Cargando…

A three-microRNA signature for lung squamous cell carcinoma diagnosis in Chinese male patients

Various studies have demonstrated the diagnostic value of microRNA (miRNA) for lung cancer, but miRNA signatures varied between different subtypes. Whether serum miRNAs could be used as biomarkers in lung squamous cell carcinoma (SCC) remains unknown. Using quantitative real-time polymerase chain re...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Lan, Shan, Xia, Wang, Jun, Zhu, Jun, Huang, Zebo, Zhang, Huo, Zhou, Xin, Cheng, Wenfang, Shu, Yongqian, Zhu, Wei, Liu, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689734/
https://www.ncbi.nlm.nih.gov/pubmed/29156844
http://dx.doi.org/10.18632/oncotarget.19666
_version_ 1783279446945431552
author Zhang, Lan
Shan, Xia
Wang, Jun
Zhu, Jun
Huang, Zebo
Zhang, Huo
Zhou, Xin
Cheng, Wenfang
Shu, Yongqian
Zhu, Wei
Liu, Ping
author_facet Zhang, Lan
Shan, Xia
Wang, Jun
Zhu, Jun
Huang, Zebo
Zhang, Huo
Zhou, Xin
Cheng, Wenfang
Shu, Yongqian
Zhu, Wei
Liu, Ping
author_sort Zhang, Lan
collection PubMed
description Various studies have demonstrated the diagnostic value of microRNA (miRNA) for lung cancer, but miRNA signatures varied between different subtypes. Whether serum miRNAs could be used as biomarkers in lung squamous cell carcinoma (SCC) remains unknown. Using quantitative real-time polymerase chain reaction (qRT-PCR) based Exiqon panel, 38 differentially expressed miRNAs were identified from 3 male lung SCC pool samples and 1 normal control (NC) pool in the initial screening phase. After the training (24 SCC VS. 15 NCs), testing (44 SCC VS. 57 NCs) and external validation (34 SCC VS. 36 NCs VS. 10 pulmonary hamartoma) processes via qRT-PCR, we identified a three-miRNA panel ((miR-106a-5p, miR-20a-5p and miR-93-5p) to be a potential diagnostic marker for male lung SCC patients. The areas under the receiver operating characteristic (ROC) curve of the three-miRNA panel for the training, testing and validation phases were 0.969, 0.881 and 0.954 respectively. In addition, this signature could also differentiate lung SCC from pulmonary hamartoma (AUC=0.900). The 3 miRNAs were consistently up-regulated in lung SCC tissues (23 SCC VS. 23 NCs) and serum exosomes (17 SCC VS. 24 NCs). Moreover, expression of the 3 miRNAs was decreased in arterial serum (n = 3). In conclusion, we established a three-miRNA signature in the peripheral serum with considerable clinical value in the diagnosis of male lung SCC patients.
format Online
Article
Text
id pubmed-5689734
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-56897342017-11-17 A three-microRNA signature for lung squamous cell carcinoma diagnosis in Chinese male patients Zhang, Lan Shan, Xia Wang, Jun Zhu, Jun Huang, Zebo Zhang, Huo Zhou, Xin Cheng, Wenfang Shu, Yongqian Zhu, Wei Liu, Ping Oncotarget Clinical Research Paper Various studies have demonstrated the diagnostic value of microRNA (miRNA) for lung cancer, but miRNA signatures varied between different subtypes. Whether serum miRNAs could be used as biomarkers in lung squamous cell carcinoma (SCC) remains unknown. Using quantitative real-time polymerase chain reaction (qRT-PCR) based Exiqon panel, 38 differentially expressed miRNAs were identified from 3 male lung SCC pool samples and 1 normal control (NC) pool in the initial screening phase. After the training (24 SCC VS. 15 NCs), testing (44 SCC VS. 57 NCs) and external validation (34 SCC VS. 36 NCs VS. 10 pulmonary hamartoma) processes via qRT-PCR, we identified a three-miRNA panel ((miR-106a-5p, miR-20a-5p and miR-93-5p) to be a potential diagnostic marker for male lung SCC patients. The areas under the receiver operating characteristic (ROC) curve of the three-miRNA panel for the training, testing and validation phases were 0.969, 0.881 and 0.954 respectively. In addition, this signature could also differentiate lung SCC from pulmonary hamartoma (AUC=0.900). The 3 miRNAs were consistently up-regulated in lung SCC tissues (23 SCC VS. 23 NCs) and serum exosomes (17 SCC VS. 24 NCs). Moreover, expression of the 3 miRNAs was decreased in arterial serum (n = 3). In conclusion, we established a three-miRNA signature in the peripheral serum with considerable clinical value in the diagnosis of male lung SCC patients. Impact Journals LLC 2017-07-28 /pmc/articles/PMC5689734/ /pubmed/29156844 http://dx.doi.org/10.18632/oncotarget.19666 Text en Copyright: © 2017 Zhang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Zhang, Lan
Shan, Xia
Wang, Jun
Zhu, Jun
Huang, Zebo
Zhang, Huo
Zhou, Xin
Cheng, Wenfang
Shu, Yongqian
Zhu, Wei
Liu, Ping
A three-microRNA signature for lung squamous cell carcinoma diagnosis in Chinese male patients
title A three-microRNA signature for lung squamous cell carcinoma diagnosis in Chinese male patients
title_full A three-microRNA signature for lung squamous cell carcinoma diagnosis in Chinese male patients
title_fullStr A three-microRNA signature for lung squamous cell carcinoma diagnosis in Chinese male patients
title_full_unstemmed A three-microRNA signature for lung squamous cell carcinoma diagnosis in Chinese male patients
title_short A three-microRNA signature for lung squamous cell carcinoma diagnosis in Chinese male patients
title_sort three-microrna signature for lung squamous cell carcinoma diagnosis in chinese male patients
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689734/
https://www.ncbi.nlm.nih.gov/pubmed/29156844
http://dx.doi.org/10.18632/oncotarget.19666
work_keys_str_mv AT zhanglan athreemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT shanxia athreemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT wangjun athreemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT zhujun athreemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT huangzebo athreemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT zhanghuo athreemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT zhouxin athreemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT chengwenfang athreemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT shuyongqian athreemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT zhuwei athreemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT liuping athreemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT zhanglan threemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT shanxia threemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT wangjun threemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT zhujun threemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT huangzebo threemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT zhanghuo threemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT zhouxin threemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT chengwenfang threemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT shuyongqian threemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT zhuwei threemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients
AT liuping threemicrornasignatureforlungsquamouscellcarcinomadiagnosisinchinesemalepatients