Proteomic analysis of ascitic extracellular vesicles describes tumour microenvironment and predicts patient survival in ovarian cancer

Author:

Vyhlídalová Kotrbová Anna1,Gömöryová Kristína1,Mikulová Antónia1,Plešingerová Hana1,Sladeček Stanislava1,Kravec Marek1,Hrachovinová Šárka1ORCID,Potěšil David2,Dunsmore Garett3,Blériot Camille34,Bied Mathilde3,Kotouček Jan5,Bednaříková Markéta6,Hausnerová Jitka7,Minář Luboš8,Crha Igor9,Felsinger Michal8,Zdráhal Zbyněk2,Ginhoux Florent3,Weinberger Vít8,Bryja Vitězslav1,Pospíchalová Vendula1ORCID

Affiliation:

1. Department of Experimental Biology, Faculty of Science Masaryk University Brno Czech Republic

2. Central European Institute of Technology Masaryk University Brno Czech Republic

3. Institut Gustave Roussy, INSERM U1015 Villejuif France

4. Institut Necker Enfants Malades, IMMEDIAB Paris France

5. Department of Pharmacology and Toxicology Veterinary Research Institute Brno Czech Republic

6. Department of Internal Medicine ‐ Hematology & Oncology, University Hospital Brno and Medical Faculty Masaryk University Brno Czech Republic

7. Department of Pathology, University Hospital Brno and Medical Faculty Masaryk University Brno Czech Republic

8. Department of Obstetrics and Gynecology, University Hospital Brno and Medical Faculty Masaryk University Brno Czech Republic

9. Department of Health Sciences, Faculty of Medicine Masaryk University Brno Czech Republic

Abstract

AbstractHigh‐grade serous carcinoma of the ovary, fallopian tube and peritoneum (HGSC), the most common type of ovarian cancer, ranks among the deadliest malignancies. Many HGSC patients have excess fluid in the peritoneum called ascites. Ascites is a tumour microenvironment (TME) containing various cells, proteins and extracellular vesicles (EVs). We isolated EVs from patients’ ascites by orthogonal methods and analyzed them by mass spectrometry. We identified not only a set of ‘core ascitic EV‐associated proteins’ but also defined their subset unique to HGSC ascites. Using single‐cell RNA sequencing data, we mapped the origin of HGSC‐specific EVs to different types of cells present in ascites. Surprisingly, EVs did not come predominantly from tumour cells but from non‐malignant cell types such as macrophages and fibroblasts. Flow cytometry of ascitic cells in combination with analysis of EV protein composition in matched samples showed that analysis of cell type‐specific EV markers in HGSC has more substantial prognostic potential than analysis of ascitic cells. To conclude, we provide evidence that proteomic analysis of EVs can define the cellular composition of HGSC TME. This finding opens numerous avenues both for a better understanding of EV's role in tumour promotion/prevention and for improved HGSC diagnostics.

Funder

Ministerstvo Zdravotnictví Ceské Republiky

Publisher

Wiley

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