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Updated: Jan 16, 2026

Generation of High-Throughput Three-Dimensional Tumor Spheroids for Drug Screening
Published on: September 5, 2018
High-throughput 3D engineered paediatric tumour models for precision medicine
MoonSun Jung1,2, Valentina Poltavets1,3,4, Joanna N Skhinas1,4
1Children's Cancer Institute, Lowy Cancer Research Centre, UNSW Sydney, Sydney, NSW, 2052, Australia.
Abstract:
Precision medicine for paediatric and adult cancers that incorporates drug sensitivity profiling can identify effective therapies for individual patients. However, obtaining adequate biopsy samples for high-throughput (HTP) screening remains challenging, with tumours needing to be expanded in culture or patient-derived xenografts, this is time-consuming and often unsuccessful. Herein, we have developed paediatric patient-derived tumour models using an engineered extracellular matrix (ECM) tissue mimic hydrogel system and HTP 3D bioprinting. Gene expression analysis from a neuroblastoma and sarcoma paediatric patient cohort identified key components of the ECM in these tumour types. Engineered hydrogels with ECM-mimic peptides were used to bioprint and create patient-specific tumouroids using patient-derived cells from xenograft models, and the approach was further confirmed on direct patient tumour samples. Bioprinted tumouroids from the PDX models recapitulated the genetic and phenotypic characteristics of the original tumours and retained tumourigenicity. HTP drug screening of these models identified individualised drug sensitivities. Our approach offers a timely and clinically relevant technology platform for precision medicine in paediatric cancers, potentially transforming preclinical testing across multiple cancer types.
Insights
Researchers developed patient-specific tumouroids using 3D bioprinting and engineered hydrogels. This precision medicine approach enables rapid drug sensitivity testing for paediatric cancers, overcoming traditional sample limitations.
Area of Science:
- Oncology
- Biotechnology
- Materials Science
Background:
- Precision medicine requires effective drug sensitivity profiling for personalized cancer therapy.
- Current methods for generating patient-derived tumour models for high-throughput (HTP) screening are time-consuming and often unsuccessful.
- Obtaining adequate biopsy samples for HTP screening presents a significant challenge in paediatric oncology.
Purpose of the Study:
- To develop a novel platform for creating patient-specific paediatric tumour models.
- To overcome limitations in sample acquisition and model generation for precision medicine in paediatric cancers.
- To enable rapid and accurate drug sensitivity profiling for individualised cancer treatment.
Main Methods:
- Utilized gene expression analysis of paediatric neuroblastoma and sarcoma cohorts to identify key extracellular matrix (ECM) components.
- Engineered hydrogel systems incorporating ECM-mimic peptides for 3D bioprinting.
- Created patient-specific tumouroids using patient-derived cells from xenograft models and direct patient tumour samples.
Main Results:
- Bioprinted tumouroids successfully recapitulated the genetic and phenotypic characteristics of original tumours, including tumourigenicity.
- The engineered ECM hydrogel system facilitated the creation of patient-specific tumouroids.
- High-throughput drug screening on these tumouroids identified individualised drug sensitivities.
Conclusions:
- Developed a timely and clinically relevant technology platform for precision medicine in paediatric cancers.
- The 3D bioprinting approach using engineered ECM hydrogels offers a viable alternative to traditional tumour model generation.
- This platform has the potential to transform preclinical testing and advance personalised treatment strategies for various paediatric cancers.
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