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Mapping the Structure-Function Relationships of Disordered Oncogenic Transcription Factors Using Transcriptomic Analysis
Published on: June 27, 2020
Transcriptomic analysis reveals the underlying pro-malignant functions of Gankyrin for colorectal cancer via
Baojin Xu1, Shenglong Li2, Wu Lv1
1Department of General Surgery, Cancer Hospital of China Medical University, Liaoning Cancer Hospital and Institute, Shenyang, China.
Background:
Recently increasing evidence had indicated Gankyrin play an important role for the development and progression of colorectal cancer (CRC). However, its function mechanisms remain unclear. The goal of this study was to further illuminate the roles of Gankyrin in CRC using microarray data.
Methods:
The microarray data of CRC was extracted from the Gene Expression Omnibus (GEO) database under the accession number GSE44029. Differentially expressed genes (DEGs) were identified using the LIMMA method, and then protein-protein interaction (PPI) network was constructed to screen crucial genes associated with Gankyrin. GO and KEGG pathway enrichment analysis were performed to investigate the underlying functions of DEGs using DAVID tool.
Results:
A total of 712 genes were identified as DEGs, including 15 upregulated genes and 697 downregulated genes. Go enrichment analysis indicated that Gankyrin was involved in tumor necrosis factor-mediated signaling pathway. A PPI network including 586 nodes and 654 edges was constructed, in which BIRC3 and PSMB9 were demonstrated to be the hub genes associated with Gankyrin.
Conclusion:
Our present study preliminarily revealed that the pro-malignant effects of Gankyrin in CRC cells may be mediated by affecting TNF signaling pathway via changing the expression of the crucial enriched genes (BIRC3 and PSMB9).
Insights
Gankyrin promotes colorectal cancer (CRC) progression, potentially by influencing the tumor necrosis factor (TNF) signaling pathway. This study identified BIRC3 and PSMB9 as key genes involved in Gankyrin
Area of Science:
- Oncology
- Molecular Biology
- Bioinformatics
Background:
- Gankyrin is increasingly implicated in colorectal cancer (CRC) development and progression.
- The precise functional mechanisms of Gankyrin in CRC remain largely unelucidated.
Purpose of the Study:
- To investigate the role of Gankyrin in colorectal cancer using microarray data.
- To identify key genes and pathways associated with Gankyrin function in CRC.
Main Methods:
- Utilized Gene Expression Omnibus (GEO) dataset GSE44029 for CRC microarray data.
- Identified differentially expressed genes (DEGs) using the LIMMA method.
- Constructed a protein-protein interaction (PPI) network and performed Gene Ontology (GO) and KEGG pathway enrichment analysis.
Main Results:
- Identified 712 DEGs (15 upregulated, 697 downregulated) in CRC.
- Gankyrin was found to be involved in the tumor necrosis factor-mediated signaling pathway.
- BIRC3 and PSMB9 emerged as crucial hub genes within the Gankyrin-associated PPI network.
Conclusions:
- Gankyrin's pro-malignant effects in CRC may be mediated through the TNF signaling pathway.
- Altered expression of key genes, specifically BIRC3 and PSMB9, is implicated in Gankyrin's function.
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