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miR-26a regulates extracellular vesicle secretion from prostate cancer cells via targeting SHC4, PFDN4, and CHORDC1

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 under...

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Autores principales: Urabe, Fumihiko, Kosaka, Nobuyoshi, Sawa, Yurika, Yamamoto, Yusuke, Ito, Kagenori, Yamamoto, Tomofumi, Kimura, Takahiro, Egawa, Shin, Ochiya, Takahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190312/
https://www.ncbi.nlm.nih.gov/pubmed/32494663
http://dx.doi.org/10.1126/sciadv.aay3051
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author Urabe, Fumihiko
Kosaka, Nobuyoshi
Sawa, Yurika
Yamamoto, Yusuke
Ito, Kagenori
Yamamoto, Tomofumi
Kimura, Takahiro
Egawa, Shin
Ochiya, Takahiro
author_facet Urabe, Fumihiko
Kosaka, Nobuyoshi
Sawa, Yurika
Yamamoto, Yusuke
Ito, Kagenori
Yamamoto, Tomofumi
Kimura, Takahiro
Egawa, Shin
Ochiya, Takahiro
author_sort Urabe, Fumihiko
collection PubMed
description 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.
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spelling pubmed-71903122020-06-02 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 Sci Adv Research Articles 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. American Association for the Advancement of Science 2020-04-29 /pmc/articles/PMC7190312/ /pubmed/32494663 http://dx.doi.org/10.1126/sciadv.aay3051 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Urabe, Fumihiko
Kosaka, Nobuyoshi
Sawa, Yurika
Yamamoto, Yusuke
Ito, Kagenori
Yamamoto, Tomofumi
Kimura, Takahiro
Egawa, Shin
Ochiya, Takahiro
miR-26a regulates extracellular vesicle secretion from prostate cancer cells via targeting SHC4, PFDN4, and CHORDC1
title miR-26a regulates extracellular vesicle secretion from prostate cancer cells via targeting SHC4, PFDN4, and CHORDC1
title_full miR-26a regulates extracellular vesicle secretion from prostate cancer cells via targeting SHC4, PFDN4, and CHORDC1
title_fullStr miR-26a regulates extracellular vesicle secretion from prostate cancer cells via targeting SHC4, PFDN4, and CHORDC1
title_full_unstemmed miR-26a regulates extracellular vesicle secretion from prostate cancer cells via targeting SHC4, PFDN4, and CHORDC1
title_short miR-26a regulates extracellular vesicle secretion from prostate cancer cells via targeting SHC4, PFDN4, and CHORDC1
title_sort mir-26a regulates extracellular vesicle secretion from prostate cancer cells via targeting shc4, pfdn4, and chordc1
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190312/
https://www.ncbi.nlm.nih.gov/pubmed/32494663
http://dx.doi.org/10.1126/sciadv.aay3051
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