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Identification of a Plasma Four-microRNA Panel as Potential Noninvasive Biomarker for Osteosarcoma

BACKGROUND: Circulating microRNAs (miRNAs) are emerging as promising biomarkers for human cancer. Osteosarcoma is the most common human primary malignant bone tumor in children and young adults. The objective of this study was to investigate whether circulating miRNAs in plasma could be a useful bio...

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Autores principales: Lian, Feng, Cui, Yong, Zhou, Chenliang, Gao, Kewei, Wu, Liwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361617/
https://www.ncbi.nlm.nih.gov/pubmed/25775010
http://dx.doi.org/10.1371/journal.pone.0121499
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author Lian, Feng
Cui, Yong
Zhou, Chenliang
Gao, Kewei
Wu, Liwen
author_facet Lian, Feng
Cui, Yong
Zhou, Chenliang
Gao, Kewei
Wu, Liwen
author_sort Lian, Feng
collection PubMed
description BACKGROUND: Circulating microRNAs (miRNAs) are emerging as promising biomarkers for human cancer. Osteosarcoma is the most common human primary malignant bone tumor in children and young adults. The objective of this study was to investigate whether circulating miRNAs in plasma could be a useful biomarker for detecting osteosarcoma and monitoring tumor removal dynamics. METHODS: Plasma samples were obtained from 90 patients before surgery, 50 patients after one month of surgery, and 90 healthy individuals. The study was divided into three steps: First, initial screening of the profiles of circulating miRNAs in pooled plasma samples from healthy controls and pre-operative osteosarcoma patients using a TaqMan low density array (TLDA). Second, evaluation of miRNA concentration in individual plasma samples from 90 pre-operative osteosarcoma patients and 90 healthy controls by a quantitative real time PCR (qRT-PCR) assay. Third, evaluation of miRNA concentration in paired plasma samples from 50 pre- and post-operative osteosarcoma patients by qRT-PCR assay. RESULTS: Four plasma miRNAs including miR-195-5p, miR-199a-3p, miR-320a, and miR-374a-5p were significantly increased in the osteosarcoma patients. Receiver operating characteristics curve analysis of the combined populations demonstrated that the four-miRNA signature could discriminate cases from controls with an area under the curve of 0.9608 (95% CI 0.9307-0.9912). These 4 miRNAs were markedly decreased in the plasma after operation. In addition, circulating miR-195-5p and miR-199a-3p were correlated with metastasis status, while miR-199a-3p and miR-320a were correlated with histological subtype. CONCLUSIONS: Our data suggest that altered levels of circulating miRNAs might have great potential to serve as novel, non-invasive biomarkers for osteosarcoma.
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spelling pubmed-43616172015-03-23 Identification of a Plasma Four-microRNA Panel as Potential Noninvasive Biomarker for Osteosarcoma Lian, Feng Cui, Yong Zhou, Chenliang Gao, Kewei Wu, Liwen PLoS One Research Article BACKGROUND: Circulating microRNAs (miRNAs) are emerging as promising biomarkers for human cancer. Osteosarcoma is the most common human primary malignant bone tumor in children and young adults. The objective of this study was to investigate whether circulating miRNAs in plasma could be a useful biomarker for detecting osteosarcoma and monitoring tumor removal dynamics. METHODS: Plasma samples were obtained from 90 patients before surgery, 50 patients after one month of surgery, and 90 healthy individuals. The study was divided into three steps: First, initial screening of the profiles of circulating miRNAs in pooled plasma samples from healthy controls and pre-operative osteosarcoma patients using a TaqMan low density array (TLDA). Second, evaluation of miRNA concentration in individual plasma samples from 90 pre-operative osteosarcoma patients and 90 healthy controls by a quantitative real time PCR (qRT-PCR) assay. Third, evaluation of miRNA concentration in paired plasma samples from 50 pre- and post-operative osteosarcoma patients by qRT-PCR assay. RESULTS: Four plasma miRNAs including miR-195-5p, miR-199a-3p, miR-320a, and miR-374a-5p were significantly increased in the osteosarcoma patients. Receiver operating characteristics curve analysis of the combined populations demonstrated that the four-miRNA signature could discriminate cases from controls with an area under the curve of 0.9608 (95% CI 0.9307-0.9912). These 4 miRNAs were markedly decreased in the plasma after operation. In addition, circulating miR-195-5p and miR-199a-3p were correlated with metastasis status, while miR-199a-3p and miR-320a were correlated with histological subtype. CONCLUSIONS: Our data suggest that altered levels of circulating miRNAs might have great potential to serve as novel, non-invasive biomarkers for osteosarcoma. Public Library of Science 2015-03-16 /pmc/articles/PMC4361617/ /pubmed/25775010 http://dx.doi.org/10.1371/journal.pone.0121499 Text en © 2015 Lian et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lian, Feng
Cui, Yong
Zhou, Chenliang
Gao, Kewei
Wu, Liwen
Identification of a Plasma Four-microRNA Panel as Potential Noninvasive Biomarker for Osteosarcoma
title Identification of a Plasma Four-microRNA Panel as Potential Noninvasive Biomarker for Osteosarcoma
title_full Identification of a Plasma Four-microRNA Panel as Potential Noninvasive Biomarker for Osteosarcoma
title_fullStr Identification of a Plasma Four-microRNA Panel as Potential Noninvasive Biomarker for Osteosarcoma
title_full_unstemmed Identification of a Plasma Four-microRNA Panel as Potential Noninvasive Biomarker for Osteosarcoma
title_short Identification of a Plasma Four-microRNA Panel as Potential Noninvasive Biomarker for Osteosarcoma
title_sort identification of a plasma four-microrna panel as potential noninvasive biomarker for osteosarcoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361617/
https://www.ncbi.nlm.nih.gov/pubmed/25775010
http://dx.doi.org/10.1371/journal.pone.0121499
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