3D bioprinted breast cancer model reveals stroma-mediated modulation of extracellular matrix and radiosensitivity

Deciphering breast cancer treatment resistance remains hindered by the lack of models that can successfully capture the four-dimensional dynamics of the tumor microenvironment. Here, we show that microextrusion bioprinting can reproducibly generate distinct cancer and stromal compartments integrating cells relevant to human pathology. Our findings unveil the functional maturation of this millimeter-sized model, showcasing the development of a hypoxic cancer core and an increased surface proliferation. Maturation was also driven by the presence of cancer-associated fibroblasts (CAF) that induced elevated microvascular-like structures complexity. Such modulation was concomitant to extracellular matrix remodeling, with high levels of collagen and matricellular proteins deposition by CAF, simultaneously increasing tumor stiffness and recapitulating breast cancer fibrotic development. Importantly, our bioprinted model faithfully reproduced response to treatment, further modulated by CAF. Notably, CAF played a protective role for cancer cells against radiotherapy, facilitating increased paracrine communications. This model holds promise as a platform to decipher interactions within the microenvironment and evaluate stroma-targeted drugs in a context relevant to human pathology.

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Publication Details

Journal
Bioactive Materials
Published
2024-09-05
DOI
https://doi.org/10.1016/j.bioactmat.2024.08.037
Citations
13
Primary Topic
Cancer Cells and Metastasis
Type
article
Field-Weighted Citation Impact
3.67

Funders

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article

3D bioprinted breast cancer model reveals stroma-mediated modulation of extracellular matrix and radiosensitivity

Marie‐Laure Stachowicz, Jean‐Christophe Fricain, Léo Comperat, Jean‐William Dupuy et al.
13 citations
Bioactive Materials
Cancer Cells and Metastasis
3.67
article

3D bioprinted breast cancer model reveals stroma-mediated modulation of extracellular matrix and radiosensitivity

Marie‐Laure Stachowicz, Jean‐Christophe Fricain, Léo Comperat, Jean‐William Dupuy, Nathalie Dusserre, Anthony Vial, Hugo Oliveira, Theo Desigaux, Michaël Molinari, François Paris, Malou Lea
article en
13 citations

Abstract

Deciphering breast cancer treatment resistance remains hindered by the lack of models that can successfully capture the four-dimensional dynamics of the tumor microenvironment. Here, we show that microextrusion bioprinting can reproducibly generate distinct cancer and stromal compartments integrating cells relevant to human pathology. Our findings unveil the functional maturation of this millimeter-sized model, showcasing the development of a hypoxic cancer core and an increased surface proliferation. Maturation was also driven by the presence of cancer-associated fibroblasts (CAF) that induced elevated microvascular-like structures complexity. Such modulation was concomitant to extracellular matrix remodeling, with high levels of collagen and matricellular proteins deposition by CAF, simultaneously increasing tumor stiffness and recapitulating breast cancer fibrotic development. Importantly, our bioprinted model faithfully reproduced response to treatment, further modulated by CAF. Notably, CAF played a protective role for cancer cells against radiotherapy, facilitating increased paracrine communications. This model holds promise as a platform to decipher interactions within the microenvironment and evaluate stroma-targeted drugs in a context relevant to human pathology.

Bioactive MaterialsVol. 42
Centre National de la Recherche Scientifique (FR), Université de Bordeaux (FR), Inserm (FR), Centre Hospitalier Universitaire de Bordeaux (FR), Institut de Cancérologie de l'Ouest (FR), Bordeaux Population Health (FR), Chimie et Biologie des Membranes et des Nanoobjects (FR), Institut Européen de Chimie et Biologie (FR), Institut Polytechnique de Bordeaux (FR), Laboratory for the Bioengineering of Tissues (FR), Nantes Université (FR)
Institut National de la Santé et de la Recherche Médicale, Fondation ARC pour la Recherche sur le Cancer
Openalex Percentile: Top 5%
Cancer Cells and Metastasis
3.67
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