# Epigenetic crosstalk in neuroblastoma development and progression

**Authors:** Nathan Drolet, Amber Wolf, Joanna Yi, Eveline Barbieri

PMC · DOI: 10.3389/fcell.2026.1769372 · Frontiers in Cell and Developmental Biology · 2026-03-11

## TL;DR

This paper explores how epigenetic mechanisms influence the development and progression of neuroblastoma, a type of childhood cancer.

## Contribution

The study provides new insights into the interplay between developmental pathways and epigenetic control in neuroblastoma.

## Key findings

- Epigenetic crosstalk plays a key role in neuroblastoma differentiation and oncogenesis.
- Targeted therapies against epigenetic regulators show promise for improving patient outcomes.

## Abstract

Neuroblastoma (NB), a pediatric malignancy of the peripheral nervous system, accounts for 15% of pediatric cancer deaths and remains a major challenge for cancer therapy. NB originates from sympathoadrenal (SA) progenitors of the neural crest (NC) cell lineage, whose formation and differentiation are controlled by epigenetic mechanisms. Although signaling pathways and epigenetic factors implicated in NB tumorigenesis have been well-described, a holistic understanding of how development and epigenetics overlap to drive NB is lacking. By exploring vital interplays and co-dependencies between key pathways and their epigenetic control in NC development, we have gained novel insights into the mechanisms governing NB differentiation and oncogenesis. These converging insights have enabled the application of targeted therapies against epigenetic regulators driving NB with promising implications for patient outcomes.

## Linked entities

- **Diseases:** neuroblastoma (MONDO:0005072)

## Full-text entities

- **Diseases:** tumorigenesis (MESH:D063646), NB (MESH:D009447), cancer (MESH:D009369)
- **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/PMC13013432/full.md

## References

186 references — full list in the complete paper: https://tomesphere.com/paper/PMC13013432/full.md

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Source: https://tomesphere.com/paper/PMC13013432