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

Qinglei Gao(Tongji Hospital), Zongyuan Yang(Tongji Hospital), Sen Xu(Tongji Hospital), Xiaoting Li(Tongji Hospital), Xin Yang(Tongji Hospital), Ping Jin(Tongji Hospital), Yi Liu(Tongji Hospital), Xiaoshui Zhou(Tongji Hospital), Taoran Zhang(Tongji Hospital), Cheng Gong(Tongji Hospital), Wei Xiao(Tongji Hospital), Dan Liu(Tongji Hospital), Chaoyang Sun(Tongji Hospital), Gang Chen(Tongji Hospital), Junbo Hu(Tongji Hospital), Meng Li(Tongji Hospital), Jianfeng Zhou(Tongji Hospital), Kenjiro Sawada(The University of Osaka), Robert Fruscio(Azienda Ospedaliera San Gerardo), Thomas W. Grunt(Comprehensive Cancer Center Vienna), Jörg Wischhusen(University of Würzburg), Víctor Manuel Vargas-Hernández(Hospital Juárez de México), Bhavana Pothuri(NYU Langone Health), Robert L. Coleman(The University of Texas MD Anderson Cancer Center)
The Journal of Experimental Medicine
February 1, 2019
Cited by 254Open Access
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Abstract

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 α5high (ITGA5high) 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 ITGA5high 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.


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