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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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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. |
format | Online Article Text |
id | pubmed-7190312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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