Evidence map›Paper›PMID 41788117›Full record

ArticleCureus2026

Immunohistochemical Evaluation of p53 and Its Association With Prognostic Parameters in Breast Cancer.

K N Kusuma, Shetty Shilpa Madhav, Shankar S Vijay

Abstract read
In one paragraph

Article in Cureus, 2026. 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

3 authors.

K N KusumaDepartment of Pathology, Adichunchanagiri Institute of Medical Sciences, Adichunchanagiri University, Mandya, IND.
Shetty Shilpa MadhavDepartment of Pathology, Subbaiah Institute of Medical Sciences, Shimoga, IND.
Shankar S VijayDepartment of Pathology, Adichunchanagiri Institute of Medical Sciences, Adichunchanagiri University, Mandya, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background P53 is a tumour suppressor gene that is commonly altered in breast cancer, potentially affecting tumour behaviour and prognosis. However, the clinicopathological and molecular associations vary across studies. Hence, the present study aims to evaluate p53 positivity and its association with clinicopathological parameters and molecular subtypes in invasive breast carcinoma. Aims and objectives To evaluate p53 positivity in invasive breast carcinoma and analyse its association with key clinicopathological parameters. Methods A cross-sectional observational study was undertaken in the pathology department of a tertiary care hospital. Immunohistochemistry was used to measure p53 expression, which was then linked with clinicopathological features like tumour size, histological grade, lymph node status, lymphovascular invasion, hormone receptor status, human epidermal growth factor receptor 2 (HER2) status, Ki-67 proliferation index, and molecular subtype. Statistical analysis was done using SPSS software. Chi-square and Fisher's exact tests were used for correlation analysis, and p-values <0.05 were considered significant. Results P53 positivity was detected in 57.5% of the cases. P53 positivity was shown to be significantly associated with greater tumour size (p=0.029) and a high Ki-67 index (p=0.042) whereas histological grade, lymph nodal metastasis, lymphovascular invasion or hormone receptor status did not show statistical significance. Although hormone receptor-negative tumours showed more frequent p53 positivity status compared to a negative status, the results were not significant (p=0.052). P53 positivity was most frequent in aggressive molecular subtypes of tumours, like HER2-enriched (77.8%) and luminal B (75%) tumours. Conclusion P53 expression is associated with aggressive clinicopathological features like large tumour size, high Ki-67 index and the HER2-enriched subtype, suggesting its role in tumour progression and aggressiveness. Further, large multicentric studies with survival analysis are needed to confirm its clinical validity.

Indexed as

breast carcinomaimmunohistochemistryki-67molecular subtypep53

Identifiers

PMID41788117
PMCPMC12957401

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.