Evidence map›Paper›PMID 11415456›Full record

ArticleThe Biochemical journal2001

Transforming growth factor beta-1 enhances Smad transcriptional activity through activation of p8 gene expression.

A C García-Montero, S Vasseur, L E Giono, E Canepa, S Moreno, J C Dagorn, J L Iovanna

Abstract read
In one paragraph

Article in The Biochemical journal, 2001. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
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  11. Review
  12. Article
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  14. Article
  15. Recent insights into the cellular mechanisms of acute pancreatitis.Canadian journal of gastroenterology = Journal canadien de gastroenterologie · 2007
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Expression of the stress-associated protein p8 is a requisite for tumor development.International journal of gastrointestinal cancer · 2002
    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

7 authors.

A C García-MonteroINSERM U.315, 46 boulevard de la Gaye, F-13009 Marseille, France.
S Vasseur
L E Giono
E Canepa
S Moreno
J C Dagorn
J L Iovanna

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report that exposure of mouse embryonic fibroblasts to transforming growth factor beta-1 (TGFbeta-1) (5 ng/ml) results in a strong activation of p8 mRNA expression that precedes the induction of cell growth. Involvement of the p8 promoter in the regulation was demonstrated by using a p8-chloramphenicol acetyltransferase construct. We therefore speculated that p8 might be a mediator of TGFbeta-1 in these cells. The incorporation of [(3)H]thymidine on treatment with TGFbeta-1 was indeed significantly higher in p8(+/+) fibroblasts than in p8(-/-) fibroblasts. Smad transcriptional activity was used as marker of the TGFbeta-1 signalling pathway, to probe the lower p8(-/-) response to TGFbeta-1. Two Smad-binding elements (SBEs)-luciferase constructs were transfected into p8(-/-) and p8(+/+) embryonic fibroblasts before treatment with TGFbeta-1. A lower level of Smad transactivation was observed in p8(-/-) embryonic fibroblasts, under basal conditions and after stimulation with TGFbeta-1. To test whether Smad underexpression in p8(-/-) cells was actually due to p8 depletion, p8(-/-) embryonic fibroblasts were transfected with a human p8 expression plasmid together with an SBE-luciferase construct. The expression of p8 restored Smad transactivation in unstimulated and TGFbeta-1-treated cells to the level found in p8(+/+) cells. We concluded that TGFbeta-1 activates p8 expression, which in turn enhances the Smad-transactivating function responsible for TGFbeta-1 activity.

Indexed as

Neoplasm Proteins3T3 CellsAnimalsBasic Helix-Loop-Helix ProteinsCells, CulturedChloramphenicol O-AcetyltransferaseDNADNA-Binding ProteinsEmbryo, MammalianFibroblastsGene DeletionGene Expression RegulationGenes, ReporterGrowth SubstancesHigh Mobility Group ProteinsHomozygoteBasic Helix-Loop-Helix ProteinsChloramphenicol O-AcetyltransferaseDNADNA-Binding ProteinsGrowth SubstancesHigh Mobility Group ProteinsLuciferasesNeoplasm ProteinsNUPR1 protein, humanNupr1 protein, mouseRecombinant Fusion ProteinsRNA, MessengerThymidineTrans-ActivatorsTransforming Growth Factor beta

Identifiers

PMID11415456
PMCPMC1221948

What OpenQuestion holds

Textmetadata
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.