Evidence map›Paper›PMID 39770524›Full record

ReviewPharmaceuticals (Basel, Switzerland)2024

p53: The Multifaceted Roles of Covalent Modifications in Cancer.

Tatiana A Grigoreva, Angelina A Romanova, Vyacheslav G Tribulovich, Nikolay B Pestov, Ruslan A Oganov, Diana K Kovaleva, Tatyana V Korneenko, Nickolai A Barlev

Abstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. The Dynamic Alliance of p53 and Metabolism in the Tumor Microenvironment Shapes Tumor Evolution.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  2. Nitration in cancer signaling.Redox biology · 2026
    Review
  3. Review
  4. Review
  5. Ambiguous Role of p53 in Transcription-Dependent Tumor Cell Death.International journal of molecular sciences · 2026
    Review
  6. Review
  7. 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

8 authors.

Tatiana A GrigorevaSt. Petersburg State Institute of Technology, St-Petersburg 190013, Russia.
Angelina A RomanovaSt. Petersburg State Institute of Technology, St-Petersburg 190013, Russia.
Vyacheslav G TribulovichSt. Petersburg State Institute of Technology, St-Petersburg 190013, Russia.
Nikolay B PestovInstitute of Biomedical Chemistry, Moscow 119121, Russia.
Ruslan A OganovShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Moscow 117997, Russia.
Diana K KovalevaShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Moscow 117997, Russia.ORCID 0009-0007-6654-1087
Tatyana V KorneenkoShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Moscow 117997, Russia.
Nickolai A BarlevInstitute of Biomedical Chemistry, Moscow 119121, Russia.ORCID 0000-0001-7111-2446

Funding

Ministry of Science and Higher Education of the Russian Federa-tion within the framework of state support for the creation and development of World-Class Research Centers "Digital Bi-odesign and Personalized Healthcare" 75-15-2020-913
6 · The paper itself

Abstract

The p53 protein has attracted huge research interest over several decades due to its role as one of the most important tumor suppressors in mammals, which orchestrates a synchronous response from normal cells in the body to various forms of stress. The diverse cellular activities of the p53 protein are regulated mainly via its post-translational modifications (PTMs). PTMs affect p53 on several levels: at the level of the assembly of tetrameric complexes on DNA to transactivate its target genes, at the level of the assembly of tetrameric complexes on DNA to transactivate its target genes; at the level of proteolysis in the absence of stress; and on the contrary, at the level of augmented protein stability in response to stress signals. Disruptions in these regulatory mechanisms can lead to deviations from normal cellular function, boosting tumor initiation and progression. Conversely, targeted interventions in these pathways could prove beneficial for the development of antitumor therapies. Advancing our understanding of p53 modifiers and the proteins involved in its regulation equips researchers with an expanded toolkit for studying cellular processes and for developing biologically active molecules that influence p53-mediated responses.

Indexed as

E3 ubiquitin ligasesp53posttranslational modifications

Identifiers

PMID39770524
PMCPMC11677429

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.