Open Access

Bioinformatics and functional analyses of key genes and pathways in human clear cell renal cell carcinoma

  • Authors:
    • Jinxing Wang
    • Lushun Yuan
    • Xingnian Liu
    • Gang Wang
    • Yuan Zhu
    • Kaiyu Qian
    • Yu Xiao
    • Xinghuan Wang
  • View Affiliations

  • Published online on: April 12, 2018     https://doi.org/10.3892/ol.2018.8473
  • Pages: 9133-9141
  • Copyright: © Wang 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

Clear cell renal cell carcinoma (ccRCC) is the most common type of kidney cancer. The present study was conducted to explore the mechanisms and identify the potential target genes for ccRCC using bioinformatics analysis. The microarray data of GSE15641 were screened on Gene‑Cloud of Biotechnology Information (GCBI). A total of 32 ccRCC samples and 23 normal kidney samples were used to identify differentially expressed genes (DEGs) between them. Subsequently, the clustering analysis and functional enrichment analysis of these DEGs were performed, followed by protein‑protein interaction (PPI) network, and pathway relation network. Additionally, the most significant module based on PPI network was selected, and the genes in the module were identified as hub genes. Furthermore, transcriptional level, translational level and survival analyses of hub genes were performed to verify the results. A total of 805 genes, 403 upregulated and 402 downregulated, were differentially expressed in ccRCC samples compared with normal controls. The subsequent bioinformatics analysis indicated that the small molecule metabolic process and the metabolic pathway were significantly enriched. A total of 7 genes, including membrane metallo‑endopeptidase (MME), albumin (ALB), cadherin 1 (CDH1), prominin 1 (ROM1), chemokine (C‑X‑C motif) ligand 12 (CXCL12), protein tyrosine phosphatase receptor type C (PTPRC) and intercellular adhesion molecule 1 (ICAM1) were identified as hub genes. In brief, the present study indicated that these candidate genes and pathways may aid in deciphering the molecular mechanisms underlying the development of ccRCC, and may be used as therapeutic targets and diagnostic biomarkers of ccRCC.
View Figures
View References

Related Articles

Journal Cover

June-2018
Volume 15 Issue 6

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

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Wang J, Yuan L, Liu X, Wang G, Zhu Y, Qian K, Xiao Y and Wang X: Bioinformatics and functional analyses of key genes and pathways in human clear cell renal cell carcinoma. Oncol Lett 15: 9133-9141, 2018.
APA
Wang, J., Yuan, L., Liu, X., Wang, G., Zhu, Y., Qian, K. ... Wang, X. (2018). Bioinformatics and functional analyses of key genes and pathways in human clear cell renal cell carcinoma. Oncology Letters, 15, 9133-9141. https://doi.org/10.3892/ol.2018.8473
MLA
Wang, J., Yuan, L., Liu, X., Wang, G., Zhu, Y., Qian, K., Xiao, Y., Wang, X."Bioinformatics and functional analyses of key genes and pathways in human clear cell renal cell carcinoma". Oncology Letters 15.6 (2018): 9133-9141.
Chicago
Wang, J., Yuan, L., Liu, X., Wang, G., Zhu, Y., Qian, K., Xiao, Y., Wang, X."Bioinformatics and functional analyses of key genes and pathways in human clear cell renal cell carcinoma". Oncology Letters 15, no. 6 (2018): 9133-9141. https://doi.org/10.3892/ol.2018.8473