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.

Acta Biomaterialia
|July 24, 2021
PubMed

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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