Open Access

Construction of protein interaction network involved in lung adenocarcinomas using a novel algorithm

  • Authors:
    • Juan Chen
    • Hai‑Tao Yang
    • Zhu Li
    • Ning Xu
    • Bo Yu
    • Jun‑Ping Xu
    • Pei‑Ge Zhao
    • Yan Wang
    • Xiu‑Juan Zhang
    • Dian‑Jie Lin
  • View Affiliations

  • Published online on: July 7, 2016     https://doi.org/10.3892/ol.2016.4822
  • Pages: 1792-1800
  • Copyright: © Chen et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Studies that only assess differentially‑expressed (DE) genes do not contain the information required to investigate the mechanisms of diseases. A complete knowledge of all the direct and indirect interactions between proteins may act as a significant benchmark in the process of forming a comprehensive description of cellular mechanisms and functions. The results of protein interaction network studies are often inconsistent and are based on various methods. In the present study, a combined network was constructed using selected gene pairs, following the conversion and combination of the scores of gene pairs that were obtained across multiple approaches by a novel algorithm. Samples from patients with and without lung adenocarcinoma were compared, and the RankProd package was used to identify DE genes. The empirical Bayesian (EB) meta‑analysis approach, the search tool for the retrieval of interacting genes/proteins database (STRING), the weighted gene coexpression network analysis (WGCNA) package and the differentially‑coexpressed genes and links package (DCGL) were used for network construction. A combined network was also constructed with a novel rank‑based algorithm using a combined score. The topological features of the 5 networks were analyzed and compared. A total of 941 DE genes were screened. The topological analysis indicated that the gene interaction network constructed using the WGCNA method was more likely to produce a small‑world property, which has a small average shortest path length and a large clustering coefficient, whereas the combined network was confirmed to be a scale‑free network. Gene pairs that were identified using the novel combined method were mostly enriched in the cell cycle and p53 signaling pathway. The present study provided a novel perspective to the network‑based analysis. Each method has advantages and disadvantages. Compared with single methods, the combined algorithm used in the present study may provide a novel method to analyze gene interactions, with increased credibility.

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September-2016
Volume 12 Issue 3

Print ISSN: 1792-1074
Online ISSN:1792-1082

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Copy and paste a formatted citation
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Spandidos Publications style
Chen J, Yang HT, Li Z, Xu N, Yu B, Xu JP, Zhao PG, Wang Y, Zhang XJ, Lin DJ, Lin DJ, et al: Construction of protein interaction network involved in lung adenocarcinomas using a novel algorithm. Oncol Lett 12: 1792-1800, 2016
APA
Chen, J., Yang, H., Li, Z., Xu, N., Yu, B., Xu, J. ... Lin, D. (2016). Construction of protein interaction network involved in lung adenocarcinomas using a novel algorithm. Oncology Letters, 12, 1792-1800. https://doi.org/10.3892/ol.2016.4822
MLA
Chen, J., Yang, H., Li, Z., Xu, N., Yu, B., Xu, J., Zhao, P., Wang, Y., Zhang, X., Lin, D."Construction of protein interaction network involved in lung adenocarcinomas using a novel algorithm". Oncology Letters 12.3 (2016): 1792-1800.
Chicago
Chen, J., Yang, H., Li, Z., Xu, N., Yu, B., Xu, J., Zhao, P., Wang, Y., Zhang, X., Lin, D."Construction of protein interaction network involved in lung adenocarcinomas using a novel algorithm". Oncology Letters 12, no. 3 (2016): 1792-1800. https://doi.org/10.3892/ol.2016.4822