# Roles and regulation of δ-catenin in tumorigenesis and neuronal diseases

**Authors:** Yang Zhang, Keping Xie, Tingting Jiang

PMC · DOI: 10.3389/fcell.2025.1559059 · Frontiers in Cell and Developmental Biology · 2025-03-27

## TL;DR

This paper reviews the role of δ-catenin in neurological diseases and cancer, highlighting its potential as a diagnostic and therapeutic biomarker.

## Contribution

The paper provides a comprehensive review of CTNND2's signaling functions and its relevance to neuro-related diseases and cancers.

## Key findings

- CTNND2 is linked to neurological disorders like autism and Alzheimer's.
- δ-catenin is involved in cancer progression and could serve as a biomarker.
- The paper identifies gaps in current research on CTNND2 signaling.

## Abstract

CTNND2 gene is located on the short arm of human chromosome 5 and encodes δ-catenin protein, which interacts with different proteins and plays different cell functions. Studies have demonstrated that δ-catenin plays an important role in regulating synaptic maturation and neuronal integrity. The CTNND2 gene is closely associated with a variety of neurological diseases, including Cri-du-Chat syndrome, Autism spectrum disorders, Alzheimer’s disease, and Epilepsy. Furthermore, an increasing number of studies have demonstrated that CTNND2 is involved in various cancers and may serve as a novel biomarker for the diagnosis and treatment for these diseases. In this review, we will focus on the signaling regulatory functions of CTNND2 and its encoded protein δ-catenin in neuro-related diseases and cancers, and discuss the limitations of previous investigative studies and the challenges of the future researches on CTNND2 and δ-catenin signaling.

## Linked entities

- **Genes:** CTNND2 (catenin delta 2) [NCBI Gene 1501]
- **Diseases:** Cri-du-Chat syndrome (MONDO:0007404), Alzheimer’s disease (MONDO:0004975), Epilepsy (MONDO:0005027)

## Full-text entities

- **Genes:** CTNND2 (catenin delta 2) [NCBI Gene 1501] {aka GT24, NPRAP}
- **Diseases:** cancers (MESH:D009369), neurological diseases (MESH:D020271), Autism spectrum disorders (MESH:D000067877), Alzheimer's disease (MESH:D000544), Cri-du-Chat syndrome (MESH:D003410), neuronal diseases (MESH:D016472), neuro-related diseases (MESH:C536203), Epilepsy (MESH:D004827), tumorigenesis (MESH:D063646)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11983503/full.md

## References

117 references — full list in the complete paper: https://tomesphere.com/paper/PMC11983503/full.md

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Source: https://tomesphere.com/paper/PMC11983503