Prostate carcinoma (PCa) progression is strongly influenced by the surrounding tumor microenvironment, where cancer-associated fibroblasts (CAFs) represent the most abundant and functionally relevant stromal population. Despite their importance, the lack of stable cell lines representing CAF phenotypes limits the study of stromal–tumor interactions. To address this limitation, we provide an optimized protocol for isolating CAFs from fresh human PCa biopsies based on a mechanical procedure exploiting the specific CAF ability to migrate out from the tumor explants. This approach preserves tissue architecture and maintains CAF viability and phenotype. The resulting ex vivo CAF cultures provide a suitable model to investigate CAF biology within the tumor microenvironment.

Non-Enzymatic Isolation of Cancer-Associated Fibroblasts From Human Prostate Tumor Explants / Gangarossa, G., Grillo, C., Roccabianca, S., Pranzini, E., Iozzo, M., Venditti, G., Bertoli, G., Ippolito, L., Giannoni, E., Comito, G., Chiarugi, P.. - In: BIO-PROTOCOL. - ISSN 2331-8325. - ELETTRONICO. - 16:(2026), pp. e5614.0-e5614.0. [10.21769/bioprotoc.5614]

Non-Enzymatic Isolation of Cancer-Associated Fibroblasts From Human Prostate Tumor Explants

Gangarossa, Giulia;Grillo, Caterina;Roccabianca, Sara;Pranzini, Erica;Iozzo, Marta;Venditti, Giacomo;Bertoli, Greta;Ippolito, Luigi
;
Giannoni, Elisa;Comito, Giuseppina;Chiarugi, Paola
2026

Abstract

Prostate carcinoma (PCa) progression is strongly influenced by the surrounding tumor microenvironment, where cancer-associated fibroblasts (CAFs) represent the most abundant and functionally relevant stromal population. Despite their importance, the lack of stable cell lines representing CAF phenotypes limits the study of stromal–tumor interactions. To address this limitation, we provide an optimized protocol for isolating CAFs from fresh human PCa biopsies based on a mechanical procedure exploiting the specific CAF ability to migrate out from the tumor explants. This approach preserves tissue architecture and maintains CAF viability and phenotype. The resulting ex vivo CAF cultures provide a suitable model to investigate CAF biology within the tumor microenvironment.
2026
16
0
0
Gangarossa, Giulia; Grillo, Caterina; Roccabianca, Sara; Pranzini, Erica; Iozzo, Marta; Venditti, Giacomo; Bertoli, Greta; Ippolito, Luigi; Giannoni, ...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1491592
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