Evidence map›Paper›PMID 40521787›Full record

ArticleThe Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology2025

Epigenetics and Expression of the Wnt Signaling Pathway in Ulcerative Colitis.

Zuhal Altintas, Mehmet Emin Erdal, Engin Altintas

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Article in The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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.

Zuhal AltintasDepartment of Medical Genetics, Mersin University Faculty of Medicine, Mersin, Türkiye.
Mehmet Emin ErdalDepartment of Medical Biology and Genetics, Mersin University Faculty of Medicine, Mersin, Türkiye.
Engin AltintasDepartment of Gastroenterology, Mersin University Faculty of Medicine, Mersin, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aims: Secreted frizzled-related proteins (SFRPs) are antagonists that bind Wnt and inhibit signaling through this pathway. Secreted frizzled-related proteins are silenced by promoter methylation and cause hyperactivation of the Wnt pathway. In this study, the aim was to evaluate the relationship between methylation and expression of genes involved in the Wnt signaling pathway and the risk of cancer development in inflammatory bowel disease. Materials and Methods: The patient group consisted of 20 individuals who were diagnosed with left-side ulcerative colitis and underwent surveillance colonoscopy; the control group consisted of 15 individuals without symptoms and endoscopic pathology who were screened for colorectal cancer. Tissue samples were obtained from inflamed and non-inflamed areas of the colon. Methylation and gene expression profiles of the Wnt pathway genes APC1A, APC2, SFRP1, SFRP2, SFRP4, and SFRP5 were analyzed from DNA and RNA obtained from these tissues. Results: A significant correlation was found between the methylation status and expression of the SFRP4 gene in the proximal colon in the patient group compared to controls (P = .018). For the methylation of the APC2 gene, 8 patients were methylated (40%), and 12 were unmethylated (60%), while 1 of the controls was methylated (6.7%) and 14 were unmethylated (93.3%) (P = .018). There was no statistically significant association between methylation, expression, and inflammation status for other genes between patients and controls. Conclusion: In ulcerative colitis, inflammation is thought to be associated with both increased APC2 methylation and decreased expression findings due to decreased SFRP4 methylation in non-inflamed areas. However, more research is needed to establish a link with ulcerative colitis-related neoplasia.

Indexed as

Colitis, UlcerativeDNA MethylationEpigenesis, GeneticWnt Signaling PathwayAdaptor Proteins, Signal TransducingAdultAgedCase-Control StudiesColonColorectal NeoplasmsFemaleHumansIntercellular Signaling Peptides and ProteinsMaleMembrane ProteinsMiddle AgedAdaptor Proteins, Signal TransducingIntercellular Signaling Peptides and ProteinsMembrane ProteinsProto-Oncogene ProteinsSecreted Frizzled-Related ProteinsSFRP1 protein, humanSFRP2 protein, humanSFRP4 protein, humanSFRP5 protein, humanDNA methylationinflammatory bowel diseaseulcerative colitisWnt pathway

Identifiers

PMID40521787
PMCPMC12351295

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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.