Evidence map›Paper›PMID 15208653›Full record

ArticleOncogene2004

Evidence for a cancer-specific switch at the CDK4 promoter with loss of control by both USF and c-Myc.

Snehalata A Pawar, Marilyn N Szentirmay, Heiko Hermeking, Michèle Sawadogo

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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 2 institutions in 2 countries.

Snehalata A PawarDepartment of Molecular Genetics, The University of Texas, MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA.
Marilyn N Szentirmay
Heiko Hermeking
Michèle Sawadogo
The University of Texas MD Anderson Cancer Center · USMax Planck Institute of Biochemistry · DE

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
MOUSE MODELS FOR USF FUNCTIONR01CA079578 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI SAWADOGO, MICHELE · 1998 to 2002
$454k
NCI NIH HHS CA16672NCI NIH HHS CA79578
6 · The paper itself

Abstract

USF and c-Myc are basic helix-loop-helix transcription factors with similar DNA-binding specificities, but antagonistic effects on cellular transformation. In order to determine how these opposite functions correlate with the transcriptional activities of the two factors on particular downstream targets, we investigated the roles of USF and c-Myc in expression of CDK4, a known direct target of c-Myc. Overexpression of either c-Myc or USF2, but not USF1, stimulated the expression of CDK4 promoter-driven reporter genes in the non-tumorigenic mammary epithelial MCF-10A cells. Dominant-negative mutants specific to either Myc or USF family proteins inhibited reporter gene activity as well as endogenous CDK4 expression, demonstrating involvement of both USF and Myc in CDK4 transcriptional control. In contrast, in two different breast cancer cell lines where USF is transcriptionally inactive and c-Myc is overexpressed, CDK4 promoter activity was no longer responsive to either transcription factor. Accordingly, chromatin immunoprecipitation revealed significantly lower levels of both USF and c-Myc bound to the endogenous CDK4 promoter in breast cancer cells than in MCF-10A cells, with a concomitant decrease in associated histone H3 acetylation. These results suggest that a major switch in the transcriptional control of CDK4 occurs during breast carcinogenesis, with likely alteration of cell cycle regulation.

Indexed as

Gene Expression Regulation, NeoplasticPromoter Regions, GeneticBase SequenceBinding SitesBreastBreast NeoplasmsCell Line, TumorChromatinCyclin-Dependent Kinase 4Cyclin-Dependent KinasesDNA-Binding ProteinsEpithelial CellsFemaleHumansMolecular Sequence DataProtein Structure, TertiaryCDK4 protein, humanChromatinCyclin-Dependent Kinase 4Cyclin-Dependent KinasesDNA-Binding ProteinsProto-Oncogene ProteinsProto-Oncogene Proteins c-mycRNA, MessengerTranscription FactorsUpstream Stimulatory FactorsUSF1 protein, humanUSF2 protein, human

Identifiers

PMID15208653
OpenAlexW2035485568

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.