Evidence map›Paper›PMID 8552074›Full record

ArticleMolecular and cellular biology1996

Transcriptional down regulation of the nov proto-oncogene in fibroblasts transformed by p60v-src.

G Scholz, C Martinerie, B Perbal, H Hanafusa

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

26 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. CCN proteins: A centralized communication network.Journal of cell communication and signaling · 2013
    Article
  5. Article
  6. Article
  7. Article
  8. NOV story: the way to CCN3.Cell communication and signaling : CCS · 2006
    Article
  9. Article
  10. Potential cellular conformations of the CCN3(NOV) protein.Cell communication and signaling : CCS · 2004
    Article
  11. The expression of ccn3(nov) gene in musculoskeletal tumors.The American journal of pathology · 2002
    Article
  12. Article
  13. Article
  14. Article
  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

4 authors at 3 institutions in 2 countries.

G ScholzLaboratory of Molecular Oncology, Rockefeller University, New York, New York 10021, USA.
C Martinerie
B Perbal
H Hanafusa
Rockefeller University · USDélégation Paris 7 · FRLaboratoire de Virologie Moléculaire et Structurale · FR

Funding

CELL TRANSFORMATION BY RETROVIRUSR35CA044356 · NCI · ROCKEFELLER UNIVERSITY · PI HANAFUSA, HIDESABURO · 1987 to 1999
–
NCI NIH HHS CA44356
6 · The paper itself

Abstract

We have sought to identify genes whose expression is altered as a consequence of transformation by p60v-src. Using the mRNA differential display method, we have identified the nov proto-oncogene as one gene that is down regulated in chicken embryo fibroblasts (CEFs) transformed by p60v-src. nov transcripts were also found to be present at only very low levels in proliferating CEFs in comparison with quiescent CEFs. Serum stimulation of quiescent CEFs also resulted in a decline in the steady-state level of nov transcripts. Taken together, these findings suggest that the nov gene is expressed only in quiescent fibroblasts and that its down regulation may contribute to cellular transformation by the v-src oncogene. Down regulation of the nov gene appears to occur at both the transcriptional and posttranscriptional levels. Results obtained from experiments with a protein kinase inhibitor suggest that protein kinase C may be a key downstream effector in mediating the down regulation of nov transcripts in response to activation of p60src or serum stimulation. In addition, we found that transcription of an unknown gene is required for the decline in the steady-state level of nov transcripts in response to serum stimulation.

Indexed as

Gene Expression Regulation, NeoplasticImmediate-Early ProteinsIntercellular Signaling Peptides and ProteinsTranscription, Genetic1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineAnimalsCell DivisionCell NucleusCells, CulturedCell Transformation, NeoplasticChickensConnective Tissue Growth FactorDown-RegulationEnzyme InhibitorsFibroblastsIsoquinolines1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineConnective Tissue Growth FactorEnzyme InhibitorsImmediate-Early ProteinsIntercellular Signaling Peptides and ProteinsIsoquinolinesOncogene Protein pp60(v-src)Oncogene ProteinsOncogene Proteins, ViralPiperazinesProtein Kinase CProto-Oncogene ProteinsRNA, Messenger

Identifiers

PMID8552074
PMCPMC231025
OpenAlexW2138962762

What Socratic 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 Socratic graph.