Evidence map›Paper›PMID 22801218›Full record

ArticleBiochimica et biophysica acta2012

Pdcd4 knockdown up-regulates MAP4K1 expression and activation of AP-1 dependent transcription through c-Myc.

Qing Wang, Yan Zhang, Hsin-Sheng Yang

Abstract read
In one paragraph

Article in Biochimica et biophysica acta, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The Impact of Pdcd4, a Translation Inhibitor, on Drug Resistance.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. DTL promotes cancer progression by PDCD4 ubiquitin-dependent degradation.Journal of experimental & clinical cancer research : CR · 2019
    Article
  12. Article
  13. Control Mechanisms of the Tumor Suppressor PDCD4: Expression and Functions.International journal of molecular sciences · 2019
    Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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.

Qing WangGraduate Center for Toxicology, College of Medicine, University of Kentucky, Lexington, KY 40536, USA.
Yan Zhang
Hsin-Sheng Yang
The Graduate Center, CUNY · US

Funding

The role of Pdcd4 in colorectal tumor progressionR01CA129015 · NCI · UNIVERSITY OF KENTUCKY · PI YANG, HSIN-SHENG · 2009 to 2013
$1.5M
NCI NIH HHS R01 CA129015NCI NIH HHS R01CA 129015
6 · The paper itself

Abstract

Programmed cell death 4 (Pdcd4) is a novel tumor suppressor, whose expression is frequently down-regulated in several types of cancers. In the present study, we demonstrated that Pdcd4 knockdown up-regulates MAP kinase kinase kinase kinase 1 (MAP4K1) expression and increases phosphorylation of c-Jun. Over-expression of c-Myc in HEK293 cells increases the levels of MAP4K1, MAP4K1 promoter activity, and phospho-c-Jun. Mutation analysis showed that the c-Myc binding site at -536bp (relative to the initiation ATG) of map4k1 promoter responds to c-Myc regulation. In addition, chromatin immunoprecipitation demonstrated that c-Myc directly binds to map4k1 promoter at this site. Down-regulation of c-Myc reverses MAP4K1 expression and AP-1 activation in Pdcd4 knockdown cells. Moreover, over-expression of dominant negative Tcf4 decreases expression of c-Myc and MAP4K1, JNK activation, and AP-1 dependent transcription. Thus, activation of β-catenin/Tcf dependent transcription in Pdcd4 knockdown cells up-regulates MAP4K1 expression and AP-1 activity via c-Myc. The study presented here further reveals in detail the mechanism of how Pdcd4 inhibits tumor cell invasion and provides a functional connection between β-catenin/Tcf and AP-1 dependent transcription.

Indexed as

Gene Knockdown TechniquesTranscription, GeneticApoptosis Regulatory Proteinsbeta CateninBinding SitesDown-RegulationEnzyme ActivationHEK293 CellsHumansJNK Mitogen-Activated Protein KinasesMAP Kinase Signaling SystemModels, BiologicalPromoter Regions, GeneticProtein Serine-Threonine KinasesProto-Oncogene Proteins c-junProto-Oncogene Proteins c-mycApoptosis Regulatory Proteinsbeta Cateninhematopoietic progenitor kinase 1JNK Mitogen-Activated Protein KinasesPDCD4 protein, humanProtein Serine-Threonine KinasesProto-Oncogene Proteins c-junProto-Oncogene Proteins c-mycRNA-Binding ProteinsTCF Transcription FactorsTranscription Factor AP-1

Identifiers

PMID22801218
PMCPMC3725281
OpenAlexW2090222973

What OpenQuestion holds

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LicenceTDM
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.