Evidence map›Paper›PMID 39052015›Full record

ArticleBiomolecules & biomedicine2024

Epiplakin expression dynamics during colon carcinogenesis: Correlation with proliferation.

Damla Gül Fındık, Erhan Şahin, Özlem Türelik, Gürkan Güneri

Abstract read
In one paragraph

Article in Biomolecules & biomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

4 authors.

Damla Gül FındıkDepartment of Histology and Embryology, Faculty of Medicine, Bilecik Şeyh Edebali University, Bilecik, Turkey.
Erhan ŞahinDepartment of Histology and Embryology, Faculty of Medicine, Bilecik Şeyh Edebali University, Bilecik, Turkey.
Özlem TürelikDepartment of Pathology, Faculty of Medicine, Bilecik Şeyh Edebali University, Bilecik, Turkey.
Gürkan GüneriDepartment of General Surgery, Faculty of Medicine, Bilecik Şeyh Edebali University, Bilecik, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer poses a significant global health challenge, with a considerable proportion arising from colon adenomas. Understanding the molecules involved in the carcinogenesis process is crucial for improving colon cancer diagnosis and prognosis. While research on the role of epiplakin in cancer remains limited compared to other plakin group proteins, comprehending its expression patterns and correlations can offer valuable insights into colon carcinogenesis. In this study, we analyzed 60 tissue samples, including colon adenocarcinomas, tubular adenomas (low malignancy risk group), tubulovillous adenomas (high malignancy risk group), and adjacent normal colon tissues. Classification and grading were reevaluated by histological examination. Immunohistochemistry was performed to assess epiplakin and Ki67 expression. Epiplakin optical density and the Ki67 proliferation index were calculated using ImageJ. Statistical analyses were conducted to evaluate correlations and significance. Epiplakin expression was significantly decreased in colon adenocarcinomas [optical density median 4.04 (95% CI, 3.98 to 4.24)] and tubulovillous adenomas [4.32 (95% CI, 4.08 to 4.32)] compared to normal colon tissues [4.61 (95% CI, 4.50 to 4.67)] and tubular adenomas [4.87 (95% CI, 4.67 to 4.88)] (P < 0.05). Moreover, adenoma groups exhibited higher proliferation indices (P < 0.05), and a positive correlation was found between epiplakin expression and the Ki67 proliferation index (r = 0.317, P < 0.05). Our study highlights the potential significance of epiplakin in colorectal cancer. Decreased epiplakin expression is associated with colon malignancy progression, suggesting its role as a potential marker.

Indexed as

AdenomaCarcinogenesisCell ProliferationColonic NeoplasmsKi-67 AntigenAdenocarcinomaAgedBiomarkers, TumorColonFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedBiomarkers, TumorKi-67 Antigen

Identifiers

PMID39052015
PMCPMC11647249

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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.