Evidence map›Paper›PMID 39009816›Full record

ReviewNature cancer2024

p53 at the crossroads of tumor immunity.

Gizem Efe, Anil K Rustgi, Carol Prives

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Article
  2. TP53 mutation-biased CD8British journal of cancer · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Revisiting tumor immunogenicity through the lens of mutant p53: Implications for cancer immunotherapy.Apoptosis : an international journal on programmed cell death · 2026
    Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Frontiers in immunology · 2026
    Article
  19. Article
  20. 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

3 authors.

Gizem EfeHerbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-1153-3326
Anil K RustgiHerbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, USA. akr2164@cumc.columbia.edu.
Carol PrivesHerbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY, USA. clp3@columbia.edu.ORCID http://orcid.org/0000-0003-1846-5562

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
Transformed Esophageal Epithelial Cells and the Tumor MicroenvironmentP01CA098101 · NCI · UNIVERSITY OF PENNSYLVANIA · PI HIBSHOOSH, HANINA · 2003 to 2023
$31.7M
Functions and Activities of p53 and Mdm2 in Normal and Cancer CellsR35CA220526 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI PRIVES, CAROL · 2018 to 2024
$6.0M
Mechanisms underlying gastric intestinal metaplasia and carcinogenesisR01CA272903 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Joel Gabre, Maria Gonzalez-Pons · 2022 to 2026
$4.7M
Elucidation of mutant p53-medidated mechanisms in promoting metastatic esophageal cancerF31CA275369 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI EFE, GIZEM · 2022 to 2024
$93k
U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) F31CA275369-02U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P01-CA098101U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P30CA013696U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01CA272903-01U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R35CA220526
6 · The paper itself

Abstract

The p53 tumor suppressor protein has a plethora of cell-intrinsic functions and consequences that impact diverse cell types and tissues. Recent studies are beginning to unravel how wild-type and mutant p53 work in distinct ways to modulate tumor immunity. This sets up a disequilibrium between tumor immunosurveillance and escape therefrom. The ability to exploit this emerging knowledge for translational approaches may shape immunotherapy and targeted therapeutics in the future, especially in combinatorial settings.

Indexed as

NeoplasmsTumor Suppressor Protein p53AnimalsHumansImmunotherapyMutationTumor EscapeTP53 protein, humanTumor Suppressor Protein p53

Identifiers

What OpenQuestion holds

Textmetadata
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.