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A serum microRNA signature as a prognostic factor for patients with advanced NSCLC and its association with tissue microRNA expression profiles

The aim of the present study was to detect microRNA (miRNA) signatures in advanced non-small cell lung cancer (NSCLC), and to study the association between miRNA expression levels in serum and tissue. A cohort of patients who had previously been diagnosed with advanced NSCLC was enrolled in the pres...

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Autores principales: GUO, JING, MENG, RUI, YIN, ZHONGYUAN, LI, PENGCHENG, ZHOU, RUI, ZHANG, SHENG, DONG, XIAORONG, LIU, LI, WU, GANG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878579/
https://www.ncbi.nlm.nih.gov/pubmed/27081922
http://dx.doi.org/10.3892/mmr.2016.5114
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author GUO, JING
MENG, RUI
YIN, ZHONGYUAN
LI, PENGCHENG
ZHOU, RUI
ZHANG, SHENG
DONG, XIAORONG
LIU, LI
WU, GANG
author_facet GUO, JING
MENG, RUI
YIN, ZHONGYUAN
LI, PENGCHENG
ZHOU, RUI
ZHANG, SHENG
DONG, XIAORONG
LIU, LI
WU, GANG
author_sort GUO, JING
collection PubMed
description The aim of the present study was to detect microRNA (miRNA) signatures in advanced non-small cell lung cancer (NSCLC), and to study the association between miRNA expression levels in serum and tissue. A cohort of patients who had previously been diagnosed with advanced NSCLC was enrolled in the present study. miRNAs associated with prognosis, which had previously been detected in early stage NSCLC samples, were measured in the serum of the patient groups using a cross-validation method. In addition, serum miRNAs associated with progression-free survival (PFS) were detected in paired fresh tissue samples, in order to analyze the correlation between serum and tissue expression levels. A risk-score analysis was used to develop a four-miRNA signature to predict PFS. miR-1, miR-30d, miR-221 and miR-486 were identified as having a significant correlation with PFS in advanced NSCLC. miR-221 and miR-486 exhibited significant positive correlations between serum and tissue expression. Furthermore, overexpression of miR-221 and reduced expression of miR-486 increased cell proliferation, migration and invasion in vitro. In conclusion, the miRNA signature identified in the present study may be considered an independent prognostic factor of PFS in advanced NSCLC. In addition, the expression levels of miR-221 and miR-486 were significantly correlated between serum and tissue. miR-221 was identified as an oncogenic risk factor, whereas miR-486 exerted protective effects against cancer cell proliferation, migration and invasion.
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spelling pubmed-48785792016-05-25 A serum microRNA signature as a prognostic factor for patients with advanced NSCLC and its association with tissue microRNA expression profiles GUO, JING MENG, RUI YIN, ZHONGYUAN LI, PENGCHENG ZHOU, RUI ZHANG, SHENG DONG, XIAORONG LIU, LI WU, GANG Mol Med Rep Articles The aim of the present study was to detect microRNA (miRNA) signatures in advanced non-small cell lung cancer (NSCLC), and to study the association between miRNA expression levels in serum and tissue. A cohort of patients who had previously been diagnosed with advanced NSCLC was enrolled in the present study. miRNAs associated with prognosis, which had previously been detected in early stage NSCLC samples, were measured in the serum of the patient groups using a cross-validation method. In addition, serum miRNAs associated with progression-free survival (PFS) were detected in paired fresh tissue samples, in order to analyze the correlation between serum and tissue expression levels. A risk-score analysis was used to develop a four-miRNA signature to predict PFS. miR-1, miR-30d, miR-221 and miR-486 were identified as having a significant correlation with PFS in advanced NSCLC. miR-221 and miR-486 exhibited significant positive correlations between serum and tissue expression. Furthermore, overexpression of miR-221 and reduced expression of miR-486 increased cell proliferation, migration and invasion in vitro. In conclusion, the miRNA signature identified in the present study may be considered an independent prognostic factor of PFS in advanced NSCLC. In addition, the expression levels of miR-221 and miR-486 were significantly correlated between serum and tissue. miR-221 was identified as an oncogenic risk factor, whereas miR-486 exerted protective effects against cancer cell proliferation, migration and invasion. D.A. Spandidos 2016-06 2016-04-13 /pmc/articles/PMC4878579/ /pubmed/27081922 http://dx.doi.org/10.3892/mmr.2016.5114 Text en Copyright: © Guo et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
GUO, JING
MENG, RUI
YIN, ZHONGYUAN
LI, PENGCHENG
ZHOU, RUI
ZHANG, SHENG
DONG, XIAORONG
LIU, LI
WU, GANG
A serum microRNA signature as a prognostic factor for patients with advanced NSCLC and its association with tissue microRNA expression profiles
title A serum microRNA signature as a prognostic factor for patients with advanced NSCLC and its association with tissue microRNA expression profiles
title_full A serum microRNA signature as a prognostic factor for patients with advanced NSCLC and its association with tissue microRNA expression profiles
title_fullStr A serum microRNA signature as a prognostic factor for patients with advanced NSCLC and its association with tissue microRNA expression profiles
title_full_unstemmed A serum microRNA signature as a prognostic factor for patients with advanced NSCLC and its association with tissue microRNA expression profiles
title_short A serum microRNA signature as a prognostic factor for patients with advanced NSCLC and its association with tissue microRNA expression profiles
title_sort serum microrna signature as a prognostic factor for patients with advanced nsclc and its association with tissue microrna expression profiles
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878579/
https://www.ncbi.nlm.nih.gov/pubmed/27081922
http://dx.doi.org/10.3892/mmr.2016.5114
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