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Extracellular RNA transfer from non‐malignant human cholangiocytes can promote cholangiocarcinoma growth
Extracellular vesicles (EV) within the cellular secretome are emerging as modulators of pathological processes involved in tumor growth through their ability to transfer donor‐derived RNA into recipient cells. While the effects of tumor and stromal cell EVs within the tumor microenvironment have bee...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634862/ https://www.ncbi.nlm.nih.gov/pubmed/34510808 http://dx.doi.org/10.1002/2211-5463.13294 |
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author | Ota, Yu Takahashi, Kenji Otake, Shin Tamaki, Yosui Okada, Mitsuyoshi Yan, Irene Aso, Kazunobu Fujii, Satoshi Patel, Tushar Haneda, Masakazu |
author_facet | Ota, Yu Takahashi, Kenji Otake, Shin Tamaki, Yosui Okada, Mitsuyoshi Yan, Irene Aso, Kazunobu Fujii, Satoshi Patel, Tushar Haneda, Masakazu |
author_sort | Ota, Yu |
collection | PubMed |
description | Extracellular vesicles (EV) within the cellular secretome are emerging as modulators of pathological processes involved in tumor growth through their ability to transfer donor‐derived RNA into recipient cells. While the effects of tumor and stromal cell EVs within the tumor microenvironment have been studied, less is known about the contributions of normal, nontransformed cells. We examined the impact of EVs within the cellular secretome from nonmalignant cells on transformed cell growth and behavior in cholangiocarcinoma cells. These effects were enhanced in the presence of the pro‐fibrogenic mediator TGF‐β. We identified miR‐195 as a TGF‐β responsive miRNA in normal cells that can be transferred via EV to tumor cells and regulate cell growth, invasion, and migration. The effects of miR‐195 involve modulation of the epithelial–mesenchymal transition through direct effects on the transcription factor Snail. These studies provide in vitro and in vivo evidence for the impact of normal cellular secretome on transformed cell growth, show the importance of EV RNA transfer, and identify mechanisms of EV‐mediated transfer of miRNA as a contributor to tumor development, which may provide new therapeutic opportunities for targeting human cholangiocarcinoma. |
format | Online Article Text |
id | pubmed-8634862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86348622021-12-08 Extracellular RNA transfer from non‐malignant human cholangiocytes can promote cholangiocarcinoma growth Ota, Yu Takahashi, Kenji Otake, Shin Tamaki, Yosui Okada, Mitsuyoshi Yan, Irene Aso, Kazunobu Fujii, Satoshi Patel, Tushar Haneda, Masakazu FEBS Open Bio Research Articles Extracellular vesicles (EV) within the cellular secretome are emerging as modulators of pathological processes involved in tumor growth through their ability to transfer donor‐derived RNA into recipient cells. While the effects of tumor and stromal cell EVs within the tumor microenvironment have been studied, less is known about the contributions of normal, nontransformed cells. We examined the impact of EVs within the cellular secretome from nonmalignant cells on transformed cell growth and behavior in cholangiocarcinoma cells. These effects were enhanced in the presence of the pro‐fibrogenic mediator TGF‐β. We identified miR‐195 as a TGF‐β responsive miRNA in normal cells that can be transferred via EV to tumor cells and regulate cell growth, invasion, and migration. The effects of miR‐195 involve modulation of the epithelial–mesenchymal transition through direct effects on the transcription factor Snail. These studies provide in vitro and in vivo evidence for the impact of normal cellular secretome on transformed cell growth, show the importance of EV RNA transfer, and identify mechanisms of EV‐mediated transfer of miRNA as a contributor to tumor development, which may provide new therapeutic opportunities for targeting human cholangiocarcinoma. John Wiley and Sons Inc. 2021-09-22 /pmc/articles/PMC8634862/ /pubmed/34510808 http://dx.doi.org/10.1002/2211-5463.13294 Text en © 2021 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Ota, Yu Takahashi, Kenji Otake, Shin Tamaki, Yosui Okada, Mitsuyoshi Yan, Irene Aso, Kazunobu Fujii, Satoshi Patel, Tushar Haneda, Masakazu Extracellular RNA transfer from non‐malignant human cholangiocytes can promote cholangiocarcinoma growth |
title | Extracellular RNA transfer from non‐malignant human cholangiocytes can promote cholangiocarcinoma growth |
title_full | Extracellular RNA transfer from non‐malignant human cholangiocytes can promote cholangiocarcinoma growth |
title_fullStr | Extracellular RNA transfer from non‐malignant human cholangiocytes can promote cholangiocarcinoma growth |
title_full_unstemmed | Extracellular RNA transfer from non‐malignant human cholangiocytes can promote cholangiocarcinoma growth |
title_short | Extracellular RNA transfer from non‐malignant human cholangiocytes can promote cholangiocarcinoma growth |
title_sort | extracellular rna transfer from non‐malignant human cholangiocytes can promote cholangiocarcinoma growth |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634862/ https://www.ncbi.nlm.nih.gov/pubmed/34510808 http://dx.doi.org/10.1002/2211-5463.13294 |
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