Large oncosomes in human prostate cancer tissues and in the circulation of mice with metastatic disease

Dolores Di Vizio, Matteo Morello, Andrew C. Dudley, Peter W. Schow, Rosalyn M. Adam, Samantha Morley, David Mulholland, Mirja Rotinen, Martin H. Hager, Luigi Insabato, Marsha A. Moses, Francesca Demichelis, Michael P. Lisanti, Hong Wu, Michael Klagsbrun, Neil A. Bhowmick, Mark A. Rubin, Crislyn D'Souza-Schorey, Michael R. Freeman

Research output: Contribution to journalArticlepeer-review

290 Scopus citations


Oncosomes are tumor-derived microvesicles that transmit signaling complexes between cell and tissue compartments. Herein, we show that amoeboid tumor cells export large (1- to 10-μm diameter) vesicles, derived from bulky cellular protrusions, that contain metalloproteinases, RNA, caveolin-1, and the GTPase ADP-ribosylation factor 6, and are biologically active toward tumor cells, endothelial cells, and fibroblasts. We describe methods by which large oncosomes can be selectively sorted by flow cytometry and analyzed independently of vesicles <1 μm. Structures resembling large oncosomes were identified in the circulation of different mouse models of prostate cancer, and their abundance correlated with tumor progression. Similar large vesicles were also identified in human tumor tissues, but they were not detected in the benign compartment. They were more abundant in metastases. Our results suggest that tumor microvesicles substantially larger than exosome-sized particles can be visualized and quantified in tissues and in the circulation, and isolated and characterized using clinically adaptable methods. These findings also suggest a mechanism by which migrating tumor cells condition the tumor microenvironment and distant sites, thereby potentiating advanced disease.

Original languageEnglish
Pages (from-to)1573-1584
Number of pages12
JournalAmerican Journal of Pathology
Issue number5
StatePublished - Nov 2012
Externally publishedYes


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