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miR-431-5p alters the epithelial-to-mesenchymal transition markers by targeting UROC28 in hepatoma cells
OBJECTIVE: MicroRNA (miR)-431 plays an essential role in various human cancer types, particularly in the process of invasion. However, the function and mechanism of miR-431-5p in the invasion of hepatocellular carcinoma (HCC) remain undefined. METHODS: The expression levels of miR-431-5p and its pot...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177384/ https://www.ncbi.nlm.nih.gov/pubmed/30323624 http://dx.doi.org/10.2147/OTT.S173840 |
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author | Kong, Qinglei Han, Jianhua Deng, Hong Wu, Feilong Guo, Shaozhong Ye, Zhiqiang |
author_facet | Kong, Qinglei Han, Jianhua Deng, Hong Wu, Feilong Guo, Shaozhong Ye, Zhiqiang |
author_sort | Kong, Qinglei |
collection | PubMed |
description | OBJECTIVE: MicroRNA (miR)-431 plays an essential role in various human cancer types, particularly in the process of invasion. However, the function and mechanism of miR-431-5p in the invasion of hepatocellular carcinoma (HCC) remain undefined. METHODS: The expression levels of miR-431-5p and its potential target protein UROC28 in hepatocellular carcinoma cells and tissues were detected, and the levels of EMT markers in vivo and in vitro were also detected. RESULTS: MiR-431-5p was downregulated in HCC cell lines and tissues and associated with vascular invasion and tumor encapsulation. Furthermore, miR-431-5p was able to influence the epithelialto-mesenchymal transition (EMT) process in HCCLM3 and HUH7 cells. Mechanistically, it was discovered that miR-431-5p repressed invasion by targeting UROC28. Furthermore, miR-431-5p influenced the EMT markers in HCCLM3 and HUH7 cells by downregulating UROC28 expression. Similarly, in vivo assays confirmed that miR-431-5p upregulation in HCC cells remarkably inhibited tumor proliferation and influenced the EMT markers. CONCLUSION: The current study has demonstrated that the miR-431-5p/UROC28 axis acts possible influence on the EMT in HCC. Upregulation of miR-431-5p could be an original approach for inhibiting tumor invasion. |
format | Online Article Text |
id | pubmed-6177384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61773842018-10-15 miR-431-5p alters the epithelial-to-mesenchymal transition markers by targeting UROC28 in hepatoma cells Kong, Qinglei Han, Jianhua Deng, Hong Wu, Feilong Guo, Shaozhong Ye, Zhiqiang Onco Targets Ther Original Research OBJECTIVE: MicroRNA (miR)-431 plays an essential role in various human cancer types, particularly in the process of invasion. However, the function and mechanism of miR-431-5p in the invasion of hepatocellular carcinoma (HCC) remain undefined. METHODS: The expression levels of miR-431-5p and its potential target protein UROC28 in hepatocellular carcinoma cells and tissues were detected, and the levels of EMT markers in vivo and in vitro were also detected. RESULTS: MiR-431-5p was downregulated in HCC cell lines and tissues and associated with vascular invasion and tumor encapsulation. Furthermore, miR-431-5p was able to influence the epithelialto-mesenchymal transition (EMT) process in HCCLM3 and HUH7 cells. Mechanistically, it was discovered that miR-431-5p repressed invasion by targeting UROC28. Furthermore, miR-431-5p influenced the EMT markers in HCCLM3 and HUH7 cells by downregulating UROC28 expression. Similarly, in vivo assays confirmed that miR-431-5p upregulation in HCC cells remarkably inhibited tumor proliferation and influenced the EMT markers. CONCLUSION: The current study has demonstrated that the miR-431-5p/UROC28 axis acts possible influence on the EMT in HCC. Upregulation of miR-431-5p could be an original approach for inhibiting tumor invasion. Dove Medical Press 2018-10-04 /pmc/articles/PMC6177384/ /pubmed/30323624 http://dx.doi.org/10.2147/OTT.S173840 Text en © 2018 Kong et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Kong, Qinglei Han, Jianhua Deng, Hong Wu, Feilong Guo, Shaozhong Ye, Zhiqiang miR-431-5p alters the epithelial-to-mesenchymal transition markers by targeting UROC28 in hepatoma cells |
title | miR-431-5p alters the epithelial-to-mesenchymal transition markers by targeting UROC28 in hepatoma cells |
title_full | miR-431-5p alters the epithelial-to-mesenchymal transition markers by targeting UROC28 in hepatoma cells |
title_fullStr | miR-431-5p alters the epithelial-to-mesenchymal transition markers by targeting UROC28 in hepatoma cells |
title_full_unstemmed | miR-431-5p alters the epithelial-to-mesenchymal transition markers by targeting UROC28 in hepatoma cells |
title_short | miR-431-5p alters the epithelial-to-mesenchymal transition markers by targeting UROC28 in hepatoma cells |
title_sort | mir-431-5p alters the epithelial-to-mesenchymal transition markers by targeting uroc28 in hepatoma cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177384/ https://www.ncbi.nlm.nih.gov/pubmed/30323624 http://dx.doi.org/10.2147/OTT.S173840 |
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