Evidence map›Paper›PMID 39587609›Full record

ArticleJournal of experimental & clinical cancer research : CR2024

Selective metabolic regulations by p53 mutant variants in pancreatic cancer.

Sabrina Caporali, Alessio Butera, Alessia Ruzza, Carlotta Zampieri, Marina Bantula', Sandra Scharsich, Anna-Katerina Ückert, Ivana Celardo, Ian U Kouzel, Luigi Leanza and 6 more

Abstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
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

16 authors.

Sabrina Caporali *Chair for Systems Toxicology, Department of Biology, University of Konstanz, Konstanz, Germany.
Alessio Butera *Chair for Systems Toxicology, Department of Biology, University of Konstanz, Konstanz, Germany.
Alessia Ruzza *Chair for Systems Toxicology, Department of Biology, University of Konstanz, Konstanz, Germany.
Carlotta ZampieriDepartment of Pathology, University of California San Diego School of Medicine, La Jolla, San Diego, CA, USA.
Marina Bantula'Department of Biomedical Sciences, Universitat de Barcelona, Casanova 143, Barcelona, 08036, Spain.
Sandra ScharsichChair for Systems Toxicology, Department of Biology, University of Konstanz, Konstanz, Germany.
Anna-Katerina ÜckertChair for in Vitro Toxicology and Biomedicine, University of Konstanz, Constance, Germany.
Ivana CelardoChair for in Vitro Toxicology and Biomedicine, University of Konstanz, Constance, Germany.
Ian U KouzelApplied Bioinformatic Group, University of Konstanz, Constance, Germany.
Luigi LeanzaDepartment of Biology, University of Padua, Padua, Italy.
Andreas GruberApplied Bioinformatic Group, University of Konstanz, Constance, Germany.
Joan MonteroDepartment of Biomedical Sciences, Universitat de Barcelona, Casanova 143, Barcelona, 08036, Spain.
Angelo D'AlessandroUniversity of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA.
Thomas BrunnerChair for in Biochemical Pharmacology, University of Konstanz, Constance, Germany.
Marcel LeistChair for in Vitro Toxicology and Biomedicine, University of Konstanz, Constance, Germany.
Ivano AmelioChair for Systems Toxicology, Department of Biology, University of Konstanz, Konstanz, Germany. ivano.amelio@uni-konstanz.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundApproximately half of all human cancers harbour mutations in the p53 gene, leading to the generation of neomorphic p53 mutant proteins. These mutants can exert gain-of-function (GOF) effects, potentially promoting tumour progression. However, the clinical significance of p53 GOF mutations, as well as the selectivity of individual variants, remains controversial and unclear.

methodsTo elucidate the metabolic regulations and molecular underpinnings associated with the specific p53

resultsOur investigation revealed that the p53

conclusionsOur study elucidates the mutant-specific impact of p53

Indexed as

MutationPancreatic NeoplasmsTumor Suppressor Protein p53AnimalsCell Line, TumorCell ProliferationHumansMiceTP53 protein, humanTumor Suppressor Protein p53Anti-oxidant capacityCancer MetabolismGain-of-functionTumour suppressor

Identifiers

PMID39587609
PMCPMC11590503

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.