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Tumor suppressive role of miR-569 in lung cancer

microRNAs (miRs) are targets for genomic aberrations and emerging treatments against cancer. It has been demonstrated that targeting miR-569 may potentially benefit patients with ovarian or breast cancer. However, the exact roles of miR-569 remain unclear in human lung cancer cells. Using the revers...

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Detalles Bibliográficos
Autores principales: Zheng, Yi Ping, Wu, Linxia, Gao, Jie, Wang, Yanfu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835959/
https://www.ncbi.nlm.nih.gov/pubmed/29541173
http://dx.doi.org/10.3892/ol.2018.7869
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author Zheng, Yi Ping
Wu, Linxia
Gao, Jie
Wang, Yanfu
author_facet Zheng, Yi Ping
Wu, Linxia
Gao, Jie
Wang, Yanfu
author_sort Zheng, Yi Ping
collection PubMed
description microRNAs (miRs) are targets for genomic aberrations and emerging treatments against cancer. It has been demonstrated that targeting miR-569 may potentially benefit patients with ovarian or breast cancer. However, the exact roles of miR-569 remain unclear in human lung cancer cells. Using the reverse transcription-quantitative polymerase chain reaction (RT-qPCR), it was demonstrated that miR-569 expression was consistently decreased in lung cancer cells. As well as cell proliferation and migration inhibition, apoptosis and cell arrest at the G1 phase were induced following reversion of miR-569 expression in lung cancer cells. The present study demonstrated that miR-569 was able to downregulate FOS and high mobility group A2 mRNA and protein expression using RT-qPCR and western blot analysis. The observed role of miRNA-569 in lung cancer cells in the present study suggested that it may be a novel and promising therapeutic target, and a novel biomarker for detecting lung cancer.
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spelling pubmed-58359592018-03-14 Tumor suppressive role of miR-569 in lung cancer Zheng, Yi Ping Wu, Linxia Gao, Jie Wang, Yanfu Oncol Lett Articles microRNAs (miRs) are targets for genomic aberrations and emerging treatments against cancer. It has been demonstrated that targeting miR-569 may potentially benefit patients with ovarian or breast cancer. However, the exact roles of miR-569 remain unclear in human lung cancer cells. Using the reverse transcription-quantitative polymerase chain reaction (RT-qPCR), it was demonstrated that miR-569 expression was consistently decreased in lung cancer cells. As well as cell proliferation and migration inhibition, apoptosis and cell arrest at the G1 phase were induced following reversion of miR-569 expression in lung cancer cells. The present study demonstrated that miR-569 was able to downregulate FOS and high mobility group A2 mRNA and protein expression using RT-qPCR and western blot analysis. The observed role of miRNA-569 in lung cancer cells in the present study suggested that it may be a novel and promising therapeutic target, and a novel biomarker for detecting lung cancer. D.A. Spandidos 2018-04 2018-01-26 /pmc/articles/PMC5835959/ /pubmed/29541173 http://dx.doi.org/10.3892/ol.2018.7869 Text en Copyright: © Zheng et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Zheng, Yi Ping
Wu, Linxia
Gao, Jie
Wang, Yanfu
Tumor suppressive role of miR-569 in lung cancer
title Tumor suppressive role of miR-569 in lung cancer
title_full Tumor suppressive role of miR-569 in lung cancer
title_fullStr Tumor suppressive role of miR-569 in lung cancer
title_full_unstemmed Tumor suppressive role of miR-569 in lung cancer
title_short Tumor suppressive role of miR-569 in lung cancer
title_sort tumor suppressive role of mir-569 in lung cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835959/
https://www.ncbi.nlm.nih.gov/pubmed/29541173
http://dx.doi.org/10.3892/ol.2018.7869
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