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Bioinformatics and functional analyses of key genes and pathways in human clear cell renal cell carcinoma
Jinxing Wang1, Lushun Yuan1, Xingnian Liu1
1Department of Urology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, P.R. China.
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.
Insights
Bioinformatics analysis identified 7 key genes, including MME and ALB, as potential therapeutic targets and diagnostic biomarkers for clear cell renal cell carcinoma (ccRCC), offering insights into kidney cancer mechanisms.
Area of Science:
- Oncology
- Bioinformatics
- Molecular Biology
Background:
- Clear cell renal cell carcinoma (ccRCC) is the predominant form of kidney cancer.
- Understanding the molecular mechanisms driving ccRCC is crucial for developing effective treatments.
Purpose of the Study:
- To identify potential therapeutic targets and diagnostic biomarkers for ccRCC.
- To explore the underlying molecular mechanisms of ccRCC using bioinformatics analysis.
Main Methods:
- Screening of microarray data (GSE15641) from ccRCC and normal kidney samples.
- Identification of differentially expressed genes (DEGs), followed by clustering and functional enrichment analysis.
- Construction of protein-protein interaction (PPI) and pathway relation networks to identify hub genes.
Main Results:
- 805 differentially expressed genes (403 upregulated, 402 downregulated) were identified between ccRCC and normal samples.
- Enrichment analysis highlighted significant involvement of small molecule metabolic processes and metabolic pathways.
- Seven hub genes, including MME, ALB, CDH1, ROM1, CXCL12, PTPRC, and ICAM1, were identified.
Conclusions:
- The identified hub genes and enriched pathways provide insights into ccRCC molecular pathogenesis.
- These candidate genes and pathways hold potential as therapeutic targets and diagnostic biomarkers for ccRCC.
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