Evidence map›Paper›PMID 40064891›Full record

ArticleNature communications2025

Suppression of stress granule formation is a vulnerability imposed by mutant p53.

Elizabeth Thoenen, Atul Ranjan, Alejandro Parrales, Shigeto Nishikawa, Dan A Dixon, Sugako Oka, Tomoo Iwakuma

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Emerging roles of stress granules in liver diseases: a comprehensive review.Frontiers in cell and developmental biology · 2025
    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

7 authors.

Elizabeth ThoenenDepartment of Pediatrics, Division of Hematology & Oncology, Children's Mercy Research Institute, Kansas City, MO, USA.ORCID http://orcid.org/0000-0002-2603-8459
Atul RanjanDepartment of Pediatrics, Division of Hematology & Oncology, Children's Mercy Research Institute, Kansas City, MO, USA.
Alejandro ParralesDepartment of Pediatrics, Division of Hematology & Oncology, Children's Mercy Research Institute, Kansas City, MO, USA.
Shigeto NishikawaDepartment of Pediatrics, Division of Hematology & Oncology, Children's Mercy Research Institute, Kansas City, MO, USA.
Dan A DixonDepartment of Biochemistry and Molecular Biology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Sugako OkaFaculty of Medical Science, Kyushu University, Fukuoka, Japan.
Tomoo IwakumaDepartment of Pediatrics, Division of Hematology & Oncology, Children's Mercy Research Institute, Kansas City, MO, USA. tiwakuma@cmh.edu.ORCID http://orcid.org/0000-0001-7249-7958

Funding

Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI NICOLE L NOLLEN · 2012 to 2026
$40.1M
Control of mutant p53 stability via the mevalonate pathway-DNAJA1 axisR01CA214916 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI IWAKUMA, TOMOO · 2018 to 2022
$1.8M
Simultaneous ROS production and DDR inhibition to trigger p53 synthetic lethalityR01CA285616 · NCI · CHILDREN'S MERCY HOSP (KANSAS CITY, MO) · PI Tomoo Iwakuma · 2025 to 2026
$1.1M
NCI NIH HHS P30 CA168524NCI NIH HHS R01 CA214916NCI NIH HHS R01 CA285616
6 · The paper itself

Abstract

Missense mutations in the TP53 (p53) gene have been linked to malignant progression. However, our in-silico analyses reveal that hepatocellular carcinoma (HCC) patients with mutant p53 (mutp53) have better overall survival compared to those with p53-null (p53

Indexed as

Carcinoma, HepatocellularEndoplasmic Reticulum StressLiver NeoplasmsStress GranulesTumor Suppressor Protein p53AnimalsCell Line, TumorDNA HelicaseseIF-2 KinaseFemaleHumansMiceMutationPoly-ADP-Ribose Binding ProteinsRNA HelicasesRNA Recognition Motif ProteinsDNA HelicaseseIF-2 KinaseG3BP1 protein, humanPoly-ADP-Ribose Binding ProteinsRNA HelicasesRNA Recognition Motif ProteinsSorafenibTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID40064891
PMCPMC11894096

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.