Evidence map›Paper›PMID 19106608›Full record

ReviewCell cycle (Georgetown, Tex.)2009

Transforming growth factor beta (TGFbeta)-induced apoptosis: the rise & fall of Bim.

Sneha Ramesh, Gary M Wildey, Philip H Howe

Open access · bronzeAbstract readReview
In one paragraph

Review in Cell cycle (Georgetown, Tex.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

59 citing papers in PubMed, 95 citations in OpenAlex.

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  15. BannMI deciphers potentialBioinformatics advances · 2024
    Article
  16. Review
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  19. Article
  20. Review
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 1 institution in 1 country.

Sneha RameshDepartment of Cancer Biology, Lerner Research Institute, Cleveland Clinic Foundation, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
Gary M Wildey
Philip H Howe
Cleveland Clinic · US

Funding

TRANSFORMING GROWTH FACTOR BETA SIGNALING PATHWAYSR01CA055536 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI HOWE, PHILIP H · 1997 to 2017
$5.0M
TGF BETA--INDUCED APOPTOSIS IN B LYMPHOCYTESR01CA080095 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI HOWE, PHILIP H · 1999 to 2013
$3.6M
TRAINING PROGRAM IN VASCULAR CELL BIOLOGYT32HL007914 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI PLOW, EDWARD FRANKLIN · 1999 to 2011
$2.2M
CELL CYLCE REGULATION OF EPITHELIAL CELL GROWTHR29CA055536 · NCI · CLEVELAND CLINIC FOUNDATION · PI HOWE, PHILIP H · 1992 to 1996
–
NCI NIH HHS CA 55536NCI NIH HHS CA 80095NCI NIH HHS R01 CA055536NCI NIH HHS R01 CA080095NHLBI NIH HHS T32 HL 007914NHLBI NIH HHS T32 HL007914
6 · The paper itself

Abstract

Transforming growth factor beta (TGFbeta) regulates essential cellular functions such as cellular proliferation, differentiation and apoptosis. Multiple apoptotic mediators and signaling pathways have been implicated in TGFbeta-induced apoptosis. Bim, a BH3-only protein, is critical for apoptosis in a variety of cell types. In resting cells, BimEL expression levels, the major and most abundant isoform, are controlled by Erk1/2-mediated phosphorylation, which targets BimEL for ubiquitination and degradation. We previously reported that TGFbeta induces the expression of the pro-apoptotic protein Bim through a Smad3-dependent mechanism to induce cell death in B-lymphocytes. A number of studies have shown TGFbeta to cause transcriptional induction of Bim in many cell types. Recently, we demonstrated that, in addition to its transcriptional effects on Bim, TGFbeta induces a MAPK phosphatase (MKP), MKP2/DUSP4, to rapidly increase BimEL levels by inactivation of Erk1/2, resulting in dephosphorylation and escape of BimEL from ubiquitin-mediated degradation. Our findings are of importance not only in the context that we implicate TGFbeta to increase BimEL levels through both an immediate post-translational regulatory mechanism and a long-term effect through transcriptional induction, but also in the context of implicating MKPs as regulatory players in apoptosis. Here we summarize these recent findings and their significance to our understanding of how TGFbeta mediates apoptosis, and we explore the possible regulatory mechanisms controlling Bim expression levels.

Indexed as

ApoptosisAnimalsApoptosis Regulatory ProteinsBcl-2-Like Protein 11Dual-Specificity PhosphatasesEnzyme InductionHumansMembrane ProteinsProto-Oncogene ProteinsTranscription, GeneticTransforming Growth Factor betaApoptosis Regulatory ProteinsBCL2L11 protein, humanBcl-2-Like Protein 11Dual-Specificity PhosphatasesMembrane ProteinsProto-Oncogene ProteinsTransforming Growth Factor beta

Identifiers

PMID19106608
PMCPMC3191464
OpenAlexW2023698635

What OpenQuestion holds

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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.