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Heterotypic CAF-tumor spheroids promote early peritoneal metastatis of ovarian cancer

High-grade serous ovarian cancer (HGSOC) is hallmarked by early onset of peritoneal dissemination, which distinguishes it from low-grade serous ovarian cancer (LGSOC). Here, we describe the aggressive nature of HGSOC ascitic tumor cells (ATCs) characterized by integrin α5(high) (ITGA5(high)) ATCs, w...

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Detalles Bibliográficos
Autores principales: Gao, Qinglei, Yang, Zongyuan, Xu, Sen, Li, Xiaoting, Yang, Xin, Jin, Ping, Liu, Yi, Zhou, Xiaoshui, Zhang, Taoran, Gong, Cheng, Wei, Xiao, Liu, Dan, Sun, Chaoyang, Chen, Gang, Hu, Junbo, Meng, Li, Zhou, Jianfeng, Sawada, Kenjiro, Fruscio, Robert, Grunt, Thomas W., Wischhusen, Jörg, Vargas-Hernández, Víctor Manuel, Pothuri, Bhavana, Coleman, Robert L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400537/
https://www.ncbi.nlm.nih.gov/pubmed/30710055
http://dx.doi.org/10.1084/jem.20180765
Descripción
Sumario:High-grade serous ovarian cancer (HGSOC) is hallmarked by early onset of peritoneal dissemination, which distinguishes it from low-grade serous ovarian cancer (LGSOC). Here, we describe the aggressive nature of HGSOC ascitic tumor cells (ATCs) characterized by integrin α5(high) (ITGA5(high)) ATCs, which are prone to forming heterotypic spheroids with fibroblasts. We term these aggregates as metastatic units (MUs) in HGSOC for their advantageous metastatic capacity and active involvement in early peritoneal dissemination. Intriguingly, fibroblasts inside MUs support ATC survival and guide their peritoneal invasion before becoming essential components of the tumor stroma in newly formed metastases. Cancer-associated fibroblasts (CAFs) recruit ITGA5(high) ATCs to form MUs, which further sustain ATC ITGA5 expression by EGF secretion. Notably, LGSOC is largely devoid of CAFs and the resultant MUs, which might explain its metastatic delay. These findings identify a specialized MU architecture that amplifies the tumor–stroma interaction and promotes transcoelomic metastasis in HGSOC, providing the basis for stromal fibroblast-oriented interventions in hampering OC peritoneal propagation.