Transcriptome signatures reveal candidate key genes in the whole blood of patients with lumbar disc prolapse

Wang,Yi; Dai,Guogang; Li,Lengtao; Liu,Lijuan; Jiang,Ling; Li,Shengwu; Liao,Shichuan; Wang,Feng; Du,Wanli; Li,Yuewen

doi:10.3892/etm.2019.8137

Transcriptome signatures reveal candidate key genes in the whole blood of patients with lumbar disc prolapse

Authors:
- Yi Wang
- Guogang Dai
- Lengtao Li
- Lijuan Liu
- Ling Jiang
- Shengwu Li
- Shichuan Liao
- Feng Wang
- Wanli Du
- Yuewen Li
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Affiliations: Cervicodynia/Omalgia/Lumbago/Sciatica Department, Sichuan Provincial Orthopedic Hospital, Chengdu, Sichuan 610041, P.R. China, Postgraduate School, Chengdu Sport Institute, Chengdu, Sichuan 610041, P.R. China, College Hospital, Sichuan Agricultural University ‑ Chengdu Campus, Chengdu, Sichuan 611130, P.R. China
Published online on: October 25, 2019 https://doi.org/10.3892/etm.2019.8137
Pages: 4591-4602
Copyright: © Wang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

The present study aimed to investigate differentially expressed genes (DEGs) in whole blood (WB) obtained from patients with lumbar disc prolapse (LDP) and healthy volunteers. A total of 8 patients with LDP and 8 healthy volunteers were recruited. An Agilent SurePrint G3 human gene expression microarray 8x60 K was used to perform the microarray analyses. R was employed to identify DEGs, which were then subjected to bioinformatics analysis, including a Gene Ontology (GO) analysis, Kyoto Encyclopaedia of Genes and Genomes (KEGG) pathway analysis and protein‑protein interaction (PPI) network analysis. DEGs in the degenerative annulus fibrosis (AF) and nucleus pulposus (NP) compared with non‑degenerative tissues were also identified based on microarray data and the intersections of the three were assessed. Furthermore, reverse transcription‑quantitative (RT‑q)PCR was performed to confirm the aberrant expression levels of selected DEGs in the WB of all subjects. A total of 161 DEGs between LDP patients and the healthy controls were identified (128 upregulated and 33 downregulated). These DEGs were enriched in 293 biological process, 36 cellular component and 21 molecular function GO terms, as well as in 24 KEGG pathways. The PPI network contained 4 submodules, and Toll‑like receptor 4 had the highest degree centrality. A total of 22 DEGs were common to the three groups of DEGs. The RT‑qPCR assay confirmed that the expression levels of cytochrome P450 family 27 subfamily A member 1, superoxide dismutase 2, protein disulfide isomerase family A member 4, FKBP prolyl isomerase 11 and ectonucleotide pyrophosphatase/phosphodiesterase 4 were significantly different between the patient group and the volunteer group. In conclusion, several genes were identified as potential biomarkers in WB that should be further explored in future studies to determine their potential application in the clinical treatment and diagnosis of LDP, and the present bioinformatics analysis revealed several GO terms, KEGG pathways and submodules of the PPI network that may be involved in LDP, although the exact mechanisms remain elusive.

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