Evidence map›Paper›PMID 34919788›Full record

ArticleMolecular oncology2022

p53 mutations define the chromatin landscape to confer drug tolerance in pancreatic cancer.

Carlotta Zampieri, Emanuele Panatta, Vincenzo Corbo, Alessandro Mauriello, Gerry Melino, Ivano Amelio

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
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  4. Article
  5. Selective metabolic regulations by p53 mutant variants in pancreatic cancer.Journal of experimental & clinical cancer research : CR · 2024
    Article
  6. Article
  7. Review
  8. Review
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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

6 authors at 2 institutions in 2 countries.

Carlotta ZampieriDepartment of Experimental Medicine, TOR, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0002-2502-3853
Emanuele PanattaDepartment of Experimental Medicine, TOR, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0001-8723-9564
Vincenzo CorboUniversity of Verona, Italy.ORCID 0000-0002-6340-8009
Alessandro MaurielloDepartment of Experimental Medicine, TOR, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0002-7351-5676
Gerry MelinoDepartment of Experimental Medicine, TOR, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0001-9428-5972
Ivano AmelioDepartment of Experimental Medicine, TOR, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0002-9126-5391
University of Rome Tor Vergata · ITUniversity of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Somatic inactivation of p53 (TP53) mainly occurs as missense mutations that lead to the acquisition of neomorphic mutant protein forms. p53 mutants have been postulated to exert gain-of-function (GOF) effects, including promotion of metastasis and drug tolerance, which generally contribute to the acquisition of the lethal phenotype. Here, by integrating a p53

Indexed as

Pancreatic NeoplasmsChromatinDrug ToleranceHumansMutationMutation, MissenseTumor Suppressor Protein p53ChromatinTP53 protein, humanTumor Suppressor Protein p53cancer epigeneticschemoresistancechemosensitivitychromatin modificationsgemcitabineSWI/SNF chromatin remodelling complex

Identifiers

PMID34919788
PMCPMC8936522
OpenAlexW4200498805

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.