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Identification of a Combined RNA Prognostic Signature in Adenocarcinoma of the Lung

BACKGROUND: Adenocarcinoma of the lung is a type of non-small cell lung cancer (NSCLC). Clinical outcome is associated with tumor grade, stage, and subtype. This study aimed to identify RNA expression profiles, including long noncoding RNA (lncRNA), microRNA (miRNA), and mRNA, associated with clinic...

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Autores principales: He, Si-Yu, Xi, Wen-Jing, Wang, Xin, Xu, Chao-Han, Cheng, Liang, Liu, Si-Yao, Meng, Qian-Qian, Li, Boyan, Wang, Yahui, Shi, Hong-Bo, Wang, Hong-Jiu, Wang, Zhen-Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556069/
https://www.ncbi.nlm.nih.gov/pubmed/31132294
http://dx.doi.org/10.12659/MSM.913727
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author He, Si-Yu
Xi, Wen-Jing
Wang, Xin
Xu, Chao-Han
Cheng, Liang
Liu, Si-Yao
Meng, Qian-Qian
Li, Boyan
Wang, Yahui
Shi, Hong-Bo
Wang, Hong-Jiu
Wang, Zhen-Zhen
author_facet He, Si-Yu
Xi, Wen-Jing
Wang, Xin
Xu, Chao-Han
Cheng, Liang
Liu, Si-Yao
Meng, Qian-Qian
Li, Boyan
Wang, Yahui
Shi, Hong-Bo
Wang, Hong-Jiu
Wang, Zhen-Zhen
author_sort He, Si-Yu
collection PubMed
description BACKGROUND: Adenocarcinoma of the lung is a type of non-small cell lung cancer (NSCLC). Clinical outcome is associated with tumor grade, stage, and subtype. This study aimed to identify RNA expression profiles, including long noncoding RNA (lncRNA), microRNA (miRNA), and mRNA, associated with clinical outcome in adenocarcinoma of the lung using bioinformatics data. MATERIAL/METHODS: The miRNA and mRNA expression profiles were downloaded from The Cancer Genome Atlas (TCGA) database, and lncRNA expression profiles were downloaded from The Atlas of Noncoding RNAs in Cancer (TANRIC) database. The independent dataset, the Gene Expression Omnibus (GEO) accession dataset, GSE81089, was used. RNA expression profiles were used to identify comprehensive prognostic RNA signatures based on patient survival time. RESULTS: From 7,704 lncRNAs, 787 miRNAs, and 28,937 mRNAs of 449 patients, four joint RNA molecular signatures were identified, including RP11-909N17.2, RP11-14N7.2 (lncRNAs), MIR139 (miRNA), KLHDC8B (mRNA). The random forest (RF) classifier was used to test the prediction ability of patient survival risk and showed a good predictive accuracy of 71% and also showed a significant difference in overall survival (log-rank P=0.0002; HR, 3.54; 95% CI, 1.74–7.19). The combined RNA signature also showed good performance in the identification of patient survival in the validation and independent datasets. CONCLUSIONS: This study identified four RNA sequences as a prognostic molecular signature in adenocarcinoma of the lung, which may also provide an increased understanding of the molecular mechanisms underlying the pathogenesis of this malignancy.
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spelling pubmed-65560692019-06-19 Identification of a Combined RNA Prognostic Signature in Adenocarcinoma of the Lung He, Si-Yu Xi, Wen-Jing Wang, Xin Xu, Chao-Han Cheng, Liang Liu, Si-Yao Meng, Qian-Qian Li, Boyan Wang, Yahui Shi, Hong-Bo Wang, Hong-Jiu Wang, Zhen-Zhen Med Sci Monit Clinical Research BACKGROUND: Adenocarcinoma of the lung is a type of non-small cell lung cancer (NSCLC). Clinical outcome is associated with tumor grade, stage, and subtype. This study aimed to identify RNA expression profiles, including long noncoding RNA (lncRNA), microRNA (miRNA), and mRNA, associated with clinical outcome in adenocarcinoma of the lung using bioinformatics data. MATERIAL/METHODS: The miRNA and mRNA expression profiles were downloaded from The Cancer Genome Atlas (TCGA) database, and lncRNA expression profiles were downloaded from The Atlas of Noncoding RNAs in Cancer (TANRIC) database. The independent dataset, the Gene Expression Omnibus (GEO) accession dataset, GSE81089, was used. RNA expression profiles were used to identify comprehensive prognostic RNA signatures based on patient survival time. RESULTS: From 7,704 lncRNAs, 787 miRNAs, and 28,937 mRNAs of 449 patients, four joint RNA molecular signatures were identified, including RP11-909N17.2, RP11-14N7.2 (lncRNAs), MIR139 (miRNA), KLHDC8B (mRNA). The random forest (RF) classifier was used to test the prediction ability of patient survival risk and showed a good predictive accuracy of 71% and also showed a significant difference in overall survival (log-rank P=0.0002; HR, 3.54; 95% CI, 1.74–7.19). The combined RNA signature also showed good performance in the identification of patient survival in the validation and independent datasets. CONCLUSIONS: This study identified four RNA sequences as a prognostic molecular signature in adenocarcinoma of the lung, which may also provide an increased understanding of the molecular mechanisms underlying the pathogenesis of this malignancy. International Scientific Literature, Inc. 2019-05-27 /pmc/articles/PMC6556069/ /pubmed/31132294 http://dx.doi.org/10.12659/MSM.913727 Text en © Med Sci Monit, 2019 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Clinical Research
He, Si-Yu
Xi, Wen-Jing
Wang, Xin
Xu, Chao-Han
Cheng, Liang
Liu, Si-Yao
Meng, Qian-Qian
Li, Boyan
Wang, Yahui
Shi, Hong-Bo
Wang, Hong-Jiu
Wang, Zhen-Zhen
Identification of a Combined RNA Prognostic Signature in Adenocarcinoma of the Lung
title Identification of a Combined RNA Prognostic Signature in Adenocarcinoma of the Lung
title_full Identification of a Combined RNA Prognostic Signature in Adenocarcinoma of the Lung
title_fullStr Identification of a Combined RNA Prognostic Signature in Adenocarcinoma of the Lung
title_full_unstemmed Identification of a Combined RNA Prognostic Signature in Adenocarcinoma of the Lung
title_short Identification of a Combined RNA Prognostic Signature in Adenocarcinoma of the Lung
title_sort identification of a combined rna prognostic signature in adenocarcinoma of the lung
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556069/
https://www.ncbi.nlm.nih.gov/pubmed/31132294
http://dx.doi.org/10.12659/MSM.913727
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