child Health, University College London, 30 Guilford St., London WC1N 1EH, UK.
Paul J Coffer
Jonathan Ham
University College London · GBUniversity Medical Center Utrecht · NL

Funding

Wellcome Trust
6 · The paper itself

Abstract

Developing sympathetic neurons die by apoptosis when deprived of NGF. BIM, a BH3-only member of the BCL-2 family, is induced after NGF withdrawal in these cells and contributes to NGF withdrawal-induced death. Here, we have investigated the involvement of the Forkhead box, class O (FOXO) subfamily of Forkhead transcription factors in the regulation of BIM expression by NGF. We find that overexpression of FOXO transcription factors induces BIM expression and promotes death of sympathetic neurons in a BIM-dependent manner. In addition, we find that FKHRL1 (FOXO3a) directly activates the bim promoter via two conserved FOXO binding sites and that mutation of these sites abolishes bim promoter activation after NGF withdrawal. Finally, we show that FOXO activity contributes to the NGF deprivation-induced death of sympathetic neurons.

Indexed as

Membrane ProteinsProto-Oncogene ProteinsAnimalsApoptosisApoptosis Regulatory ProteinsBcl-2-Like Protein 11Binding SitesCarrier ProteinsDNA-Binding ProteinsForkhead Box Protein O1Forkhead Box Protein O3Forkhead Transcription FactorsNerve Growth FactorNerve Tissue ProteinsNeuronsPhosphatidylinositol 3-KinasesApoptosis Regulatory ProteinsBcl2l11 protein, ratBcl-2-Like Protein 11Carrier ProteinsDNA-Binding ProteinsForkhead Box Protein O1Forkhead Box Protein O3Forkhead Transcription FactorsFoxo1 protein, ratFOXO3 protein, ratMembrane ProteinsNerve Growth FactorNerve Tissue ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene ProteinsTranscription Factors

Identifiers

PMID12913110
PMCPMC2173804
OpenAlexW2065678329

What OpenQuestion holds

Textmetadata
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.