Evidence map›Paper›PMID 39157839›Full record

ArticleJournal of oral and maxillofacial pathology : JOMFP

Immunoexpression of CD44, p16 and VEGF in oral cancer.

Priscila Marinho de Abreu, Marcella Sol, Patrícia Roccon Bianchi Molini, Camila Batista Daniel, Danielle Resende Camisasca, Sandra Ventorin von Zeidler

Abstract read
In one paragraph

Article in Journal of oral and maxillofacial pathology : JOMFP. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

  1. Review
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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

6 authors.

Priscila Marinho de AbreuBiotechnology Program, Universidade Federal do Espírito Santo - UFES, Vitória, ES, Brazil.
Marcella SolDepartment of Pathology, Universidade Federal do Espírito Santo - UFES, Vitória, ES, Brazil.
Patrícia Roccon Bianchi MoliniSchool of Dentistry, Universidade Federal do Espírito Santo - UFES, Vitória, ES, Brazil.
Camila Batista DanielBiotechnology Program, Universidade Federal do Espírito Santo - UFES, Vitória, ES, Brazil.
Danielle Resende CamisascaSchool of Dentistry, Universidade Federal do Espírito Santo - UFES, Vitória, ES, Brazil.
Sandra Ventorin von ZeidlerBiotechnology Program, Universidade Federal do Espírito Santo - UFES, Vitória, ES, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: The aim of the present study was to examine the immunoexpression of CD44, p16 and VEGF in oral squamous cell carcinoma (OSCC) and correlate them to clinicopathological parameters and survival outcomes in order to clarify their prognostic impact. Material and Methods: A total of 68 individuals with OSCC recruited between 2011 and 2015 from two referral centres were enrolled in the study. The samples were placed on silanized glass slides and subjected to immunohistochemistry using anti-p16, anti-CD44 and anti-VEGF antibodies. The H Score was used for p16 and VEGF, while CD44 was scored according to the percentage of stained cells. Chi-square tests and Fisher's exact probability tests were used to compare clinicopathological characteristics according to the immunohistochemical expression, while overall survival and disease-free survival were estimated and compared using the Kaplan-Meier method and log-rank test, respectively. For all hypothesis tests, the level of significance was set at Results: No correlation was observed between the expression of tumour VEGF, p16 and CD44, and the clinicopathological characteristics analysed. Patients with high stromal VEGF expression had better disease-free survival than patients with low VEGF expression ( Conclusion: In summary, P16, CD44 and tumour VEGF did not prove to be good prognostic biomarkers. Stromal VEGF expression is suggested to be a good candidate prognostic biomarker, although additional studies are needed.

Indexed as

Biomarkeroral squamous cell carcinomaprognosisVEGF

Identifiers

PMID39157839
PMCPMC11329094

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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.