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Tissue microRNA-126 expression level predicts outcome in human osteosarcoma

BACKGROUND: MicroRNA-126 has been found to be consistently under-expressed in osteosarcoma tissues and cell lines compared with normal bone tissues and normal osteoblast cells, respectively. The purpose of the present study was to detect the expression levels of miR-126 in osteosarcoma patients and...

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Autores principales: Liu, Wei, Zhao, Zhong-yuan, Shi, Lei, Yuan, Wen-dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4509614/
https://www.ncbi.nlm.nih.gov/pubmed/26194657
http://dx.doi.org/10.1186/s13000-015-0329-6
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author Liu, Wei
Zhao, Zhong-yuan
Shi, Lei
Yuan, Wen-dan
author_facet Liu, Wei
Zhao, Zhong-yuan
Shi, Lei
Yuan, Wen-dan
author_sort Liu, Wei
collection PubMed
description BACKGROUND: MicroRNA-126 has been found to be consistently under-expressed in osteosarcoma tissues and cell lines compared with normal bone tissues and normal osteoblast cells, respectively. The purpose of the present study was to detect the expression levels of miR-126 in osteosarcoma patients and to further investigate the clinicopathological, and prognostic value of miR-126. METHODS: We recruited 122 patients with osteosarcomas from the Department of Orthopedic Surgery, Yantaishan Hospital between May 2008 and April 2013. The expression level of miR-126 was determined by qRT-PCR. Associations between miR-126 expression and various clinicopathological characteristics were analyzed using the χ(2) test. Survival rate was determined with Kaplan-Meier and statistically analyzed with the log-rank method between groups. Survival data were evaluated through multivariate Cox regression analysis. RESULTS: miR-126 expression was significantly decreased in osteosarcoma tissues compared to adjacent normal bone tissues (2.421 ± 1.250 vs. 6.212 ± 1.843, P = 0.001). We found that low miR-126 expression had significant association with advanced TNM stage (P <0.001), distant metastasis (P <0.001), and higher tumor grade (P = 0.001). Kaplan-Meier survival analysis showed that the miR-126 low-expression group had significantly shorter overall survival time than those with high-expression (log-rank test, P = 0.008). Furthermore, multivariate Cox proportional hazards model analysis showed that miR-126 expression was independently associated with overall survival of patients with osteosarcoma (HR = 3.102, 95 % CI: 1.113–9.023, P = 0.018). CONCLUSIONS: This is the first study revealing that miR-126 down-expression may be related to the prediction of poor prognosis for osteosarcoma patients, suggesting that miR-126 may serve as a prognostic marker for the optimization of clinical treatments.
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spelling pubmed-45096142015-07-22 Tissue microRNA-126 expression level predicts outcome in human osteosarcoma Liu, Wei Zhao, Zhong-yuan Shi, Lei Yuan, Wen-dan Diagn Pathol Research BACKGROUND: MicroRNA-126 has been found to be consistently under-expressed in osteosarcoma tissues and cell lines compared with normal bone tissues and normal osteoblast cells, respectively. The purpose of the present study was to detect the expression levels of miR-126 in osteosarcoma patients and to further investigate the clinicopathological, and prognostic value of miR-126. METHODS: We recruited 122 patients with osteosarcomas from the Department of Orthopedic Surgery, Yantaishan Hospital between May 2008 and April 2013. The expression level of miR-126 was determined by qRT-PCR. Associations between miR-126 expression and various clinicopathological characteristics were analyzed using the χ(2) test. Survival rate was determined with Kaplan-Meier and statistically analyzed with the log-rank method between groups. Survival data were evaluated through multivariate Cox regression analysis. RESULTS: miR-126 expression was significantly decreased in osteosarcoma tissues compared to adjacent normal bone tissues (2.421 ± 1.250 vs. 6.212 ± 1.843, P = 0.001). We found that low miR-126 expression had significant association with advanced TNM stage (P <0.001), distant metastasis (P <0.001), and higher tumor grade (P = 0.001). Kaplan-Meier survival analysis showed that the miR-126 low-expression group had significantly shorter overall survival time than those with high-expression (log-rank test, P = 0.008). Furthermore, multivariate Cox proportional hazards model analysis showed that miR-126 expression was independently associated with overall survival of patients with osteosarcoma (HR = 3.102, 95 % CI: 1.113–9.023, P = 0.018). CONCLUSIONS: This is the first study revealing that miR-126 down-expression may be related to the prediction of poor prognosis for osteosarcoma patients, suggesting that miR-126 may serve as a prognostic marker for the optimization of clinical treatments. BioMed Central 2015-07-21 /pmc/articles/PMC4509614/ /pubmed/26194657 http://dx.doi.org/10.1186/s13000-015-0329-6 Text en © Liu et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Research
Liu, Wei
Zhao, Zhong-yuan
Shi, Lei
Yuan, Wen-dan
Tissue microRNA-126 expression level predicts outcome in human osteosarcoma
title Tissue microRNA-126 expression level predicts outcome in human osteosarcoma
title_full Tissue microRNA-126 expression level predicts outcome in human osteosarcoma
title_fullStr Tissue microRNA-126 expression level predicts outcome in human osteosarcoma
title_full_unstemmed Tissue microRNA-126 expression level predicts outcome in human osteosarcoma
title_short Tissue microRNA-126 expression level predicts outcome in human osteosarcoma
title_sort tissue microrna-126 expression level predicts outcome in human osteosarcoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4509614/
https://www.ncbi.nlm.nih.gov/pubmed/26194657
http://dx.doi.org/10.1186/s13000-015-0329-6
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