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Identification of A Panel of Serum microRNAs as Biomarkers for Early Detection of Lung Adenocarcinoma

Introduction: Since currently no sensitive and specific biomarkers for early detection of lung adenocarcinoma (AD) exist and the majority of AD patients are diagnosed at late stages of disease, the development of effective screening tests for early-stage lung AD is urgently needed. Serum microRNAs (...

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Autores principales: Lv, Shaogang, Xue, Jian, Wu, Chuanyong, Wang, Lin, Wu, Jing, Xu, Shujun, Liang, Xiaohui, Lou, Jiatao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5264039/
https://www.ncbi.nlm.nih.gov/pubmed/28123597
http://dx.doi.org/10.7150/jca.16644
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author Lv, Shaogang
Xue, Jian
Wu, Chuanyong
Wang, Lin
Wu, Jing
Xu, Shujun
Liang, Xiaohui
Lou, Jiatao
author_facet Lv, Shaogang
Xue, Jian
Wu, Chuanyong
Wang, Lin
Wu, Jing
Xu, Shujun
Liang, Xiaohui
Lou, Jiatao
author_sort Lv, Shaogang
collection PubMed
description Introduction: Since currently no sensitive and specific biomarkers for early detection of lung adenocarcinoma (AD) exist and the majority of AD patients are diagnosed at late stages of disease, the development of effective screening tests for early-stage lung AD is urgently needed. Serum microRNAs (miRNAs) have been documented as novel noninvasive biomarkers in tumor diagnosis; thus, we studied the profile of serum miRNA in AD patients in order to identify the differentially expressed miRNAs as potential biomarkers for early detection of AD. Patients and Methods: Serum samples were collected from 180 AD patients and 180 age- and sex-matched healthy controls. Serum miRNA profiling was performed by low-density array (LDA) using RNA extracted from blood samples of 20 patients and 20 controls. To validate the selected miRNAs, a stem-loop based RT-qPCR assay was used and serum samples from 160 patients and 160 controls were examined. Results: Profiling data showed 11 differentially expressed miRNAs in the serum samples from AD patients compared with the controls. Among them, 6 selected miRNAs in AD patients, including miR-103, miR-146a, miR-151, miR-21, miR-221, miR-222, and miR-223, were validated by RT-qPCR. In particular, the top three, miR-146a, miR-222, and miR-223, were confirmed to be significantly expressed in stage I/II AD patients compared with healthy controls. Conclusion: A panel of miRNAs with miR-146a, miR-222 and miR-223 could be used as potential noninvasive biomarkers for early detection of AD.
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spelling pubmed-52640392017-01-25 Identification of A Panel of Serum microRNAs as Biomarkers for Early Detection of Lung Adenocarcinoma Lv, Shaogang Xue, Jian Wu, Chuanyong Wang, Lin Wu, Jing Xu, Shujun Liang, Xiaohui Lou, Jiatao J Cancer Research Paper Introduction: Since currently no sensitive and specific biomarkers for early detection of lung adenocarcinoma (AD) exist and the majority of AD patients are diagnosed at late stages of disease, the development of effective screening tests for early-stage lung AD is urgently needed. Serum microRNAs (miRNAs) have been documented as novel noninvasive biomarkers in tumor diagnosis; thus, we studied the profile of serum miRNA in AD patients in order to identify the differentially expressed miRNAs as potential biomarkers for early detection of AD. Patients and Methods: Serum samples were collected from 180 AD patients and 180 age- and sex-matched healthy controls. Serum miRNA profiling was performed by low-density array (LDA) using RNA extracted from blood samples of 20 patients and 20 controls. To validate the selected miRNAs, a stem-loop based RT-qPCR assay was used and serum samples from 160 patients and 160 controls were examined. Results: Profiling data showed 11 differentially expressed miRNAs in the serum samples from AD patients compared with the controls. Among them, 6 selected miRNAs in AD patients, including miR-103, miR-146a, miR-151, miR-21, miR-221, miR-222, and miR-223, were validated by RT-qPCR. In particular, the top three, miR-146a, miR-222, and miR-223, were confirmed to be significantly expressed in stage I/II AD patients compared with healthy controls. Conclusion: A panel of miRNAs with miR-146a, miR-222 and miR-223 could be used as potential noninvasive biomarkers for early detection of AD. Ivyspring International Publisher 2017-01-01 /pmc/articles/PMC5264039/ /pubmed/28123597 http://dx.doi.org/10.7150/jca.16644 Text en © Ivyspring International Publisher. This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Lv, Shaogang
Xue, Jian
Wu, Chuanyong
Wang, Lin
Wu, Jing
Xu, Shujun
Liang, Xiaohui
Lou, Jiatao
Identification of A Panel of Serum microRNAs as Biomarkers for Early Detection of Lung Adenocarcinoma
title Identification of A Panel of Serum microRNAs as Biomarkers for Early Detection of Lung Adenocarcinoma
title_full Identification of A Panel of Serum microRNAs as Biomarkers for Early Detection of Lung Adenocarcinoma
title_fullStr Identification of A Panel of Serum microRNAs as Biomarkers for Early Detection of Lung Adenocarcinoma
title_full_unstemmed Identification of A Panel of Serum microRNAs as Biomarkers for Early Detection of Lung Adenocarcinoma
title_short Identification of A Panel of Serum microRNAs as Biomarkers for Early Detection of Lung Adenocarcinoma
title_sort identification of a panel of serum micrornas as biomarkers for early detection of lung adenocarcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5264039/
https://www.ncbi.nlm.nih.gov/pubmed/28123597
http://dx.doi.org/10.7150/jca.16644
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