Abstract
Over the past decade, organoid technology has emerged as a transformative tool in biomedical research, enabling the development of physiologically relevant models of both healthy and malignant tissues. While this technology has substantially advanced our understanding of adult cancers, its application in pediatric oncology remains limited. Pediatric tumors are not only biologically distinct from adult malignancies but also present a lower incidence, posing additional challenges for model development. Despite these obstacles, recent efforts have led to the successful generation of organoids from various pediatric tumor types, offering new opportunities to explore disease mechanisms and therapeutic responses in a patient-specific manner. In this Review, we summarize recent advances in organoid technology in pediatric cancer research, with a focus on its applications in preclinical and translational research. We also discuss current limitations and highlight emerging innovations that hold promise for further refining pediatric cancer models.
| Original language | English |
|---|---|
| Journal | FEBS Letters |
| DOIs | |
| Publication status | E-pub ahead of print - 14 Oct 2025 |
Bibliographical note
Publisher Copyright:© 2025 The Author(s). FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.
Funding
The authors thank M. Dings for the critical reading of the manuscript. We are grateful for support from the Dutch Research Council (NWO-Vidi#203.003) and the Children Cancer Free Foundation (KiKa).r No Statement Available
| Funders | Funder number |
|---|---|
| Stichting Kinderen Kankervrij | |
| Nederlandse Organisatie voor Wetenschappelijk Onderzoek | 203.003 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- in vitro modeling
- pediatric cancer
- preclinical models
- tumor organoids
- tumoroid
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