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Down-regulation of microRNA-182 and microRNA-183 predicts progression of osteosarcoma
INTRODUCTION: The aim of this study was to investigate the expression levels of microRNA-182 and microRNA-183 and their association with clinicopathological features in patients with osteosarcoma. MATERIAL AND METHODS: Total RNA was purified from samples and noncancerous bone tissues and then quanti...
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/PMC5701680/ https://www.ncbi.nlm.nih.gov/pubmed/29181065 http://dx.doi.org/10.5114/aoms.2016.60091 |
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author | Golbakhsh, Mohammad Reza Boddouhi, Bahram Hatami, Negin Goudarzi, Peyman Karimi Shakeri, Mohammadreza Yahaghi, Emad Taheriazam, Afshin |
author_facet | Golbakhsh, Mohammad Reza Boddouhi, Bahram Hatami, Negin Goudarzi, Peyman Karimi Shakeri, Mohammadreza Yahaghi, Emad Taheriazam, Afshin |
author_sort | Golbakhsh, Mohammad Reza |
collection | PubMed |
description | INTRODUCTION: The aim of this study was to investigate the expression levels of microRNA-182 and microRNA-183 and their association with clinicopathological features in patients with osteosarcoma. MATERIAL AND METHODS: Total RNA was purified from samples and noncancerous bone tissues and then quantitative real-time polymerase chain reaction was applied to evaluate the expression levels of microRNAs, and their relationship with clinicopathological features and survival in osteosarcoma patients. RESULTS: Our findings showed that expression of MiR-182 was clearly lower in osteosarcoma bone tissue (mean ± SD: 2.84 ±.07) compared with noncancerous bone tissues (6.23 ±1.72, p = 0.004). On the other hand, lower expression of MiR-183 was seen in osteosarcoma bone tissue (1.43 ±0.59) when compared with normal tissues (4.36 ±2.47, p = 0.036). Decreased expression of MiR-182 was clearly correlated with advanced clinical stage (p = 0.001), metastasis or recurrence (p = 0.024), and large tumor size (p = 0.032). Decreased expression of MiR-183 was associated with advanced TNM stage (p = 0.004), and metastasis or recurrence (p = 0.002). A multivariate Cox proportional hazards model revealed that low expression of MiR-182 and MiR-183 (p = 0.02; p = 0.016), TNM stage (p = 0.04), and metastasis or recurrence (p = 0.03) were significantly associated with poor survival as independent prognostic factors. CONCLUSIONS: These findings suggest that MiR-182 and MiR-183 may be associated with progression and metastasis of osteosarcoma. |
format | Online Article Text |
id | pubmed-5701680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-57016802017-11-27 Down-regulation of microRNA-182 and microRNA-183 predicts progression of osteosarcoma Golbakhsh, Mohammad Reza Boddouhi, Bahram Hatami, Negin Goudarzi, Peyman Karimi Shakeri, Mohammadreza Yahaghi, Emad Taheriazam, Afshin Arch Med Sci Basic Research INTRODUCTION: The aim of this study was to investigate the expression levels of microRNA-182 and microRNA-183 and their association with clinicopathological features in patients with osteosarcoma. MATERIAL AND METHODS: Total RNA was purified from samples and noncancerous bone tissues and then quantitative real-time polymerase chain reaction was applied to evaluate the expression levels of microRNAs, and their relationship with clinicopathological features and survival in osteosarcoma patients. RESULTS: Our findings showed that expression of MiR-182 was clearly lower in osteosarcoma bone tissue (mean ± SD: 2.84 ±.07) compared with noncancerous bone tissues (6.23 ±1.72, p = 0.004). On the other hand, lower expression of MiR-183 was seen in osteosarcoma bone tissue (1.43 ±0.59) when compared with normal tissues (4.36 ±2.47, p = 0.036). Decreased expression of MiR-182 was clearly correlated with advanced clinical stage (p = 0.001), metastasis or recurrence (p = 0.024), and large tumor size (p = 0.032). Decreased expression of MiR-183 was associated with advanced TNM stage (p = 0.004), and metastasis or recurrence (p = 0.002). A multivariate Cox proportional hazards model revealed that low expression of MiR-182 and MiR-183 (p = 0.02; p = 0.016), TNM stage (p = 0.04), and metastasis or recurrence (p = 0.03) were significantly associated with poor survival as independent prognostic factors. CONCLUSIONS: These findings suggest that MiR-182 and MiR-183 may be associated with progression and metastasis of osteosarcoma. Termedia Publishing House 2016-05-20 2017-10 /pmc/articles/PMC5701680/ /pubmed/29181065 http://dx.doi.org/10.5114/aoms.2016.60091 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 Golbakhsh, Mohammad Reza Boddouhi, Bahram Hatami, Negin Goudarzi, Peyman Karimi Shakeri, Mohammadreza Yahaghi, Emad Taheriazam, Afshin Down-regulation of microRNA-182 and microRNA-183 predicts progression of osteosarcoma |
title | Down-regulation of microRNA-182 and microRNA-183 predicts progression of osteosarcoma |
title_full | Down-regulation of microRNA-182 and microRNA-183 predicts progression of osteosarcoma |
title_fullStr | Down-regulation of microRNA-182 and microRNA-183 predicts progression of osteosarcoma |
title_full_unstemmed | Down-regulation of microRNA-182 and microRNA-183 predicts progression of osteosarcoma |
title_short | Down-regulation of microRNA-182 and microRNA-183 predicts progression of osteosarcoma |
title_sort | down-regulation of microrna-182 and microrna-183 predicts progression of osteosarcoma |
topic | Basic Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701680/ https://www.ncbi.nlm.nih.gov/pubmed/29181065 http://dx.doi.org/10.5114/aoms.2016.60091 |
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