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pmid:39280680
Identification and expression of prognostic-related genes in kidney renal clear cell carcinoma and their possible regulatory mechanisms.
Qian Liu · Jun Ding
Translational andrology and urology · 2024 doi:10.21037/tau-24-299
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Experiment
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Analysis
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Complete file
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Therefore, a method needs to be developed to diagnose KIRC early, predict patient prognosis, and improve personalized treatments. The objective of this study is to utilize bioinformatics tools and public database resources to identify differentially expressed genes (DEGs) between renal cancer tissues and adjacent normal tissues, and to further screen for prognostic-related genes (PRGs) of KIRC.\nMethods: KIRC was studied using R language and FunRich software and several databases, including the Gene Expression Omnibus (GEO), The Cancer Genome Atlas (TCGA), the University of Alabama at Birmingham cancer data analysis Portal (UALCAN), and Tumor Immune Estimation Resource (TIMER) databases. Moreover, quantitative real-time polymerase chain reaction (qRT-PCR) was used to validate the expression of multiple genes in KIRC and adjacent normal tissues.\nResults: There were substantial differences in immune cell infiltration between the KIRC and adjacent normal tissues in the GSE40435 and GSE46699 datasets. In addition, we screened multiple PRGs of KIRC by combining the GEO and TCGA data. The UALCAN database verified that some representative PRGs were differently expressed depending on the lymph node metastasis status, grade, and stage of KIRC. The qRT-PCR results confirmed the expression of the PRGs in KIRC and adjacent normal tissues. Through the GO and KEGG analyses, interaction analysis, and TIMER database, we found that the prognosis of KIRC was closely related to immune microenvironment and vascular endothelial growth factor (VEGF)/VEGF receptor (VEGFR) signaling.\nConclusions: Our findings could contribute to the prognosis prediction of KIRC, the selection of personalized treatments, and the early diagnosis of KIRC.", "claims": [{"id": "claim-method", "statement": "Differential expression between KIRC tissues and adjacent normal tissues was analyzed using the “limma” package, with significant genes identified at a P value <0.05 and an absolute logFC >1. CIBERSORT was used to assess immune cell infiltration. Pearson correlation analysis was applied to explore relationships between PRGs and TFs. Gene Ontology and KEGG pathway analyses were performed using “clusterProfiler”. 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