Endothelium and subendothelial matrix mechanics modulate cancer cell transendothelial migration

Cancer cell extravasation, a key step in the metastatic cascade, involves cancer cell arrest on the endothelium, transendothelial migration (TEM), followed by the invasion into the subendothelial extracellular matrix (ECM) of distant tissues. While cancer research has mostly focused on the biomechan...

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Detalles Bibliográficos
Autores: Javanmardi, Yousef, Agrawal, Ayushi, Malandrino, Andrea, Lasli, Soufian, Chen, Michelle, Shahreza, Somayeh, Serwinski, Bianca, Cammoun, Leila, Li, Ran, Jorfi, Mehdi, Djordjevic, Boris, Szita, Nicolas, Spill, Fabian, Bertazzo, Sergio, Sheridan, Graham K, Shenoy, Vivek, Calvo González, Fernando|||0000-0001-8858-1185, Kamm, Roger, Moeendarbary, Emad
Tipo de recurso: artículo
Fecha de publicación:2023
País:España
Institución:Universidad de Cantabria (UC)
Repositorio:UCrea Repositorio Abierto de la Universidad de Cantabria
Idioma:inglés
OAI Identifier:oai:repositorio.unican.es:10902/30083
Acceso en línea:https://hdl.handle.net/10902/30083
Access Level:acceso abierto
Palabra clave:Biomaterial properties
Cancer cell extravasation
Computational modeling
Metastasis
Traction force microscopy
Descripción
Sumario:Cancer cell extravasation, a key step in the metastatic cascade, involves cancer cell arrest on the endothelium, transendothelial migration (TEM), followed by the invasion into the subendothelial extracellular matrix (ECM) of distant tissues. While cancer research has mostly focused on the biomechanical interactions between tumor cells (TCs) and ECM, particularly at the primary tumor site, very little is known about the mechanical properties of endothelial cells and the subendothelial ECM and how they contribute to the extravasation process. Here, an integrated experimental and theoretical framework is developed to investigate the mechanical crosstalk between TCs, endothelium and subendothelial ECM during in vitro cancer cell extravasation. It is found that cancer cell actin-rich protrusions generate complex push-pull forces to initiate and drive TEM, while transmigration success also relies on the forces generated by the endothelium. Consequently, mechanical properties of the subendothelial ECM and endothelial actomyosin contractility that mediate the endothelial forces also impact the endothelium's resistance to cancer cell transmigration. These results indicate that mechanical features of distant tissues, including force interactions between the endothelium and the subendothelial ECM, are key determinants of metastatic organotropism