Open Access

Identification of potential gene targets in systemic vasculitis using DNA microarray analysis

  • Authors:
    • Yiwen Feng
    • Miao Zheng
    • Shujie Gan
    • Lei Zhang
    • Zhong Wan
    • Yanping Zhang
    • Qin Qian
    • Jingdong Tang
  • View Affiliations

  • Published online on: April 11, 2017     https://doi.org/10.3892/mmr.2017.6455
  • Pages: 3665-3673
  • Copyright: © Feng et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

The present study aimed to identify the involvement of critical genes in systemic vasculitis, to gain an improved understanding of the molecular circuity and to investigate novel potential gene targets for systemic vasculitis treatment. The dual‑color cDNA microarray data of GSE16945, consisting of peripheral mononuclear blood cell specimens from 13 patients with systemic vasculitis and 16 healthy controls, was downloaded from the Gene Expression Omnibus database. Differentially expressed genes (DEGs) were screened in systemic vasculitis compared with controls using BRB ArrayTools, followed by the construction of a protein‑protein interaction (PPI) network using the clusterProfiler package, and significant functional interaction (FI) module selection. Furthermore, transcriptional factors (TFs) among the identified DEGs were predicted and a transcriptional regulation network was constructed. A total of 173 up- and 93 downregulated genes were identified, which were mainly associated with immune response pathways. FBJ murine osteosarcoma viral oncogene homolog (FOS), ubiquitin B (UBB), signal transducer and activator of transcription 1 (STAT1) and MX dynamin‑like GTPase 1 (MX1) were identified as hub proteins in the PPI network. Furthermore, UBB, FOS, and STAT1 were hub proteins in the three identified FI modules, respectively. In total, nine TFs were predicted among the DEGs. Of the DEGs that were predicted to be TFs, STAT1, v‑maf avian musculoaponeurotic fibrosarcoma oncogene homolog B (MAFB) and tyrosine 3‑monooxygenase/tryptophan 5‑monooxygenase activation protein Z (YWHAZ), which interacted with each other, were identified to regulate further DEGs as target genes. Various genes, including FOS, UBB, MX1, STAT1, MAFB, and YWHAZ may be potential targets useful for the treatment of systemic vasculitis.
View Figures
View References

Related Articles

Journal Cover

June-2017
Volume 15 Issue 6

Print ISSN: 1791-2997
Online ISSN:1791-3004

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Feng Y, Zheng M, Gan S, Zhang L, Wan Z, Zhang Y, Qian Q and Tang J: Identification of potential gene targets in systemic vasculitis using DNA microarray analysis. Mol Med Rep 15: 3665-3673, 2017
APA
Feng, Y., Zheng, M., Gan, S., Zhang, L., Wan, Z., Zhang, Y. ... Tang, J. (2017). Identification of potential gene targets in systemic vasculitis using DNA microarray analysis. Molecular Medicine Reports, 15, 3665-3673. https://doi.org/10.3892/mmr.2017.6455
MLA
Feng, Y., Zheng, M., Gan, S., Zhang, L., Wan, Z., Zhang, Y., Qian, Q., Tang, J."Identification of potential gene targets in systemic vasculitis using DNA microarray analysis". Molecular Medicine Reports 15.6 (2017): 3665-3673.
Chicago
Feng, Y., Zheng, M., Gan, S., Zhang, L., Wan, Z., Zhang, Y., Qian, Q., Tang, J."Identification of potential gene targets in systemic vasculitis using DNA microarray analysis". Molecular Medicine Reports 15, no. 6 (2017): 3665-3673. https://doi.org/10.3892/mmr.2017.6455