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Alterations in exosomal miRNA profile upon epithelial-mesenchymal transition in human lung cancer cell lines
BACKGROUND: Epithelial–mesenchymal transition (EMT) is regarded as a critical event during tumor metastasis. Recent studies have revealed changes and the contributions of proteins in/on exosomes during EMT. Besides proteins, microRNA (miRNA) is another important functional component of exosomes. We...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219194/ https://www.ncbi.nlm.nih.gov/pubmed/30400814 http://dx.doi.org/10.1186/s12864-018-5143-6 |
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author | Tang, Yue-Ting Huang, Yi-Yao Li, Jing-Huan Qin, Si-Hua Xu, Yong An, Tai-Xue Liu, Chun-Chen Wang, Qian Zheng, Lei |
author_facet | Tang, Yue-Ting Huang, Yi-Yao Li, Jing-Huan Qin, Si-Hua Xu, Yong An, Tai-Xue Liu, Chun-Chen Wang, Qian Zheng, Lei |
author_sort | Tang, Yue-Ting |
collection | PubMed |
description | BACKGROUND: Epithelial–mesenchymal transition (EMT) is regarded as a critical event during tumor metastasis. Recent studies have revealed changes and the contributions of proteins in/on exosomes during EMT. Besides proteins, microRNA (miRNA) is another important functional component of exosomes. We hypothesized that the miRNA profile of exosomes may change following EMT and these exosomal miRNAs may in return promote EMT, migration and invasion of cancer cells. RESULTS: The small RNA profile of exosomes was altered following EMT. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis revealed that the specific miRNAs of M-exosomes have the potential to drive signal transduction networks in EMT and cancer progression. Co-culture experiments confirmed that M-exosomes can enter epithelial cells and promote migration, invasion and expression of mesenchymal markers in the recipient cells. CONCLUSION: Our results reveal changes in the function and miRNA profile of exosomes upon EMT. M-exosomes can promote transfer of the malignant (mesenchymal) phenotype to epithelial recipient cells. Further, the miRNAs specifically expressed in M-exosomes are associated with EMT and metastasis, and may serve as new biomarkers for EMT-like processes in lung cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5143-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6219194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62191942018-11-16 Alterations in exosomal miRNA profile upon epithelial-mesenchymal transition in human lung cancer cell lines Tang, Yue-Ting Huang, Yi-Yao Li, Jing-Huan Qin, Si-Hua Xu, Yong An, Tai-Xue Liu, Chun-Chen Wang, Qian Zheng, Lei BMC Genomics Research Article BACKGROUND: Epithelial–mesenchymal transition (EMT) is regarded as a critical event during tumor metastasis. Recent studies have revealed changes and the contributions of proteins in/on exosomes during EMT. Besides proteins, microRNA (miRNA) is another important functional component of exosomes. We hypothesized that the miRNA profile of exosomes may change following EMT and these exosomal miRNAs may in return promote EMT, migration and invasion of cancer cells. RESULTS: The small RNA profile of exosomes was altered following EMT. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis revealed that the specific miRNAs of M-exosomes have the potential to drive signal transduction networks in EMT and cancer progression. Co-culture experiments confirmed that M-exosomes can enter epithelial cells and promote migration, invasion and expression of mesenchymal markers in the recipient cells. CONCLUSION: Our results reveal changes in the function and miRNA profile of exosomes upon EMT. M-exosomes can promote transfer of the malignant (mesenchymal) phenotype to epithelial recipient cells. Further, the miRNAs specifically expressed in M-exosomes are associated with EMT and metastasis, and may serve as new biomarkers for EMT-like processes in lung cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5143-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-06 /pmc/articles/PMC6219194/ /pubmed/30400814 http://dx.doi.org/10.1186/s12864-018-5143-6 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Tang, Yue-Ting Huang, Yi-Yao Li, Jing-Huan Qin, Si-Hua Xu, Yong An, Tai-Xue Liu, Chun-Chen Wang, Qian Zheng, Lei Alterations in exosomal miRNA profile upon epithelial-mesenchymal transition in human lung cancer cell lines |
title | Alterations in exosomal miRNA profile upon epithelial-mesenchymal transition in human lung cancer cell lines |
title_full | Alterations in exosomal miRNA profile upon epithelial-mesenchymal transition in human lung cancer cell lines |
title_fullStr | Alterations in exosomal miRNA profile upon epithelial-mesenchymal transition in human lung cancer cell lines |
title_full_unstemmed | Alterations in exosomal miRNA profile upon epithelial-mesenchymal transition in human lung cancer cell lines |
title_short | Alterations in exosomal miRNA profile upon epithelial-mesenchymal transition in human lung cancer cell lines |
title_sort | alterations in exosomal mirna profile upon epithelial-mesenchymal transition in human lung cancer cell lines |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219194/ https://www.ncbi.nlm.nih.gov/pubmed/30400814 http://dx.doi.org/10.1186/s12864-018-5143-6 |
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