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miR-630 functions as a tumor oncogene in renal cell carcinoma
INTRODUCTION: MicroRNAs (miRNAs) are non-coding RNAs that regulate multiple cell processes during cancer progression. Renal cell carcinoma (RCC) is a malignancy with a poor prognosis. In this study, we aimed to investigate the roles of miR-630 in RCC progression. MATERIAL AND METHODS: Expression of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889681/ https://www.ncbi.nlm.nih.gov/pubmed/27279836 http://dx.doi.org/10.5114/aoms.2016.59918 |
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author | Zhao, Jian-Jun Chen, Peng-Jie Duan, Rui-Qin Li, Ke-Ji Wang, Yu-Zhong Li, Yong |
author_facet | Zhao, Jian-Jun Chen, Peng-Jie Duan, Rui-Qin Li, Ke-Ji Wang, Yu-Zhong Li, Yong |
author_sort | Zhao, Jian-Jun |
collection | PubMed |
description | INTRODUCTION: MicroRNAs (miRNAs) are non-coding RNAs that regulate multiple cell processes during cancer progression. Renal cell carcinoma (RCC) is a malignancy with a poor prognosis. In this study, we aimed to investigate the roles of miR-630 in RCC progression. MATERIAL AND METHODS: Expression of miR-630 was evaluated by quantitative real-time polymerase chain reaction (qRT-PCR) in four renal cancer cell lines (786-O, ACHN, Caki-1, and Caki-2) and one normal human proximal tubule epithelial cell line (HK-2). Next, miR-630 inhibitor was used to inhibit miR-630 expression in 786-O cells. Finally, its effects on cell proliferation, apoptosis, migration, and invasion were evaluated. RESULTS: The expression level of miR-630 was higher in renal cancer cell lines 786-O, ACHN, Caki-1, and Caki-2 than that in the normal renal cell line HK-2 (p < 0.05). Furthermore, a proliferation assay, apoptosis assay, migration assay and invasion assay were performed, and the results showed that down-regulation of miR-630 expression by miR-630 inhibitor significantly inhibited cell proliferation, migration, and invasion, which meanwhile induced cell apoptosis of the renal cancer cell line 786-O. CONCLUSIONS: This is the first time that miR-630 expression has been shown to be associated with renal cancer progression, and down-regulation of miR-630 can inhibit tumor progression, which provides a potential therapeutic target for renal cancer treatment. |
format | Online Article Text |
id | pubmed-4889681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-48896812016-06-08 miR-630 functions as a tumor oncogene in renal cell carcinoma Zhao, Jian-Jun Chen, Peng-Jie Duan, Rui-Qin Li, Ke-Ji Wang, Yu-Zhong Li, Yong Arch Med Sci Basic Research INTRODUCTION: MicroRNAs (miRNAs) are non-coding RNAs that regulate multiple cell processes during cancer progression. Renal cell carcinoma (RCC) is a malignancy with a poor prognosis. In this study, we aimed to investigate the roles of miR-630 in RCC progression. MATERIAL AND METHODS: Expression of miR-630 was evaluated by quantitative real-time polymerase chain reaction (qRT-PCR) in four renal cancer cell lines (786-O, ACHN, Caki-1, and Caki-2) and one normal human proximal tubule epithelial cell line (HK-2). Next, miR-630 inhibitor was used to inhibit miR-630 expression in 786-O cells. Finally, its effects on cell proliferation, apoptosis, migration, and invasion were evaluated. RESULTS: The expression level of miR-630 was higher in renal cancer cell lines 786-O, ACHN, Caki-1, and Caki-2 than that in the normal renal cell line HK-2 (p < 0.05). Furthermore, a proliferation assay, apoptosis assay, migration assay and invasion assay were performed, and the results showed that down-regulation of miR-630 expression by miR-630 inhibitor significantly inhibited cell proliferation, migration, and invasion, which meanwhile induced cell apoptosis of the renal cancer cell line 786-O. CONCLUSIONS: This is the first time that miR-630 expression has been shown to be associated with renal cancer progression, and down-regulation of miR-630 can inhibit tumor progression, which provides a potential therapeutic target for renal cancer treatment. Termedia Publishing House 2016-05-18 2016-06-01 /pmc/articles/PMC4889681/ /pubmed/27279836 http://dx.doi.org/10.5114/aoms.2016.59918 Text en Copyright © 2016 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Basic Research Zhao, Jian-Jun Chen, Peng-Jie Duan, Rui-Qin Li, Ke-Ji Wang, Yu-Zhong Li, Yong miR-630 functions as a tumor oncogene in renal cell carcinoma |
title | miR-630 functions as a tumor oncogene in renal cell carcinoma |
title_full | miR-630 functions as a tumor oncogene in renal cell carcinoma |
title_fullStr | miR-630 functions as a tumor oncogene in renal cell carcinoma |
title_full_unstemmed | miR-630 functions as a tumor oncogene in renal cell carcinoma |
title_short | miR-630 functions as a tumor oncogene in renal cell carcinoma |
title_sort | mir-630 functions as a tumor oncogene in renal cell carcinoma |
topic | Basic Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889681/ https://www.ncbi.nlm.nih.gov/pubmed/27279836 http://dx.doi.org/10.5114/aoms.2016.59918 |
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