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Identification of differentially expressed miRNAs in differentiating benign from malignant pleural effusion

BACKGROUND: Tuberculosis pleural effusion (TPE) and malignant pleural effusion (MPE) are very common clinical complications. Considering the totally different prognosis and clinical treatment of TPE and MPE, the accurate and non-invasive diagnosis are very critical for patients with pleural effusion...

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Autores principales: Bao, Quanlei, Xu, Yaping, Ding, Ming, Chen, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7045593/
https://www.ncbi.nlm.nih.gov/pubmed/32102688
http://dx.doi.org/10.1186/s41065-020-00119-z
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author Bao, Quanlei
Xu, Yaping
Ding, Ming
Chen, Ping
author_facet Bao, Quanlei
Xu, Yaping
Ding, Ming
Chen, Ping
author_sort Bao, Quanlei
collection PubMed
description BACKGROUND: Tuberculosis pleural effusion (TPE) and malignant pleural effusion (MPE) are very common clinical complications. Considering the totally different prognosis and clinical treatment of TPE and MPE, the accurate and non-invasive diagnosis are very critical for patients with pleural effusion to initiate efficient management and treatment. However, effective clinical biomarkers were rarely explored to distinguish benign from MPE. The purpose of this study is to identify potential miRNAs which can probably be used to differentiate malignant pleural effusion from TPE. RESULTS: A total of 23 significantly differentially expressed miRNAs were identified in MPE, with 18 up-expressed and 5 down-expressed. And the target genes of the miRNAs mainly involved in the biology process of nervous system, cancer, immune system and metabolic process etc. Three high confident target genes, AGO4, FGF9 and LEF1 can be regulated by miR-195-5p, miR-182-5p and miR-34a-5p respectively. And these genes participate in the canonical pathway of regulation of the Epithelial-Mesenchymal and the biological functions of apoptosis, growth of tumor and cell proliferation of tumor cell lines. Further, RT-PCR validation results based on 64 collected individuals showed that the expression levels of the three miRNAs were 2–5 times higher in MPE samples, which were consistent with the microarray results. In addition, ROC curve analysis demonstrated that the combination of the three miRNAs can achieve higher AUC of 0.93 (p-value< 0.0001) to differentiate MPE from TPE. CONCLUSIONS: The identified miR-195-5p, miR-182-5p and miR-34a-5p can become potential diagnostic biomarkers for MPE with further evidences.
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spelling pubmed-70455932020-03-11 Identification of differentially expressed miRNAs in differentiating benign from malignant pleural effusion Bao, Quanlei Xu, Yaping Ding, Ming Chen, Ping Hereditas Research BACKGROUND: Tuberculosis pleural effusion (TPE) and malignant pleural effusion (MPE) are very common clinical complications. Considering the totally different prognosis and clinical treatment of TPE and MPE, the accurate and non-invasive diagnosis are very critical for patients with pleural effusion to initiate efficient management and treatment. However, effective clinical biomarkers were rarely explored to distinguish benign from MPE. The purpose of this study is to identify potential miRNAs which can probably be used to differentiate malignant pleural effusion from TPE. RESULTS: A total of 23 significantly differentially expressed miRNAs were identified in MPE, with 18 up-expressed and 5 down-expressed. And the target genes of the miRNAs mainly involved in the biology process of nervous system, cancer, immune system and metabolic process etc. Three high confident target genes, AGO4, FGF9 and LEF1 can be regulated by miR-195-5p, miR-182-5p and miR-34a-5p respectively. And these genes participate in the canonical pathway of regulation of the Epithelial-Mesenchymal and the biological functions of apoptosis, growth of tumor and cell proliferation of tumor cell lines. Further, RT-PCR validation results based on 64 collected individuals showed that the expression levels of the three miRNAs were 2–5 times higher in MPE samples, which were consistent with the microarray results. In addition, ROC curve analysis demonstrated that the combination of the three miRNAs can achieve higher AUC of 0.93 (p-value< 0.0001) to differentiate MPE from TPE. CONCLUSIONS: The identified miR-195-5p, miR-182-5p and miR-34a-5p can become potential diagnostic biomarkers for MPE with further evidences. BioMed Central 2020-02-26 /pmc/articles/PMC7045593/ /pubmed/32102688 http://dx.doi.org/10.1186/s41065-020-00119-z Text en © The Author(s) 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Bao, Quanlei
Xu, Yaping
Ding, Ming
Chen, Ping
Identification of differentially expressed miRNAs in differentiating benign from malignant pleural effusion
title Identification of differentially expressed miRNAs in differentiating benign from malignant pleural effusion
title_full Identification of differentially expressed miRNAs in differentiating benign from malignant pleural effusion
title_fullStr Identification of differentially expressed miRNAs in differentiating benign from malignant pleural effusion
title_full_unstemmed Identification of differentially expressed miRNAs in differentiating benign from malignant pleural effusion
title_short Identification of differentially expressed miRNAs in differentiating benign from malignant pleural effusion
title_sort identification of differentially expressed mirnas in differentiating benign from malignant pleural effusion
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7045593/
https://www.ncbi.nlm.nih.gov/pubmed/32102688
http://dx.doi.org/10.1186/s41065-020-00119-z
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