Recapitulation of the complex nerve–tumor–immune microenvironment is critical for understanding Peripheral Nerve Sheath Tumors (PNSTs). Conventional in vitro models and animal systems often struggle to model crucial intercellular and inter-organ communication with full physiological relevance, creating a bottleneck in discovering effective therapeutics. Organ-on-Chip (OoC) technologies offer a paradigm-shifting solution. These microengineered platforms precisely integrate human cell biology with controllable fluidic and mechanical cues to replicate tissue- and organ-level physiology, enabling real-time, quantitative monitoring of tissue dynamics. This review posits that OoC technology is poised to revolutionize PNST research. In this review, we summarize the development of advanced Tumor-Nerve-Immune-on-Chip systems that integrate patient-derived Schwann cells, immune components, and functional microvasculature. These systems will accurately model PNSTs. Adoption of OoC will enable a predictive and individualized experimental framework, accelerating therapeutic discovery and allowing for personalized drug prediction for these challenging diseases. • Defining the specific requirements and design space of next-gen PNST-on-chip platforms. • Organ-on-Chip technology mimics complex human nerve tumor environments. • Patient-specific models accelerate personalized drug discovery.
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William H. Delaney
Sara A. Faulkner
Wilbur A. Lam
Materials Today Advances
Emory University
Georgia Institute of Technology
The Wallace H. Coulter Department of Biomedical Engineering
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Delaney et al. (Thu,) studied this question.
www.synapsesocial.com/papers/69e31f9e40886becb653ecd7 — DOI: https://doi.org/10.1016/j.mtadv.2026.100770
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