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MicroRNA-524 promotes cell proliferation by down-regulating PTEN expression in osteosarcoma

BACKGROUND: Increasing numbers of studies have examined the correlation between specific miRNAs and tumours to enable their diagnosis and treatment. However, there are few reports regarding the concrete role and mechanism of miRNA in osteosarcoma. METHODS: The expression of miR-524 in osteosarcoma t...

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Autores principales: Zhuang, Ming, Qiu, Xubin, Cheng, Dong, Zhu, Chenlei, Chen, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090628/
https://www.ncbi.nlm.nih.gov/pubmed/30123092
http://dx.doi.org/10.1186/s12935-018-0612-1
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author Zhuang, Ming
Qiu, Xubin
Cheng, Dong
Zhu, Chenlei
Chen, Liang
author_facet Zhuang, Ming
Qiu, Xubin
Cheng, Dong
Zhu, Chenlei
Chen, Liang
author_sort Zhuang, Ming
collection PubMed
description BACKGROUND: Increasing numbers of studies have examined the correlation between specific miRNAs and tumours to enable their diagnosis and treatment. However, there are few reports regarding the concrete role and mechanism of miRNA in osteosarcoma. METHODS: The expression of miR-524 in osteosarcoma tissues and cell lines was examined by qRT-PCR. The cell proliferation was examined using CCK-8 in vitro. A series of bioinformatics and molecular biology techniques were adopted to investigate the regulatory relationship between miR-524 and target genes in osteosarcoma. RESULTS: The results showed that the miRNA with the most significant differential expression in osteosarcoma was miR-524, which was significantly up-regulated in both osteosarcoma tissues and cell lines. MiR-524 knockdown inhibited proliferation and promoted apoptosis of osteosarcoma cells, while overexpression of miR-524 induced their proliferation. Bioinformatics analysis and luciferase assay confirmed that PTEN was a direct target gene of miR-524 and that miR-524 induced proliferation of osteosarcoma cells through activation of the PI3K/AKT pathway via inhibition of PTEN. CONCLUSIONS: MiR-524 induces the proliferation of osteosarcoma cells through activation of the PI3K/AKT pathway via inhibition of the target gene PTEN, which provides a theoretical basis for selecting a new therapeutic target for osteosarcoma. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12935-018-0612-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-60906282018-08-17 MicroRNA-524 promotes cell proliferation by down-regulating PTEN expression in osteosarcoma Zhuang, Ming Qiu, Xubin Cheng, Dong Zhu, Chenlei Chen, Liang Cancer Cell Int Primary Research BACKGROUND: Increasing numbers of studies have examined the correlation between specific miRNAs and tumours to enable their diagnosis and treatment. However, there are few reports regarding the concrete role and mechanism of miRNA in osteosarcoma. METHODS: The expression of miR-524 in osteosarcoma tissues and cell lines was examined by qRT-PCR. The cell proliferation was examined using CCK-8 in vitro. A series of bioinformatics and molecular biology techniques were adopted to investigate the regulatory relationship between miR-524 and target genes in osteosarcoma. RESULTS: The results showed that the miRNA with the most significant differential expression in osteosarcoma was miR-524, which was significantly up-regulated in both osteosarcoma tissues and cell lines. MiR-524 knockdown inhibited proliferation and promoted apoptosis of osteosarcoma cells, while overexpression of miR-524 induced their proliferation. Bioinformatics analysis and luciferase assay confirmed that PTEN was a direct target gene of miR-524 and that miR-524 induced proliferation of osteosarcoma cells through activation of the PI3K/AKT pathway via inhibition of PTEN. CONCLUSIONS: MiR-524 induces the proliferation of osteosarcoma cells through activation of the PI3K/AKT pathway via inhibition of the target gene PTEN, which provides a theoretical basis for selecting a new therapeutic target for osteosarcoma. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12935-018-0612-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-13 /pmc/articles/PMC6090628/ /pubmed/30123092 http://dx.doi.org/10.1186/s12935-018-0612-1 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 Primary Research
Zhuang, Ming
Qiu, Xubin
Cheng, Dong
Zhu, Chenlei
Chen, Liang
MicroRNA-524 promotes cell proliferation by down-regulating PTEN expression in osteosarcoma
title MicroRNA-524 promotes cell proliferation by down-regulating PTEN expression in osteosarcoma
title_full MicroRNA-524 promotes cell proliferation by down-regulating PTEN expression in osteosarcoma
title_fullStr MicroRNA-524 promotes cell proliferation by down-regulating PTEN expression in osteosarcoma
title_full_unstemmed MicroRNA-524 promotes cell proliferation by down-regulating PTEN expression in osteosarcoma
title_short MicroRNA-524 promotes cell proliferation by down-regulating PTEN expression in osteosarcoma
title_sort microrna-524 promotes cell proliferation by down-regulating pten expression in osteosarcoma
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090628/
https://www.ncbi.nlm.nih.gov/pubmed/30123092
http://dx.doi.org/10.1186/s12935-018-0612-1
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