Evidence map›Paper›PMID 21391906›Full record

ReviewCurrent pharmaceutical design2011

Pharmacologic activation of p53 by small-molecule MDM2 antagonists.

Hong Shen, Carl G Maki

Open access · greenAbstract readReview
In one paragraph

Review in Current pharmaceutical design, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
3.1field-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

81 citing papers in PubMed, 151 citations in OpenAlex.

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  15. TP53 mutations and MDM2 polymorphisms in breast and ovarian cancers: amelioration by drugs and natural compounds.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  16. Article
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21 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 at 1 institution in 1 country.

Hong ShenDepartment of Anatomy and Cell Biology Rush University Medical Center 1750 W Harrison Ave Jelke Building, Room 1306, USA.
Carl G Maki
Rush University Medical Center · US

Funding

Cellular Responses to p53 Activation by Nutlin-3aR01CA137598 · NCI · RUSH UNIVERSITY MEDICAL CENTER · PI MAKI, CARL G · 2009 to 2013
$1.5M
NCI NIH HHS 1R01CA137598-01A1NCI NIH HHS R01 CA137598
6 · The paper itself

Abstract

Restoring p53 activity by inhibiting the interaction between p53 and MDM2 represents an attractive approach for cancer therapy. To this end, a number of small-molecule p53-MDM2 binding inhibitors have been developed during the past several years. Nutlin-3 is a potent and selective small-molecule MDM2 antagonist that has shown considerable promise in pre-clinical studies. This review will highlight recent advances in the development of small-molecule MDM2 antagonists as potential cancer therapeutics, with special emphasis on Nutlin-3.

Indexed as

Genes, p53Antineoplastic AgentsHumansImidazolesMolecular Targeted TherapyNeoplasmsPiperazinesProtein BindingProto-Oncogene Proteins c-mdm2Tumor Suppressor Protein p53Antineoplastic AgentsImidazolesMDM2 protein, humannutlin 3PiperazinesProto-Oncogene Proteins c-mdm2Tumor Suppressor Protein p53

Identifiers

PMID21391906
PMCPMC3613239
OpenAlexW2030738890

What Socratic 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 Socratic graph.