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Article

Screening of targeted genes in extrahepatic bile ducts of mice with experimental biliary atresia

  • Authors:
    • Zhen You
    • Jing Wen
    • Liping Cheng
    • Hui Ye
    • Bei Li
  • View Affiliations / Copyright

    Affiliations: Department of Biliary Surgery, West China Hospital, Chengdu, Sichuan 610041, P.R. China, Campus Hospital, Sichuan University, Chengdu, Sichuan 610000, P.R. China
  • Pages: 4326-4331
    |
    Published online on: June 9, 2015
       https://doi.org/10.3892/mmr.2015.3903
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Abstract

Biliary atresia (BA) is an infantile disease resulting from a severe cholangiopathy, which can obstruct extrahepatic bile ducts, disrupt bile flow and lead to end‑stage cirrhosis. The current study aimed to develop a genetic method to investigate the pathogenesis of BA. The gene expression profile of BA (GSE46967) was downloaded from the Gene Expression Omnibus database and included 18 samples from newborn mice. These samples were collected at three time points following the induction of BA with rhesus rotavirus. The differentially expressed genes (DEGs) in mice with BA were identified using the limma package in R language, followed by hierarchical clustering analysis. Gene ontology functional analysis and Kyoto Enrichment of Genes and Genomes pathway analysis of the selected common DEGs was conducted using the Database for Annotation, Visualization and Integrated Discovery. In total, 306 DEGs were identified in the samples from the 3 day time point, 721 at 7 days and 370 at 14 days. A total of 74 common DEGs were identified in these three sample groups, which are reported to function in multiple immune biological processes, including the defense response, leukocyte migration, cell chemotaxis and leukocyte chemotaxis. In addition, ‘cytokine‑cytokine receptor interaction’ and ‘chemokine signaling pathway’ were observed to be significantly enriched in BA. A total of six common DEGs (CCL3, CXCL5, CXCL13, CXCR2, CCL5 and CCL6) were identified that were involved in the significantly enriched functions and the significantly enriched pathways. The data from the current study suggested that the immune response is a critical biological process in the development of BA. The six critical hub genes identified (CCL3, CXCL5, CXCL13, CXCR2, CCL5 and CCL6) may be used as specific target genes in the treatment of BA.
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Copy and paste a formatted citation
Spandidos Publications style
You Z, Wen J, Cheng L, Ye H and Li B: Screening of targeted genes in extrahepatic bile ducts of mice with experimental biliary atresia. Mol Med Rep 12: 4326-4331, 2015.
APA
You, Z., Wen, J., Cheng, L., Ye, H., & Li, B. (2015). Screening of targeted genes in extrahepatic bile ducts of mice with experimental biliary atresia. Molecular Medicine Reports, 12, 4326-4331. https://doi.org/10.3892/mmr.2015.3903
MLA
You, Z., Wen, J., Cheng, L., Ye, H., Li, B."Screening of targeted genes in extrahepatic bile ducts of mice with experimental biliary atresia". Molecular Medicine Reports 12.3 (2015): 4326-4331.
Chicago
You, Z., Wen, J., Cheng, L., Ye, H., Li, B."Screening of targeted genes in extrahepatic bile ducts of mice with experimental biliary atresia". Molecular Medicine Reports 12, no. 3 (2015): 4326-4331. https://doi.org/10.3892/mmr.2015.3903
Copy and paste a formatted citation
x
Spandidos Publications style
You Z, Wen J, Cheng L, Ye H and Li B: Screening of targeted genes in extrahepatic bile ducts of mice with experimental biliary atresia. Mol Med Rep 12: 4326-4331, 2015.
APA
You, Z., Wen, J., Cheng, L., Ye, H., & Li, B. (2015). Screening of targeted genes in extrahepatic bile ducts of mice with experimental biliary atresia. Molecular Medicine Reports, 12, 4326-4331. https://doi.org/10.3892/mmr.2015.3903
MLA
You, Z., Wen, J., Cheng, L., Ye, H., Li, B."Screening of targeted genes in extrahepatic bile ducts of mice with experimental biliary atresia". Molecular Medicine Reports 12.3 (2015): 4326-4331.
Chicago
You, Z., Wen, J., Cheng, L., Ye, H., Li, B."Screening of targeted genes in extrahepatic bile ducts of mice with experimental biliary atresia". Molecular Medicine Reports 12, no. 3 (2015): 4326-4331. https://doi.org/10.3892/mmr.2015.3903
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