Open Access

Identifying pathway modules of tuberculosis in children by analyzing multiple different networks

  • Authors:
    • Lu Cheng
    • Yuling Han
    • Xiuxia Zhao
    • Xiaoli Xu
    • Jing Wang
  • View Affiliations

  • Published online on: November 2, 2017     https://doi.org/10.3892/etm.2017.5434
  • Pages: 755-760
  • Copyright: © Cheng et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Tuberculosis (TB), which is caused by the mycobacterium TB, is the major cause of human death worldwide. The aim of this study was to identify the biomarkers involved in child TB. Gene expression data were obtained from the Array Express Archive of Functional Genomics Data. Gene expression data and protein-protein interaction (PPI) data were downloaded to construct differential gene co-expression networks (DCNs). The Benjamini-Hochberg algorithm was used to correct the P-value. In total, 3,820 edges (PPIs) and 1,359 nodes (genes) were obtained from the human-related PPIs data and gene expression data at the criteria of absolute value of Pearson's correlation coefficient >0.8. The DCNs were formed by these edges and nodes. Thirteen seed genes were obtained by ranging z-scores. Eight significant multiple different modules were identified from DCNs using the statistical significant test. In conclusion, the seed genes and significant modules constitute potential biomarkers that reveal the underlying mechanisms in child TB. The new identified biomarkers may contribute to an understanding of TB and provide a new therapeutic method for the treatment of TB.
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January-2018
Volume 15 Issue 1

Print ISSN: 1792-0981
Online ISSN:1792-1015

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Copy and paste a formatted citation
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Spandidos Publications style
Cheng L, Han Y, Zhao X, Xu X and Wang J: Identifying pathway modules of tuberculosis in children by analyzing multiple different networks. Exp Ther Med 15: 755-760, 2018
APA
Cheng, L., Han, Y., Zhao, X., Xu, X., & Wang, J. (2018). Identifying pathway modules of tuberculosis in children by analyzing multiple different networks. Experimental and Therapeutic Medicine, 15, 755-760. https://doi.org/10.3892/etm.2017.5434
MLA
Cheng, L., Han, Y., Zhao, X., Xu, X., Wang, J."Identifying pathway modules of tuberculosis in children by analyzing multiple different networks". Experimental and Therapeutic Medicine 15.1 (2018): 755-760.
Chicago
Cheng, L., Han, Y., Zhao, X., Xu, X., Wang, J."Identifying pathway modules of tuberculosis in children by analyzing multiple different networks". Experimental and Therapeutic Medicine 15, no. 1 (2018): 755-760. https://doi.org/10.3892/etm.2017.5434