Evidence map›Paper›PMID 11313943›Full record

ArticleOncogene2001

Expression of a down-regulated target, SSeCKS, reverses v-Jun-induced transformation of 10T1/2 murine fibroblasts.

S B Cohen, A Waha, I H Gelman, P K Vogt

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Reversion of the Jun-induced oncogenic phenotype by enhanced synthesis of sialosyllactosylceramide (GM3 ganglioside).Proceedings of the National Academy of Sciences of the United States of America · 2004
    Article
  11. Article
  12. Article
  13. Article
  14. Genome-scale functional profiling of the mammalian AP-1 signaling pathway.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Jun, the oncoprotein.Oncogene · 2001
    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

4 authors at 2 institutions in 1 country.

S B CohenGen-Probe Incorporated, 10210 Genetic Center Drive, San Diego, California CA 92121, USA.
A Waha
I H Gelman
P K Vogt
Scripps Research Institute · USIcahn School of Medicine at Mount Sinai · US

Funding

SUPPLEMENT TO INVESTIGATIVE HEMATOLOGYT32DK007022 · NIDDK · SCRIPPS RESEARCH INSTITUTE, THE · PI SOLOMON, DANIEL RENEE · 1986 to 2009
$2.3M
ONCOGENES IN VIRUS AND CELLR35CA042564 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI VOGT, PETER K · 1986 to 1999
–
NCI NIH HHS CA42564NIDDK NIH HHS 5 T23 DK 07022
6 · The paper itself

Abstract

Line 10T1/2 mouse fibroblast overexpressing the v-Jun oncoprotein were morphologically altered, grew into multilayered foci in culture and formed colonies when suspended in agar. The growth rate of the v-Jun-transformed 10T1/2 cells was not changed significantly from that of the untransformed parental cells, but the saturation density of the transformed cultures exceeded that of normal controls by a factor of 2. mRNA extracted from v-Jun-transformed 10T1/2 cells was analysed for differential gene expression with DNA micro-array technology. One of the targets downregulated by v-Jun was identified as SSeCKS (Src-suppressed C kinase substrate). Re-expression of SSeCKS in v-Jun-transformed fibroblasts reversed the transformed phenotype of the cells. Their ability to form foci was reduced to background levels, the number and size of agar colonies was lowered by a factor of 10 and the saturation density was significantly diminished. However, expression of SSeCKS had little effect on the morphology of v-Jun-transformed 10T1/2 cells. These data suggest that the SSeCKS protein has growth-attenuating properties. Down-regulation of SSeCKS may be essential for Jun-induced transformation.

Indexed as

Cell Cycle ProteinsA Kinase Anchor ProteinsAnimalsCell DivisionCells, CulturedCell Transformation, NeoplasticDown-RegulationFibroblastsGene Expression Regulation, NeoplasticMiceMitogensOligonucleotide Array Sequence AnalysisOncogene Protein p65(gag-jun)RetroviridaeTumor Stem Cell AssayAkap12 protein, mouseA Kinase Anchor ProteinsCell Cycle ProteinsMitogensOncogene Protein p65(gag-jun)

Identifiers

PMID11313943
OpenAlexW2334666800

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.