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Identification of potential key genes associated with severe pneumonia using mRNA-seq
This study aimed to identify the potential key genes associated with severe pneumonia using mRNA-seq. Nine peripheral blood samples from patients with severe pneumonia alone (SP group, n=3) and severe pneumonia accompanied with chronic obstructive pulmonary disease (COPD; CSP group, n=3), as well as...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090384/ https://www.ncbi.nlm.nih.gov/pubmed/30112034 http://dx.doi.org/10.3892/etm.2018.6262 |
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author | Feng, Cong Huang, He Huang, Sai Zhai, Yong-Zhi Dong, Jing Chen, Li Huang, Zhi Zhou, Xuan Li, Bei Wang, Li-Li Chen, Wei Lv, Fa-Qin Li, Tan-Shi |
author_facet | Feng, Cong Huang, He Huang, Sai Zhai, Yong-Zhi Dong, Jing Chen, Li Huang, Zhi Zhou, Xuan Li, Bei Wang, Li-Li Chen, Wei Lv, Fa-Qin Li, Tan-Shi |
author_sort | Feng, Cong |
collection | PubMed |
description | This study aimed to identify the potential key genes associated with severe pneumonia using mRNA-seq. Nine peripheral blood samples from patients with severe pneumonia alone (SP group, n=3) and severe pneumonia accompanied with chronic obstructive pulmonary disease (COPD; CSP group, n=3), as well as volunteers without pneumonia (control group, n=3) underwent mRNA-seq. Based on the sequencing data, differentially expressed genes (DEGs) were identified by Limma package. Following the pathway enrichment analysis of DEGs, the genes that were differentially expressed in the SP and CSP groups were selected for pathway enrichment analysis and coexpression analysis. In addition, potential genes related to pneumonia were identified based on the information in the Comparative Toxicogenomics Database. In total, 645 and 528 DEGs were identified in the SP and CSP groups, respectively, compared with the normal controls. Among these DEGs, 88 upregulated genes and 80 downregulated genes were common between the two groups. The functions of the common DEGs were similar to those of the DEGs in the SP group. In the coexpression network, the commonly downregulated genes (including ND1, ND3, ND4L, and ND6) and the commonly upregulated genes (including TSPY6P and CDY10P) exhibited a higher degree. In addition, 131 DEGs (including ND1, ND3, ND6, MIR449A and TAS2R43) were predicted to be potential pneumonia-related genes. In conclusion, the present study demonstrated that the common DEGs may be associated with the progression of severe pneumonia. |
format | Online Article Text |
id | pubmed-6090384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-60903842018-08-15 Identification of potential key genes associated with severe pneumonia using mRNA-seq Feng, Cong Huang, He Huang, Sai Zhai, Yong-Zhi Dong, Jing Chen, Li Huang, Zhi Zhou, Xuan Li, Bei Wang, Li-Li Chen, Wei Lv, Fa-Qin Li, Tan-Shi Exp Ther Med Articles This study aimed to identify the potential key genes associated with severe pneumonia using mRNA-seq. Nine peripheral blood samples from patients with severe pneumonia alone (SP group, n=3) and severe pneumonia accompanied with chronic obstructive pulmonary disease (COPD; CSP group, n=3), as well as volunteers without pneumonia (control group, n=3) underwent mRNA-seq. Based on the sequencing data, differentially expressed genes (DEGs) were identified by Limma package. Following the pathway enrichment analysis of DEGs, the genes that were differentially expressed in the SP and CSP groups were selected for pathway enrichment analysis and coexpression analysis. In addition, potential genes related to pneumonia were identified based on the information in the Comparative Toxicogenomics Database. In total, 645 and 528 DEGs were identified in the SP and CSP groups, respectively, compared with the normal controls. Among these DEGs, 88 upregulated genes and 80 downregulated genes were common between the two groups. The functions of the common DEGs were similar to those of the DEGs in the SP group. In the coexpression network, the commonly downregulated genes (including ND1, ND3, ND4L, and ND6) and the commonly upregulated genes (including TSPY6P and CDY10P) exhibited a higher degree. In addition, 131 DEGs (including ND1, ND3, ND6, MIR449A and TAS2R43) were predicted to be potential pneumonia-related genes. In conclusion, the present study demonstrated that the common DEGs may be associated with the progression of severe pneumonia. D.A. Spandidos 2018-08 2018-06-07 /pmc/articles/PMC6090384/ /pubmed/30112034 http://dx.doi.org/10.3892/etm.2018.6262 Text en Copyright: © Feng 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 Feng, Cong Huang, He Huang, Sai Zhai, Yong-Zhi Dong, Jing Chen, Li Huang, Zhi Zhou, Xuan Li, Bei Wang, Li-Li Chen, Wei Lv, Fa-Qin Li, Tan-Shi Identification of potential key genes associated with severe pneumonia using mRNA-seq |
title | Identification of potential key genes associated with severe pneumonia using mRNA-seq |
title_full | Identification of potential key genes associated with severe pneumonia using mRNA-seq |
title_fullStr | Identification of potential key genes associated with severe pneumonia using mRNA-seq |
title_full_unstemmed | Identification of potential key genes associated with severe pneumonia using mRNA-seq |
title_short | Identification of potential key genes associated with severe pneumonia using mRNA-seq |
title_sort | identification of potential key genes associated with severe pneumonia using mrna-seq |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090384/ https://www.ncbi.nlm.nih.gov/pubmed/30112034 http://dx.doi.org/10.3892/etm.2018.6262 |
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