Evidence map›Paper›PMID 23954639›Full record

ReviewCell metabolism2013

Metabolic regulation by p53 family members.

Celia R Berkers, Oliver D K Maddocks, Eric C Cheung, Inbal Mor, Karen H Vousden

Open access · hybridAbstract readReview
In one paragraph

Review in Cell metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 278 papers.

0numbers the graph read from it
0cells of the map it votes in
278citing papers in PubMed
22.9field-weighted citation impact, top 1% 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

278 citing papers in PubMed, 441 citations in OpenAlex.

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  19. Interplay between altered metabolism and DNA damage and repair in ovarian cancer.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Review
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218 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

5 authors at 1 institution in 1 country.

Celia R BerkersThe CR-UK Beatson Institute, Glasgow G61 1BD, Scotland, UK.
Oliver D K Maddocks
Eric C Cheung
Inbal Mor
Karen H Vousden
Cancer Research UK Scotland Institute · GB

Funding

Canadian Institutes of Health ResearchCancer Research UK
6 · The paper itself

Abstract

The function of p53 is best understood in response to genotoxic stress, but increasing evidence suggests that p53 also plays a key role in the regulation of metabolic homeostasis. p53 and its family members directly influence various metabolic pathways, enabling cells to respond to metabolic stress. These functions are likely to be important for restraining the development of cancer but could also have a profound effect on the development of metabolic diseases, including diabetes. A better understanding of the metabolic functions of p53 family members may aid in the identification of therapeutic targets and reveal novel uses for p53-modulating drugs.

Indexed as

Metabolic Networks and PathwaysAgingAnimalsAutophagyDiseaseHumansReactive Oxygen SpeciesTumor Suppressor Protein p53Reactive Oxygen SpeciesTumor Suppressor Protein p53

Identifiers

PMID23954639
PMCPMC3824073
OpenAlexW2154260730

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.