Evidence map›Paper›PMID 42643993›Full record

ArticleCureus2026

The Diagnostic and Prognostic Utility of Heat Shock Protein 27 as a Biomarker for Oral Squamous Cell Carcinoma.

Katy Flannery, Maryam Salik, Hilal Arnouk

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
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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.

Katy FlanneryPathology, Midwestern University Chicago College of Osteopathic Medicine, Downers Grove, USA.
Maryam SalikPathology and Laboratory Medicine, Midwestern University Chicago College of Osteopathic Medicine, Downers Grove, USA.
Hilal ArnoukPathology, Illinois College of Osteopathic Medicine, The Chicago School, Chicago, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective Despite multiple studies on the involvement of heat shock protein 27 (HSP27) in cancer progression in oral squamous cell carcinoma (OSCC), there is a lack of overall consensus on its expression trends in this type of cancer. In this study, we examined the differential expression of HSP27 in tissue samples of oral cancer and the normal oral mucosa. Additionally, we correlated HSP27 expression with crucial clinicopathological parameters, including clinical staging and histopathological grading. Our findings suggest that HSP27 is a potential biomarker that can aid in the diagnosis and prognosis of patients suffering from oral cancer. Study design Immunohistochemistry was performed to detect HSP27 in both normal oral mucosa and OSCC from a variety of clinical stages and histopathological grades. Samples then underwent imaging followed by computer-assisted image analysis to objectively quantify the data. Results The HSP27 immunohistochemical detection coupled with computer-assisted image analysis documented a significant increase in HSP27 expression in OSCC tissue samples compared to normal oral mucosa tissue samples. Its expression analysis also showed correlations with the nodal status, clinical stage, and histopathological grade. Conclusion This study examined HSP27 expression patterns in oral cancer tissue samples and found HSP27 to be upregulated in OSCC compared to the normal oral mucosa. Additionally, HSP27 expression significantly correlated with the histopathological grade, nodal status, and the overall clinical stage. This study paves the way for the potential use of HSP27 as a supplementary diagnostic and prognostic tool in evaluating and monitoring disease progression in oral cancer patients.

Indexed as

diagnostic biomarkerhead and neck cancerhsp27oral squamous cell carcinomaprognostic biomarkertumor progression

Identifiers

PMID42643993
PMCPMC13506219

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Registered trials

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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.