Identification of potential key genes associated with severe pneumonia using mRNA-seq

dc.contributor.authorFeng, Cong
dc.contributor.authorHuang, He
dc.contributor.authorHuang, Sai
dc.contributor.authorZhai, Yong-Zhi
dc.contributor.authorDong, Jing
dc.contributor.authorChen, Li
dc.contributor.authorHuang, Zhi
dc.contributor.authorZhou, Xuan
dc.contributor.authorLi, Bei
dc.contributor.authorWang, Li-Li
dc.contributor.authorChen, Wei
dc.contributor.authorLv, Fa-Qin
dc.contributor.authorLi, Tan-Shi
dc.contributor.departmentElectrical and Computer Engineering, School of Engineering and Technologyen_US
dc.date.accessioned2019-05-10T17:37:38Z
dc.date.available2019-05-10T17:37:38Z
dc.date.issued2018-08
dc.description.abstractThis 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.en_US
dc.identifier.citationFeng, C., Huang, H., Huang, S., Zhai, Y. Z., Dong, J., Chen, L., … Li, T. S. (2018). Identification of potential key genes associated with severe pneumonia using mRNA-seq. Experimental and therapeutic medicine, 16(2), 758–766. doi:10.3892/etm.2018.6262en_US
dc.identifier.urihttps://hdl.handle.net/1805/19235
dc.language.isoen_USen_US
dc.publisherSpandidosen_US
dc.relation.isversionof10.3892/etm.2018.6262en_US
dc.relation.journalExperimental and Therapeutic Medicineen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.sourcePMCen_US
dc.subjectChronic obstructive pulmonary diseaseen_US
dc.subjectCoexpressionen_US
dc.subjectDifferentially expressed geneen_US
dc.subjectNetworken_US
dc.subjectSevere pneumoniaen_US
dc.titleIdentification of potential key genes associated with severe pneumonia using mRNA-seqen_US
dc.typeArticleen_US
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
etm-16-02-0758.pdf
Size:
1.31 MB
Format:
Adobe Portable Document Format
Description:
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.99 KB
Format:
Item-specific license agreed upon to submission
Description: