Evidence map›Paper›PMID 11988839›Full record

ArticleNeoplasia (New York, N.Y.)

The human p73 promoter: characterization and identification of functional E2F binding sites.

Ratnam S Seelan, Meredith Irwin, Petra van der Stoop, Chiping Qian, William G Kaelin, Wanguo Liu

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-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

22 citing papers in PubMed, 47 citations in OpenAlex.

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  12. p73 in Cancer.Genes & cancer · 2011
    Article
  13. p73 as a pharmaceutical target for cancer therapy.Current pharmaceutical design · 2011
    Review
  14. Article
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  19. Developmental roles of p73 in Cajal-Retzius cells and cortical patterning.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004
    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

6 authors at 3 institutions in 1 country.

Ratnam S SeelanDepartment of Laboratory Medicine and Pathology, Division of Experimental Pathology, Mayo Clinic and Mayo Medical School, 200 First Street SW, Rochester, MN 55905, USA.
Meredith Irwin
Petra van der Stoop
Chiping Qian
William G Kaelin
Wanguo Liu
Mayo Clinic in Arizona · USDana-Farber Brigham Cancer Center · USHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

p73, a member of the p53 family, is overexpressed in many cancers. To understand the mechanism(s) underlying this overexpression, we have undertaken a detailed characterization of the human p73 promoter. The promoter is strongly activated in cells expressing exogenous E2F1 and suppressed by exogenous Rb. At least three functional E2F binding sites, located immediately upstream of exon 1 (at -284, -155 and -132) mediate this induction. 5' serially deleted promoter constructs and constructs harboring mutated E2F sites were analyzed for their response to exogenously expressed E2F1 or Rb to establish functionality of these sites. Authenticity of E2F sites was further confirmed by electrophoretic mobility shift assay (EMSA) using E2F1/DP1 heterodimers synthesized in vitro, followed by competition assays with unlabeled wild-type or mutant oligonucleotides and supershift analysis using anti-E2F1 antibodies. In vivo binding of E2F1 to the p73 promoter was demonstrated using nuclear extracts prepared from E2F1-inducible Saos2 cells. The region conferring the highest promoter activity was found to reside between -113 to -217 of the p73 gene. Two of the three functional E2F sites (at -155 and -132) reside within this region. Our results suggest that regulation of p73 expression is primarily mediated through binding of E2F1 to target sites at -155 and -132.

Indexed as

Cell Cycle ProteinsGene Expression Regulation, NeoplasticPromoter Regions, GeneticBase SequenceBinding SitesDimerizationDNA-Binding ProteinsE2F1 Transcription FactorE2F Transcription FactorsExonsGene DeletionGenes, Tumor SuppressorHeLa CellsHumansModels, GeneticMolecular Sequence DataCell Cycle ProteinsDNA-Binding ProteinsE2F1 protein, humanE2F1 Transcription FactorE2F Transcription FactorsNuclear ProteinsTP73 protein, humanTranscription FactorsTumor Protein p73Tumor Suppressor Proteins

Identifiers

PMID11988839
PMCPMC1531693
OpenAlexW2094810871

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.