Microtissues®

Summary

Published in Biochemistry and Biophysics Reports (2024), this peer-reviewed study used 3D Petri Dish® micro-molds to form scaffold-free 3D microtissues. Full citation: Casali, Bruna Carla, et al. Blockage of αvβ3 integrin in 3D culture of triple-negative breast cancer and endothelial cells inhibits migration and discourages endothelial-to-mesenchymal plasticity

🧬 Oncology

Blockage of αvβ3 integrin in 3D culture of triple-negative breast cancer and endothelial cells inhibits migration and discourages endothelial-to-mesenchymal plasticity

Biochemistry and Biophysics Reports 2024 Casali, Bruna Carla, et al
Cite as: Casali, Bruna Carla, et al. Blockage of αvβ3 integrin in 3D culture of triple-negative breast cancer and endothelial cells inhibits migration and discourages endothelial-to-mesenchymal plasticity. Biochemistry and Biophysics Reports (2024). doi:10.1016/j.bbrep.2024.101686 doi.org/10.1016/j.bbrep.2024.101686

Research Overview

Triple-negative breast cancer carries a poor prognosis, and the integrin αvβ3 — upregulated in hypoxic TNBC models — helps drive the angiogenesis that feeds tumor progression. The disintegrin DisBa-01, a high-affinity αvβ3 blocker, had shown anti-tumoral and anti-angiogenic effects in 2D assays.

This study moved the question into 3D, investigating DisBa-01’s effects on endothelial and triple-negative breast cancer cells in spheroid models, where integrin-mediated adhesion, migration, and endothelial sprouting play out in a tissue-like architecture — a stiffer test of integrin blockade as an anti-angiogenic strategy.

Key Discoveries

  • Integrin αvβ3 blockade by DisBa-01 evaluated in 3D endothelial and TNBC models
  • 3D format captured integrin-mediated adhesion and migration dynamics of angiogenesis
  • Extends 2D anti-angiogenic findings toward tissue-like tumor models