Metastatic prostate cancer‐derived extracellular vesicles facilitate osteoclastogenesis by transferring the CDCP1 protein

Author:

Urabe Fumihiko12ORCID,Kosaka Nobuyoshi3,Yamamoto Yusuke2,Ito Kagenori12,Otsuka Kurataka234,Soekmadji Carolina5ORCID,Egawa Shin1,Kimura Takahiro1,Ochiya Takahiro3ORCID

Affiliation:

1. Department of Urology The Jikei University School of Medicine Tokyo Japan

2. Laboratory of Integrative Oncology National Cancer Center Research Institute Tokyo Japan

3. Department of Molecular and Cellular Medicine Institute of Medical Science, Tokyo Medical University Tokyo Japan

4. R&D Division, Kewpie Corporation Sengawa Kewport Tokyo Japan

5. School of Biomedical Sciences, Faculty of Medicine University of Queensland Brisbane Australia

Abstract

AbstractBone metastases are still incurable and result in the development of clinical complications and decreased survival for prostate cancer patients. Recently, a number of studies have shown that extracellular vesicles (EVs) play important roles in tumour progression. Here, we show that EVs from metastatic prostate cancer cells promote osteoclast formation in the presence of receptor activator of NF‐κB ligand (RANKL). EV characterization followed by functional siRNA screening identified CUB‐domain containing protein 1 (CDCP1), a transmembrane protein, as an inducer of osteoclastogenesis. Additionally, CDCP1 expression on plasma‐derived EVs was upregulated in bone metastatic prostate cancer patients. Our findings elucidate the effect of EVs from metastatic prostate cancer cells on osteoclast formation, which is promoted by CDCP1 located on EVs. Furthermore, our data suggested that CDCP1 expression on EVs might be useful to detect bone metastasis of prostate cancer.

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Japanese Urological Association

Japanese Foundation for Prostate Research

U.S. Department of Defense

Publisher

Wiley

Subject

Cell Biology,Histology

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