Evidence map›Paper›PMID 15077194›Full record

ArticleOncogene2004

Tumor-derived p53 mutants induce oncogenesis by transactivating growth-promoting genes.

Mariano J Scian, Katherine E R Stagliano, Debabrita Deb, Michelle A Ellis, Evie H Carchman, Anindita Das, Kristopher Valerie, Swati Palit Deb, Sumitra Deb

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 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

59 citing papers in PubMed, 117 citations in OpenAlex.

  1. Article
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  13. Review
  14. Molecular crosstalk between cancer and neurodegenerative diseases.Cellular and molecular life sciences : CMLS · 2020
    Review
  15. Article
  16. Review
  17. Cancer Stemness: p53 at the Wheel.Frontiers in oncology · 2020
    Review
  18. Article
  19. Article
  20. 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

9 authors at 1 institution in 1 country.

Mariano J ScianDepartment of Biochemistry and the Massey Cancer Center, Virginia Commonwealth University, PO Box 980614, Richmond, VA 23298, USA.
Katherine E R Stagliano
Debabrita Deb
Michelle A Ellis
Evie H Carchman
Anindita Das
Kristopher Valerie
Swati Palit Deb
Sumitra Deb
Virginia Commonwealth University · US

Funding

OVEREXPRESSION OF MDM2 IN THE ETIOLOGY OF BREAST CANCERR01CA074172 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI DEB, SWATI P · 1998 to 2001
$448k
BREAST CANCER ETIOLOGY--P53 GAIN OF FUNCTION MUTATIONSR01CA070712 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI DEB, SUMITRA · 1996 to 2000
$223k
Role of Tumor Suppressor p53 in Breast CancerF31CA097520 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI SCIAN, MARIANO J · 2002 to 2004
$87k
NCI NIH HHS 1 F31 CA97520NCI NIH HHS CA70712NCI NIH HHS CA74172
6 · The paper itself

Abstract

We have studied the mechanism of mutant p53-mediated oncogenesis using several tumor-derived mutants. Using a colony formation assay, we found that the majority of the mutants increased the number of colonies formed compared to the vector. Expression of tumor-derived p53 mutants increases the rate of cell growth, suggesting that the p53 mutants have 'gain of function' properties. We have studied the gene expression profile of cells expressing tumor-derived p53-D281G to identify genes transactivated by mutant p53. We report the transactivation of two genes, asparagine synthetase and human telomerase reverse transcriptase. Quantitative real-time PCR confirms this upregulation. Transient transfection promoter assays verify that tumor-derived p53 mutants transactivate these promoters significantly. An electrophoretic mobility shift assay shows that tumor-derived p53-mutants cannot bind to the wild-type p53 consensus sequence. The results presented here provide some evidence of a possible mechanism for mutant p53-mediated transactivation.

Indexed as

Genes, p53Amino Acid SubstitutionAspartate-Ammonia LigaseCell DivisionCell Line, TumorCell Transformation, NeoplasticConsensus SequenceDNA-Binding ProteinsGene Expression ProfilingGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHumansMutation, MissenseNeoplasmsNuclear ProteinsPoint MutationAspartate-Ammonia LigaseDNA-Binding ProteinsNuclear ProteinsRecombinant Fusion ProteinsTelomeraseTumor Protein p73Tumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID15077194
OpenAlexW2028640227

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.