Evidence map›Paper›PMID 41246646›Full record

ArticleCureus2025

TP53 P72R Polymorphism Is Associated With P53 Protein Expression in Fatal Prostate Cancer: A Novel Case Report and Review of the Literature.

Pooria Asili, Jordan Selep, Coen J Lap, Maneesh Jain, Victor E Nava

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Pooria AsiliDepartment of Pathology and Laboratory Medical Service, Veterans Affairs Medical Center, Washington, DC, USA.
Jordan SelepDepartment of Hematology and Oncology, Veterans Affairs Medical Center, Washington, DC, USA.
Coen J LapDepartment of Hematology and Oncology, Veterans Health Administration, Washington, DC, USA.
Maneesh JainDepartment of Hematology and Oncology, Veterans Affairs Medical Center, Washington, DC, USA.
Victor E NavaDepartment of Pathology and Laboratory Medical Service, Veterans Health Administration, Washington, DC, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Somatic alterations of TP53 in prostate cancer (PCa) are linked to high-grade tumors, increased metastatic potential, and an adverse prognosis. Although germline TP53 mutations significantly increase the risk of developing aggressive PCa, the impact of single-nucleotide polymorphisms (SNPs) remains less understood. This report presents a novel case of a patient diagnosed post-mortem with aggressive, metastatic PCa, with autopsy revealing a TP53 variant at codon 72 as the sole abnormality with confirmatory histology, immunohistochemistry, and next-generation sequencing. The arginine variant (R72) is known to have altered biochemical properties and may increase the risk of aggressive PCa development. The impact of this polymorphism on PCa risk has not been fully established and remains controversial. This report reviews the existing literature on the TP53 P72R polymorphism and its association with PCa risk. Although the exact biological significance remains to be defined, the presence of this SNP might indicate an increased risk for the development of aggressive PCa in patients.

Indexed as

genetic alterationimmunohistochemistrynext-generation sequencingp53p72r polymorphismprostate cancer

Identifiers

PMID41246646
PMCPMC12614195

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.