Chondrosarcoma Co-Culture 3D Model─An Insight to Evaluate Drugs Acting on TAMs

Chondrosarcoma (CHS), also known as malignant cartilage tumors, is the second most common bone cancer after osteosarcoma. This tumor is particularly chemo- and radioresistant, and the only therapeutic alternative is surgery with wide margins. The tumor immune microenvironment reveals an infiltration of tumor-associated macrophages (TAMs) sometimes approaching 50% of the tumor mass, mainly differentiated into M2-like phenotype and correlated with poor prognosis and metastasis. Thus, macrophage-targeting therapies could have an interest in the management of CHS. To evaluate these strategies, we propose here the development of a three-dimensional (3D) tumoroid co-culture model between two human CHS cell lines (JJ012 and CH2879) and a human leukemia monocytic cell line (THP-1) in a methylcellulose matrix. These two models were compared to the in vivo xenograft models in terms of macrophage phenotypes, proteoglycans, MMP-9, and COX-2 expression. Finally, mifamurtide, an immunomodulator acting on TAMs, was evaluated on the most in vitro relevant model: 3D co-culture CH2879 model. Our results showed that it is now possible to develop 3D models that very accurately mimic what is found in vivo with the possibility of evaluating treatments specific to a tumor cell component.

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Publication Details

Journal
ACS Biomaterials Science & Engineering
Published
2024-08-09
DOI
https://doi.org/10.1021/acsbiomaterials.4c00625
Citations
4
Primary Topic
Immune cells in cancer
Type
article
Field-Weighted Citation Impact
0.96

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article

Chondrosarcoma Co-Culture 3D Model─An Insight to Evaluate Drugs Acting on TAMs

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4 citations
ACS Biomaterials Science & Engineering
Immune cells in cancer
0.96
article

Chondrosarcoma Co-Culture 3D Model─An Insight to Evaluate Drugs Acting on TAMs

Christelle Blavignac, Emmanuel Moreau, Emmanuel Chautard, Caroline Peyrode, Rohan Quoniou, Elisa Bortoli, Florent Cachin
article en
4 citations

Abstract

Chondrosarcoma (CHS), also known as malignant cartilage tumors, is the second most common bone cancer after osteosarcoma. This tumor is particularly chemo- and radioresistant, and the only therapeutic alternative is surgery with wide margins. The tumor immune microenvironment reveals an infiltration of tumor-associated macrophages (TAMs) sometimes approaching 50% of the tumor mass, mainly differentiated into M2-like phenotype and correlated with poor prognosis and metastasis. Thus, macrophage-targeting therapies could have an interest in the management of CHS. To evaluate these strategies, we propose here the development of a three-dimensional (3D) tumoroid co-culture model between two human CHS cell lines (JJ012 and CH2879) and a human leukemia monocytic cell line (THP-1) in a methylcellulose matrix. These two models were compared to the in vivo xenograft models in terms of macrophage phenotypes, proteoglycans, MMP-9, and COX-2 expression. Finally, mifamurtide, an immunomodulator acting on TAMs, was evaluated on the most in vitro relevant model: 3D co-culture CH2879 model. Our results showed that it is now possible to develop 3D models that very accurately mimic what is found in vivo with the possibility of evaluating treatments specific to a tumor cell component.

ACS Biomaterials Science & EngineeringVol. 10(9)
Inserm (FR), Université Clermont Auvergne (FR), Centre Jean Perrin (FR), Centre Hospitalier Universitaire de Clermont-Ferrand (FR), Imagerie Moléculaire et Stratégies Théranostiques
Institut National de la Santé et de la Recherche Médicale, Université Clermont-Auvergne
Zero hunger
Openalex Percentile: Top 25%
Immune cells in cancer
0.96
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