Assessing spheroid viability in high throughput

Sabrina Forveille1, Flora Doffe1, Marion Leduc1

  • 1Centre de Recherche des Cordeliers, Inserm UMRS 1138, Sorbonne Université, Université Paris Cité, Équipe labellisée par la Ligue contre le Cancer, Institut Universitaire de France, Paris, France; INSERM US23/CNRS UAR 3655, Metabolomics and Cell Biology Platforms, Institut Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Insights

This study introduces an advanced image-based phenotypic 3D high-throughput screening (HTS) assay. This method uses specialized labware for spheroid formation, enhancing cancer drug discovery with more relevant tumor models.

Area of Science:

  • Oncology
  • Drug Discovery
  • Biotechnology

Background:

  • Phenotypic two-dimensional (2D) high-throughput screening (HTS) is crucial for anticancer drug discovery.
  • Advances in automation and imaging enable image-based HTS in 3D cell cultures.
  • Three-dimensional (3D) models better mimic tumor physiology and microenvironment.

Purpose of the Study:

  • To present an image-based phenotypic 3D HTS assay.
  • To utilize novel imaging-compatible labware for spheroid formation.
  • To advance oncological drug discovery with more relevant models.

Main Methods:

  • Development of an image-based phenotypic 3D HTS assay.
  • Utilization of specialized imaging-compatible labware.
  • Spheroid formation for 3D cell culture models.

Main Results:

  • Successful implementation of an image-based phenotypic 3D HTS assay.
  • Demonstrated utility of imaging-compatible labware for spheroid culture.
  • Established a more physiologically relevant platform for drug screening.

Conclusions:

  • The developed 3D HTS assay offers a more accurate platform for oncological drug discovery.
  • Image-based 3D screening facilitates the development of novel anticancer agents.
  • This approach advances the translation of preclinical findings to clinical applications.

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