Evidence map›Paper›PMID 24488925›Full record

ReviewHuman mutation2014

The Mdm network and its regulation of p53 activities: a rheostat of cancer risk.

Christine M Eischen, Guillermina Lozano

Abstract readReview
In one paragraph

Review in Human mutation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 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.

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

50 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Clausenidin from Clausena excavata Burm. causes Apoptosis of Liver Cancer in Mice.Asian Pacific journal of cancer prevention : APJCP · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Association of MDM2 Overexpression in Ameloblastomas withInternational journal of molecular sciences · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. The roles of E3 ligases in Hepatocellular carcinoma.American journal of cancer research · 2022
    Review
  16. Article
  17. Article
  18. Role of mismatch repair in aging.International journal of biological sciences · 2021
    Review
  19. Mdm2: Open questions.Cancer science · 2020
    Review
  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

2 authors.

Christine M EischenVanderbilt University Medical Center, Department of Pathology, Microbiology and Immunology, Nashville, Tennessee.
Guillermina Lozano

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
PATHWAY OF TUMOR SUPPRESSIONR01CA047296 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GUILLERMINA LOZANO · 1993 to 2026
$8.0M
SMARCAL1 function in replication stress and diseaseR01CA160432 · NCI · VANDERBILT UNIVERSITY · PI CORTEZ, DAVID K, EISCHEN, CHRISTINE M. · 2012 to 2016
$2.3M
p53-Independent Pathways in Mdm2-Mediated TransformationR01CA117935 · NCI · VANDERBILT UNIVERSITY · PI EISCHEN, CHRISTINE M. · 2007 to 2011
$1.5M
NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA068485NCI NIH HHS R01 CA047296NCI NIH HHS R01 CA117935NCI NIH HHS R01 CA160432
6 · The paper itself

Abstract

The potent transcriptional activity of p53 (Trp53, TP53) must be kept in check for normal cell growth and survival. Tumors, which drastically deviate from these parameters, have evolved multiple mechanisms to inactivate TP53, the most prevalent of which is the emergence of TP53 missense mutations, some of which have gain-of-function activities. Another important mechanism by which tumors bypass TP53 functions is via increased levels of two TP53 inhibitors, MDM2, and MDM4. Studies in humans and in mice reveal the complexity of TP53 regulation and the exquisite sensitivity of this pathway to small changes in regulation. Here, we summarize the factors that impinge on TP53 activity and thus cell death/arrest or tumor development.

Indexed as

AnimalsCell Cycle CheckpointsCell Cycle ProteinsCell DeathCell ProliferationHumansMiceNeoplasmsNuclear ProteinsProto-Oncogene ProteinsProto-Oncogene Proteins c-mdm2Risk FactorsTranscription, GeneticTumor Suppressor Protein p53Cell Cycle ProteinsMDM2 protein, humanMDM4 protein, humanNuclear ProteinsProto-Oncogene ProteinsProto-Oncogene Proteins c-mdm2TP53 protein, humanTumor Suppressor Protein p53Mdm2Mdm4mouse modelsp53TCGATP53Trp53

Identifiers

PMID24488925
PMCPMC4725600

What OpenQuestion holds

Textmetadata
LicenceTDM
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.