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Association of circulating miR-125b and survival in patients with osteosarcoma–A single center experience

BACKGROUND: It is known that miRNAs play various roles in malignant tumors. This study is designed to investigate whether miR-125b levels can be used to predict the clinical response of patients with osteosarcoma (OS) to cisplatin-based chemotherapy. METHODS: From January 2010 to July 2015, 82 patie...

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Autores principales: Luo, Zhiqiang, Liu, Minglu, Zhang, Haihong, Xia, Yayi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154701/
https://www.ncbi.nlm.nih.gov/pubmed/28008378
http://dx.doi.org/10.1016/j.jbo.2016.06.002
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author Luo, Zhiqiang
Liu, Minglu
Zhang, Haihong
Xia, Yayi
author_facet Luo, Zhiqiang
Liu, Minglu
Zhang, Haihong
Xia, Yayi
author_sort Luo, Zhiqiang
collection PubMed
description BACKGROUND: It is known that miRNAs play various roles in malignant tumors. This study is designed to investigate whether miR-125b levels can be used to predict the clinical response of patients with osteosarcoma (OS) to cisplatin-based chemotherapy. METHODS: From January 2010 to July 2015, 82 patients with resectable OS and 56 patients with unresectable OS were enrolled. Blood samples were collected and quantitative real-time PCR was applied to determine miR-125b expression. Clinical data was collected through medical records, and patients were treated according to National Comprehensive Cancer Network guidelines on OS. RESULTS: Our study found that patients with low miR-125b expression had shorter disease-free survival (p<0.001) in the OS group, which was verified by Kaplan-Meier analysis and univariate and multivariate Cox analyses (p<0.001). For patients with unresectable OS, low miR-125b expression was found to be associated with advanced tumor stages (p=0.006). No complete remission was observed, and there were 13 patients with partial remission, 21 with stable disease, and 22 with disease progression. Negative correlation was found between miR-125b expression and response to chemotherapy (p<0.001, r=−0.606). Furthermore, ROC analysis indicated that miR-125b at the cut point of 0.61 yielded an area under the ROC curve of 0.793 (p<0.001, 95% CI: 0.664–0.890) in distinguishing chemotherapy-resistant OS from chemotherapy-sensitive OS, with sensitivity and specificity at 76.9% and 79.1%, respectively. Kaplan-Meier analysis and univariate and multivariate Cox analyses showed that patients with low miR-125b expression suffered shorter overall survival (p=0.014, p=0.024, and p=0.049, respectively). CONCLUSION: Down-regulation of circulating miR-125b might have the potential to predict cisplatin-based chemotherapy resistance and poor prognosis in OS.
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spelling pubmed-51547012016-12-22 Association of circulating miR-125b and survival in patients with osteosarcoma–A single center experience Luo, Zhiqiang Liu, Minglu Zhang, Haihong Xia, Yayi J Bone Oncol Research Paper BACKGROUND: It is known that miRNAs play various roles in malignant tumors. This study is designed to investigate whether miR-125b levels can be used to predict the clinical response of patients with osteosarcoma (OS) to cisplatin-based chemotherapy. METHODS: From January 2010 to July 2015, 82 patients with resectable OS and 56 patients with unresectable OS were enrolled. Blood samples were collected and quantitative real-time PCR was applied to determine miR-125b expression. Clinical data was collected through medical records, and patients were treated according to National Comprehensive Cancer Network guidelines on OS. RESULTS: Our study found that patients with low miR-125b expression had shorter disease-free survival (p<0.001) in the OS group, which was verified by Kaplan-Meier analysis and univariate and multivariate Cox analyses (p<0.001). For patients with unresectable OS, low miR-125b expression was found to be associated with advanced tumor stages (p=0.006). No complete remission was observed, and there were 13 patients with partial remission, 21 with stable disease, and 22 with disease progression. Negative correlation was found between miR-125b expression and response to chemotherapy (p<0.001, r=−0.606). Furthermore, ROC analysis indicated that miR-125b at the cut point of 0.61 yielded an area under the ROC curve of 0.793 (p<0.001, 95% CI: 0.664–0.890) in distinguishing chemotherapy-resistant OS from chemotherapy-sensitive OS, with sensitivity and specificity at 76.9% and 79.1%, respectively. Kaplan-Meier analysis and univariate and multivariate Cox analyses showed that patients with low miR-125b expression suffered shorter overall survival (p=0.014, p=0.024, and p=0.049, respectively). CONCLUSION: Down-regulation of circulating miR-125b might have the potential to predict cisplatin-based chemotherapy resistance and poor prognosis in OS. Elsevier 2016-06-16 /pmc/articles/PMC5154701/ /pubmed/28008378 http://dx.doi.org/10.1016/j.jbo.2016.06.002 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Luo, Zhiqiang
Liu, Minglu
Zhang, Haihong
Xia, Yayi
Association of circulating miR-125b and survival in patients with osteosarcoma–A single center experience
title Association of circulating miR-125b and survival in patients with osteosarcoma–A single center experience
title_full Association of circulating miR-125b and survival in patients with osteosarcoma–A single center experience
title_fullStr Association of circulating miR-125b and survival in patients with osteosarcoma–A single center experience
title_full_unstemmed Association of circulating miR-125b and survival in patients with osteosarcoma–A single center experience
title_short Association of circulating miR-125b and survival in patients with osteosarcoma–A single center experience
title_sort association of circulating mir-125b and survival in patients with osteosarcoma–a single center experience
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154701/
https://www.ncbi.nlm.nih.gov/pubmed/28008378
http://dx.doi.org/10.1016/j.jbo.2016.06.002
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