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Identification of a key candidate gene‑phenotype network mediated by glycyrrhizic acid using pharmacogenomic analysis

  • Authors:
    • Shiqun Wang
    • Lu Li
    • Long Shi
  • View Affiliations / Copyright

    Affiliations: Xiaoshan Biotechnology Center, Yangtze Delta Region Institute of Tsinghua University, Hangzhou, Zhejiang 311231, P.R. China, Department of Nephrology, Affiliated Children's Hospital of Zhejiang University, Hangzhou, Zhejiang 310052, P.R. China
    Copyright: © Wang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 2657-2666
    |
    Published online on: July 12, 2019
       https://doi.org/10.3892/mmr.2019.10494
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Abstract

Glycyrrhizic acid (GA) is primarily used as an anti‑inflammatory agent in cases of chronic hepatitis. However, its underlying mechanisms in diverse biological processes and its reported benefits are yet to be fully elucidated. In the current study, an analytical method based on pharmacogenomics was established to mine disease‑modulatory activities mediated by GA. Five primary protein targets and 138 functional partners were identified for GA by querying open‑source databases, including Drugbank and STRING. Subsequently, GA‑associated primary and secondary protein targets were integrated into Cytoscape to construct a protein‑protein interaction network to establish connectivity. GA‑associated target genes were then clustered based on Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis. The tumor necrosis factor axis was revealed to be a primary module regulated by GA‑associated targets. Furthermore, 12 hub genes were queried to assess their potential anti‑cancer effects using cBioPortal. The results indicated that pharmacogenomics‑based analysis improved understanding of the underlying drug‑target events of GA and provided predictive and definitive leads for future studies.
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Copy and paste a formatted citation
Spandidos Publications style
Wang S, Li L and Shi L: Identification of a key candidate gene‑phenotype network mediated by glycyrrhizic acid using pharmacogenomic analysis. Mol Med Rep 20: 2657-2666, 2019.
APA
Wang, S., Li, L., & Shi, L. (2019). Identification of a key candidate gene‑phenotype network mediated by glycyrrhizic acid using pharmacogenomic analysis. Molecular Medicine Reports, 20, 2657-2666. https://doi.org/10.3892/mmr.2019.10494
MLA
Wang, S., Li, L., Shi, L."Identification of a key candidate gene‑phenotype network mediated by glycyrrhizic acid using pharmacogenomic analysis". Molecular Medicine Reports 20.3 (2019): 2657-2666.
Chicago
Wang, S., Li, L., Shi, L."Identification of a key candidate gene‑phenotype network mediated by glycyrrhizic acid using pharmacogenomic analysis". Molecular Medicine Reports 20, no. 3 (2019): 2657-2666. https://doi.org/10.3892/mmr.2019.10494
Copy and paste a formatted citation
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Spandidos Publications style
Wang S, Li L and Shi L: Identification of a key candidate gene‑phenotype network mediated by glycyrrhizic acid using pharmacogenomic analysis. Mol Med Rep 20: 2657-2666, 2019.
APA
Wang, S., Li, L., & Shi, L. (2019). Identification of a key candidate gene‑phenotype network mediated by glycyrrhizic acid using pharmacogenomic analysis. Molecular Medicine Reports, 20, 2657-2666. https://doi.org/10.3892/mmr.2019.10494
MLA
Wang, S., Li, L., Shi, L."Identification of a key candidate gene‑phenotype network mediated by glycyrrhizic acid using pharmacogenomic analysis". Molecular Medicine Reports 20.3 (2019): 2657-2666.
Chicago
Wang, S., Li, L., Shi, L."Identification of a key candidate gene‑phenotype network mediated by glycyrrhizic acid using pharmacogenomic analysis". Molecular Medicine Reports 20, no. 3 (2019): 2657-2666. https://doi.org/10.3892/mmr.2019.10494
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