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Updated: Oct 27, 2025

Tissue Engineering of a Human 3D in vitro Tumor Test System
Published on: August 6, 2013
Bioengineering a humanized 3D tri-culture osteosarcoma model to assess tumor invasiveness and therapy response
Cátia F Monteiro1, Catarina A Custódio1, João F Mano1
1CICECO - Aveiro Institute of Materials, University of Aveiro, Department of Chemistry, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal.
Abstract:
To date, anticancer therapies with evidenced efficacy in preclinical models fail during clinical trials. The shortage of robust drug screening platforms that accurately predict patient's response underlie these misleading results. To provide a reliable platform for tumor drug discovery, we herein propose a relevant humanized 3D osteosarcoma (OS) model exploring the potential of methacryloyl platelet lysates (PLMA)-based hydrogels to sustain spheroid growth and invasion. The architecture and synergistic cell-microenvironment interaction of an invading tumor was recapitulated encapsulating spheroids in PLMA hydrogels, alone or co-cultured with osteoblasts and mesenchymal stem cells. The stem cells alignment toward OS spheroid suggested that tumor cells chemotactically attracted the surrounding stromal cells, which supported tumor growth and invasion into the hydrogels. The exposure of established models to doxorubicin revealed an improved drug resistance of PLMA-based models, comparing with scaffold-free spheroids. The proposed OS models highlighted the feasibility of PLMA hydrogels to support tumor invasion and recapitulate tumor-stromal cell crosstalk, demonstrating the potential of this 3D platform for complex tumor modelling. STATEMENT OF SIGNIFICANCE: Cell invasion mechanisms involved in tumor progression have been recapitulated in the field of 3D in vitro modeling, leveraging the great advance in biomimetic materials. In line with the growing interest in human-derived biomaterials, the aim of this study is to explore for the first time the potential of methacryloyl platelet lysates (PLMA)-based hydrogels to develop a humanized 3D osteosarcoma model to assess tumor invasiveness and drug sensitivity. By co-culturing tumor spheroids with human osteoblasts and human mesenchymal stem cells, this study demonstrated the importance of the synergistic tumor cell-microenvironment interaction in tumor growth, invasion and drug resistance. The established 3D osteosarcoma model highlighted the feasibility of PLMA hydrogels as a relevant 3D platform for complex tumor modelling.
Insights
Developing a novel 3D osteosarcoma model using methacryloyl platelet lysates (PLMA)-based hydrogels improves drug screening accuracy. This humanized platform better predicts patient response by mimicking tumor invasion and cell crosstalk, advancing cancer drug discovery.
Area of Science:
- Biomaterials Science
- Cancer Biology
- Tissue Engineering
Background:
- Preclinical models often fail to predict clinical efficacy of anticancer therapies.
- A lack of robust drug screening platforms contributes to misleading results in cancer drug development.
- Accurate in vitro models are crucial for understanding tumor progression and drug resistance.
Purpose of the Study:
- To develop a humanized 3D osteosarcoma model using methacryloyl platelet lysates (PLMA)-based hydrogels.
- To assess the potential of PLMA hydrogels to sustain tumor spheroid growth and invasion.
- To evaluate the model's utility for drug screening and recapitulating tumor-stromal interactions.
Main Methods:
- Encapsulating osteosarcoma spheroids in PLMA hydrogels, with and without co-cultured osteoblasts and mesenchymal stem cells.
- Utilizing 3D in vitro modeling to mimic tumor architecture and cell-microenvironment interactions.
- Exposing established 3D models to doxorubicin to assess drug sensitivity and resistance.
Main Results:
- PLMA hydrogels successfully sustained osteosarcoma spheroid growth and invasion, mimicking a 3D tumor microenvironment.
- Co-culture with stromal cells (osteoblasts, mesenchymal stem cells) demonstrated tumor cell chemotaxis and supported tumor progression.
- The 3D model exhibited enhanced doxorubicin resistance compared to scaffold-free spheroids, highlighting its predictive potential.
Conclusions:
- PLMA-based hydrogels provide a feasible and relevant platform for complex 3D osteosarcoma modeling.
- The model effectively recapitulates tumor invasion, tumor-stromal cell crosstalk, and drug resistance.
- This humanized 3D platform holds significant potential for advancing preclinical cancer drug discovery and improving treatment prediction.
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