Evidence map›Paper›PMID 40562819›Full record

ReviewOncogene2025

Post-transcriptional control of gene expression by β-catenin: expanding the non-canonical ARMoury.

O Sevim, H Park, R G Morgan

Abstract readReview
In one paragraph

Review in Oncogene, 2025. 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. Article
  2. Review
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.

O Sevim *School of Life Sciences, University of Sussex, Brighton, UK.ORCID http://orcid.org/0000-0002-3348-3913
H Park *Brighton & Sussex Medical School, University of Sussex, Brighton, UK. hyun.park@nhs.net.ORCID http://orcid.org/0009-0002-1895-2504
R G Morgan *School of Life Sciences, University of Sussex, Brighton, UK.ORCID http://orcid.org/0000-0003-0429-6294

Funding

Children's Cancer and Leukaemia Group (CCLG) CCLGA 2023 16 MorganKay Kendall Leukaemia Fund (KKLF) KKL1051/KKL1446Worldwide Cancer Research 25-0321
6 · The paper itself

Abstract

The Wnt/β-catenin pathway is an evolutionarily conserved signal transduction cascade with critical regulatory roles in cellular proliferation, cell fate determination and tissue homeostasis. Through the regulation of multiple human stem cell systems, canonical Wnt signalling is not only a major contributor to normal development, but also heavily implicated in a multitude of human diseases, including cancer. The central mediator of the pathway β-catenin, first identified as Armadillo (ARM) in Drosophila, has well-defined roles in cell adhesion and transcription within the pathway. However, accumulating evidence suggests β-catenin functionality is more complex than initially anticipated with reported roles beyond those historically characterised, including the regulation of RNA and RNA-binding proteins (RBP). This review will summarise the current understanding around β-catenin as a post-transcriptional regulator in normal and malignant development, drawing particular attention to cell types not traditionally used to characterise Wnt signalling but uniquely placed to reveal novel β-catenin function.

Indexed as

beta CateninGene Expression RegulationWnt Signaling PathwayAnimalsArmadillo Domain ProteinsHumansNeoplasmsRNA-Binding ProteinsArmadillo Domain Proteinsbeta CateninRNA-Binding Proteins

Identifiers

PMID40562819
PMCPMC12256263

What OpenQuestion 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 OpenQuestion graph.