Evidence map›Paper›PMID 20802531›Full record

ArticleOncogene2010

Suppression of cell-cycle progression by Jun dimerization protein-2 (JDP2) involves downregulation of cyclin-A2.

J Pan, K Nakade, Y-C Huang, Z-W Zhu, S Masuzaki, H Hasegawa, T Murata, A Yoshiki, N Yamaguchi, C-H Lee and 4 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Oncogene, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

37 citing papers in PubMed, 54 citations in OpenAlex.

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  14. Prevention of tumor risk associated with the reprogramming of human pluripotent stem cells.Journal of experimental & clinical cancer research : CR · 2020
    Review
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  16. Article
  17. Article
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  19. Article
  20. Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

14 authors at 6 institutions in 3 countries.

J PanRIKEN BioResource Center, Ibaraki, Japan.
K Nakade
Y-C Huang
Z-W Zhu
S Masuzaki
H Hasegawa
T Murata
A Yoshiki
N Yamaguchi
C-H Lee
W-C Yang
E-M Tsai
Y Obata
K K Yokoyama
RIKEN BioResource Research Center · JPKaohsiung Medical University · TWChiba University · JPAgricultural Biotechnology Research Center, Academia Sinica · TWAnimal Science Research Institute · CNKaohsiung Municipal Hsiao-Kang Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report here a novel role for Jun dimerization protein-2 (JDP2) as a regulator of the progression of normal cells through the cell cycle. To determine the role of JDP2 in vivo, we generated Jdp2-knockout (Jdp2KO) mice by targeting exon-1 to disrupt the site of initiation of transcription. The epidermal thickening of skin from the Jdp2KO mice after treatment with 12-O-tetradecanoylphorbol 13-acetate (TPA) proceeded more rapidly than that of control mice, and more proliferating cells were found at the epidermis. Fibroblasts derived from embryos of Jdp2KO mice proliferated faster and formed more colonies than fibroblasts from wild-type mice. JDP2 was recruited to the promoter of the gene for cyclin-A2 (ccna2) at the AP-1 site. Cells lacking Jdp2 had elevated levels of cyclin-A2 mRNA. Furthermore, reintroduction of JDP2 resulted in the repression of transcription of ccna2 and of cell-cycle progression. Thus, transcription of the gene for cyclin-A2 appears to be a direct target of JDP2 in the suppression of cell proliferation.

Indexed as

Down-RegulationAnimalsApoptosisCell CycleCell LineCell ProliferationCyclin A2Cyclin-Dependent KinasesCyclinsEpidermisGene Knockout TechniquesGenes, ReporterMicePromoter Regions, GeneticRepressor ProteinsCyclin A2Cyclin-Dependent KinasesCyclinsJundp2 protein, mouseRepressor Proteins

Identifiers

PMID20802531
PMCPMC3007677
OpenAlexW2039885364

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.