TY - JOUR
T1 - Establishment of patient-derived 3D in vitro models of sarcomas
T2 - literature review and guidelines on behalf of the FORTRESS working group
AU - De Cock, Lore
AU - Palubeckaitė, Ieva
AU - Bersani, Francesca
AU - Faehling, Tobias
AU - Pasquali, Sandro
AU - Umbaugh, Sam
AU - Meister, Michael Torsten
AU - Danks, Molly R.
AU - Manasterski, Piotr
AU - Miallot, Richard
AU - Krumbholz, Manuela
AU - Roohani, Siyer
AU - Heymann, Dominique
AU - Cidre-Aranaz, Florencia
AU - Wozniak, Agnieszka
AU - Schöffski, Patrick
AU - Bovée, Judith V.M.G.
AU - Merlini, Alessandra
AU - Venneker, Sanne
N1 - Copyright © 2025. Published by Elsevier Inc.
PY - 2025/7
Y1 - 2025/7
N2 - Sarcomas are a large family of rare and heterogeneous mesenchymal tumors, which respond poorly to available systemic treatments. Translation of preclinical findings into clinical applications has been slow, limiting improvements in patients’ outcomes and ultimately highlighting the need for a better understanding of sarcoma biology to develop more effective, subtype-specific therapies. To this end, reliable preclinical models are crucial, but the development of 3D in vitro sarcoma models has been lagging behind that of epithelial cancers. This is primarily due to the rarity and heterogeneity of sarcomas, and lack of widespread knowledge regarding the optimal growth conditions of these in vitro models. In this review, we provide an overview of currently available sarcoma tumoroid models, together with guidelines and suggestions for model development and characterization, on behalf of the FORTRESS (Forum For Translational Research in Sarcomas) international research working group on 3D sarcoma models.
AB - Sarcomas are a large family of rare and heterogeneous mesenchymal tumors, which respond poorly to available systemic treatments. Translation of preclinical findings into clinical applications has been slow, limiting improvements in patients’ outcomes and ultimately highlighting the need for a better understanding of sarcoma biology to develop more effective, subtype-specific therapies. To this end, reliable preclinical models are crucial, but the development of 3D in vitro sarcoma models has been lagging behind that of epithelial cancers. This is primarily due to the rarity and heterogeneity of sarcomas, and lack of widespread knowledge regarding the optimal growth conditions of these in vitro models. In this review, we provide an overview of currently available sarcoma tumoroid models, together with guidelines and suggestions for model development and characterization, on behalf of the FORTRESS (Forum For Translational Research in Sarcomas) international research working group on 3D sarcoma models.
KW - Animals
KW - Cell Culture Techniques, Three Dimensional/methods
KW - Cell Culture Techniques/methods
KW - Humans
KW - Models, Biological
KW - Sarcoma/pathology
UR - https://www.scopus.com/pages/publications/105003981307
UR - https://www.mendeley.com/catalogue/7e8b5494-4345-31aa-b053-44ef440ba36f/
U2 - 10.1016/j.neo.2025.101171
DO - 10.1016/j.neo.2025.101171
M3 - Review article
C2 - 40324303
AN - SCOPUS:105003981307
SN - 1522-8002
VL - 65
SP - 101171
JO - Neoplasia (United States)
JF - Neoplasia (United States)
M1 - 101171
ER -