Identification of crucial genes through WGCNA in the progression of clear cell renal cell carcinoma DOI Creative Commons
Ge Li,

J. M. Wang,

Qiaofei Liu

и другие.

Research Square (Research Square), Год журнала: 2024, Номер unknown

Опубликована: Ноя. 18, 2024

Abstract Background Due to the limited clinical treatment options for clear cell renal carcinoma (ccRCC), this study aimed explore molecular mechanisms underlying ccRCC and identify potential therapeutic targets. Methods A series of bioinformatics techniques were utilized. Differentially expressed genes identified from Gene Expression Omnibus (GEO) dataset. Weighted gene co-expression network analysis (WGCNA) was employed isolate relevant modules. Least absolute shrinkage selection operator regression applied determine target genes, which subsequently validated in The Cancer Genome Atlas Program (TCGA) Multivariate Cox proportional hazards model conducted. Ontology Kyoto Encyclopedia Genes Genomes enrichment analyses performed on intersection genes. relationship between immune cells explored. Dual verification using GEO TCGA data carried out screen Results WGCNA utilized This led discovery 236 differentially 193 candidate hub 12 AIF1L showed statistical differences, with higher expression some samples. Enrichment revealed these genes' implications tumors. Twelve ccRCC-related identified, having diagnostic value correlations cells. Through dual verification, five screened had unique characteristics. Clinical correlation suggested it might act as a suppressor gene. Differences tumor microenvironment observed high- low-expression groups. Conclusion presented notable findings. combination different datasets offered comprehensive understanding promise. finding provides foundation direction future research ccRCC's strategies.

Язык: Английский

Identification of crucial genes through WGCNA in the progression of clear cell renal cell carcinoma DOI Creative Commons
Ge Li,

J. M. Wang,

Qiaofei Liu

и другие.

Research Square (Research Square), Год журнала: 2024, Номер unknown

Опубликована: Ноя. 18, 2024

Abstract Background Due to the limited clinical treatment options for clear cell renal carcinoma (ccRCC), this study aimed explore molecular mechanisms underlying ccRCC and identify potential therapeutic targets. Methods A series of bioinformatics techniques were utilized. Differentially expressed genes identified from Gene Expression Omnibus (GEO) dataset. Weighted gene co-expression network analysis (WGCNA) was employed isolate relevant modules. Least absolute shrinkage selection operator regression applied determine target genes, which subsequently validated in The Cancer Genome Atlas Program (TCGA) Multivariate Cox proportional hazards model conducted. Ontology Kyoto Encyclopedia Genes Genomes enrichment analyses performed on intersection genes. relationship between immune cells explored. Dual verification using GEO TCGA data carried out screen Results WGCNA utilized This led discovery 236 differentially 193 candidate hub 12 AIF1L showed statistical differences, with higher expression some samples. Enrichment revealed these genes' implications tumors. Twelve ccRCC-related identified, having diagnostic value correlations cells. Through dual verification, five screened had unique characteristics. Clinical correlation suggested it might act as a suppressor gene. Differences tumor microenvironment observed high- low-expression groups. Conclusion presented notable findings. combination different datasets offered comprehensive understanding promise. finding provides foundation direction future research ccRCC's strategies.

Язык: Английский

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