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

Author:

Gao Qinglei1ORCID,Yang Zongyuan1,Xu Sen1,Li Xiaoting1,Yang Xin1,Jin Ping1,Liu Yi1,Zhou Xiaoshui1,Zhang Taoran1,Gong Cheng1,Wei Xiao1,Liu Dan1,Sun Chaoyang1,Chen Gang1,Hu Junbo1,Meng Li2,Zhou Jianfeng2,Sawada Kenjiro3,Fruscio Robert45ORCID,Grunt Thomas W.6,Wischhusen Jörg7,Vargas-Hernández Víctor Manuel8ORCID,Pothuri Bhavana9,Coleman Robert L.10

Affiliation:

1. Cancer Biology Research Center (Key Laboratory of the Ministry of Education), Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China

2. Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China

3. Department of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, Yamadaoka Suita, Osaka, Japan

4. Clinic of Obstetrics and Gynecology, San Gerardo Hospital, Monza, Italy

5. Department of Medicine and Surgery, University of Milan-Bicocca, Milan, Italy

6. Signaling Networks Program, Division of Oncology, Department of Medicine I, Comprehensive Cancer Center & Ludwig Boltzmann Cluster Oncology, Medical University of Vienna, Vienna, Austria

7. Department of Obstetrics and Gynecology, Experimental Tumor Immunology, University of Würzburg Medical School, Würzburg, Germany

8. Dirección de Investigación, Hospital Juárez de México D.F., Nápoles, Mexico City, Mexico

9. Division of Gynecological Oncology, NYU Langone Medical Center, Perlmutter Cancer Center, New York, NY

10. Department of Gynecological Oncology & Reproductive Medicine, University of Texas, M.D. Anderson Cancer Center, Houston, TX

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.

Funder

National Science Foundation of China

“973” Program of China

National Key Research & Development Program of China

National Science and Technology Major Sub-Project

Technical Innovation Special Project of Hubei Province

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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