Evidence map›Paper›PMID 42041729›Full record

Observational studyCurrent oncology (Toronto, Ont.)2026

Co-Occurrence of Nuclear-Catenin and H3K27me3 Expression in Advanced Colorectal Cancer: A Retrospective Observational Study.

Ramona Abrudan, Luca Abrudan, Andreea Cămărășan, Ovidiu Camarasan, Corina Florica Ioniță, Luca Vilceanu, Ovidiu Laurean Pop

Abstract readObservational Study
In one paragraph

Observational study in Current oncology (Toronto, Ont.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. In Vitro Effects ofInternational journal of microbiology · 2026
    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

7 authors.

Ramona AbrudanDepartemnt of Psychoneurosciences and Rehabilitation, Medicine and Pharmacy Faculty, University of Oradea, 410087 Oradea, Romania.
Luca AbrudanRadiation Oncology, Radiotherapy Laboratory, County Clinical Emergency Hospital Bihor, 410087 Oradea, Romania.
Andreea CămărășanDepartment of Morphological Disciplines, Medicine and Pharmacy Faculty, University of Oradea, 410087 Oradea, Romania.ORCID 0000-0002-1557-7756
Ovidiu CamarasanProf. Dr. Ioan Pușcaș Hospital Șimleu Silvaniei, 455300 Șimleu Silvaniei, Romania.
Corina Florica IonițăDepartment of Oncology, Topmed Hospital, 540156 Târgu Mureș, Romania.
Luca VilceanuFaculty of Medicine, University of Oradea, 410087 Oradea, Romania.
Ovidiu Laurean PopDepartment of Morphological Disciplines, Medicine and Pharmacy Faculty, University of Oradea, 410087 Oradea, Romania.

Funding

University of Oradea 10
6 · The paper itself

Abstract

Colorectal cancer is a heterogeneous malignancy characterized by alterations in oncogenic signaling pathways and epigenetic mechanisms involved in gene regulation. Aberrant activation of the Wnt/β-catenin pathway represents a central molecular event in colorectal tumorigenesis, while histone-associated epigenetic modifications may contribute to tumor progression and variability. This study aimed to investigate the relationship between Wnt pathway activation and histone H3 lysine 27 trimethylation in colorectal cancer and to examine their associations with clinicopathological and molecular characteristics. A retrospective observational study was performed on 83 colorectal adenocarcinoma cases using immunohistochemical evaluation of nuclear β-catenin and H3K27me3 expression in formalin-fixed, paraffin-embedded tumor samples, together with molecular analysis of KRAS, NRAS, and BRAF mutations and microsatellite instability status. Nuclear β-catenin expression was observed in 39.8% of cases, while H3K27me3 exhibited negative, mosaic, or diffuse nuclear staining patterns. Nuclear β-catenin expression was significantly associated with patient sex and age, whereas H3K27me3 expression patterns were significantly associated with tumor location, histological grade, disease stage, and metastatic status. These results indicate that Wnt pathway activation and H3K27me3-associated epigenetic alterations frequently coexist in colorectal cancer and support the value of integrated molecular and epigenetic assessment.

Indexed as

beta CateninColorectal NeoplasmsHistonesAgedAged, 80 and overCell NucleusEpigenesis, GeneticFemaleHumansMaleMiddle AgedRetrospective StudiesWnt Signaling Pathwaybeta CateninCTNNB1 protein, humanHistonescolorectal cancerepigeneticH3K27me3Wnt/β-catenin pathway

Identifiers

PMID42041729
PMCPMC13114889

What Socratic 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 Socratic graph.