Evidence map›Paper›PMID 22713868›Full record

ReviewGenes & development2012

Mutant p53: one name, many proteins.

William A Freed-Pastor, Carol Prives

Registry-linked trialAbstract readReview
In one paragraph

Review in Genes & development, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02433626 (A Phase 1 Study of COTI-2 as Monotherapy or Combination Therapy for the Treatment of Advanced or Recurrent Malignancies), which is not on this map. Cited by 787 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
787citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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.

NCT02433626 phase1unknown statusnot on this mapstarted 2015, after this paper: background citation

A Phase 1 Study of COTI-2 as Monotherapy or Combination Therapy for the Treatment of Advanced or Recurrent Malignancies

TypeinterventionalSponsorCritical Outcome Technologies Inc.Ran2015 to 2020Enrolled51ConditionsOvarian Cancer, Fallopian Tube Cancer, Endometrial Cancer, Cervical CancerArmsCOTI2, Cisplatin
3 · Its place in the literature

Who cites it

787 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Impact of TP53 somatic mutations on prognosis in endometrial cancer: a systematic review and meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Pooled it
  2. Targeting p53 pathways: mechanisms, structures, and advances in therapy.Signal transduction and targeted therapy · 2023
    Pooled it
  3. Pooled it
  4. Review
  5. Article
  6. Mutant p53Molecular oncology · 2026
    Article
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727 more citing papers are in PubMed but not listed here.

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

2 authors.

William A Freed-PastorDepartment of Biological Sciences, Columbia University, New York, New York 10027, USA.
Carol Prives

Funding

Scientific ReagentsP01CA087497 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI PRIVES, CAROL · 2000 to 2021
$35.4M
PROPERTIES AND REGULATION OF P53 IN TUMOR CELLSR01CA077742 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI PRIVES, CAROL · 1999 to 2014
$3.8M
NCI NIH HHS CA77742NCI NIH HHS CA87497NCI NIH HHS P01 CA087497NCI NIH HHS R01 CA077742
6 · The paper itself

Abstract

There is now strong evidence that mutation not only abrogates p53 tumor-suppressive functions, but in some instances can also endow mutant proteins with novel activities. Such neomorphic p53 proteins are capable of dramatically altering tumor cell behavior, primarily through their interactions with other cellular proteins and regulation of cancer cell transcriptional programs. Different missense mutations in p53 may confer unique activities and thereby offer insight into the mutagenic events that drive tumor progression. Here we review mechanisms by which mutant p53 exerts its cellular effects, with a particular focus on the burgeoning mutant p53 transcriptome, and discuss the biological and clinical consequences of mutant p53 gain of function.

Indexed as

HumansModels, BiologicalMutant ProteinsNeoplasmsProto-Oncogene ProteinsTranscription, GeneticTumor Suppressor Protein p53Mutant ProteinsProto-Oncogene ProteinsTumor Suppressor Protein p53

Identifiers

PMID22713868
PMCPMC3387655

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.