Your browser doesn't support javascript.
loading
miR-26a regulates extracellular vesicle secretion from prostate cancer cells via targeting SHC4, PFDN4, and CHORDC1.
Urabe, Fumihiko; Kosaka, Nobuyoshi; Sawa, Yurika; Yamamoto, Yusuke; Ito, Kagenori; Yamamoto, Tomofumi; Kimura, Takahiro; Egawa, Shin; Ochiya, Takahiro.
Afiliação
  • Urabe F; Department of Molecular and Cellular Medicine, Institute of Medical Science, Tokyo Medical University, Tokyo, Japan.
  • Kosaka N; Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.
  • Sawa Y; Division of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
  • Yamamoto Y; Department of Molecular and Cellular Medicine, Institute of Medical Science, Tokyo Medical University, Tokyo, Japan.
  • Ito K; Department of Molecular and Cellular Medicine, Institute of Medical Science, Tokyo Medical University, Tokyo, Japan.
  • Yamamoto T; Division of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
  • Kimura T; Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.
  • Egawa S; Division of Cellular Signaling, National Cancer Center Research Institute, Tokyo, Japan.
  • Ochiya T; Department of Molecular and Cellular Medicine, Institute of Medical Science, Tokyo Medical University, Tokyo, Japan.
Sci Adv ; 6(18): eaay3051, 2020 05.
Article em En | MEDLINE | ID: mdl-32494663
ABSTRACT
Extracellular vesicles (EVs) are involved in intercellular communication during cancer progression; thus, elucidating the mechanism of EV secretion in cancer cells will contribute to the development of an EV-targeted cancer treatment. However, the biogenesis of EVs in cancer cells is not fully understood. MicroRNAs (miRNAs) regulate a variety of biological phenomena; thus, miRNAs could regulate EV secretion. Here, we performed high-throughput miRNA-based screening to identify the regulators of EV secretion using an ExoScreen assay. By using this method, we identified miR-26a involved in EV secretion from prostate cancer (PCa) cells. In addition, we found that SHC4, PFDN4, and CHORDC1 genes regulate EV secretion in PCa cells. Furthermore, the progression of the PCa cells suppressing these genes was inhibited in an in vivo study. Together, our findings suggest that miR-26a regulates EV secretion via targeting SHC4, PFDN4, and CHORDC1 in PCa cells, resulting in the suppression of PCa progression.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / MicroRNAs / Vesículas Extracelulares Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / MicroRNAs / Vesículas Extracelulares Idioma: En Ano de publicação: 2020 Tipo de documento: Article