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pmid:30945310
G Protein γ subunit 7 loss contributes to progression of clear cell renal cell carcinoma.
Shan Xu · Haibao Zhang · Tianjie Liu · Yule Chen · Dalin He · Lei Li
Journal of cellular physiology · 2019 doi:10.1002/jcp.28597
Paper
complete
Experiment
partial
Data
partial
Analysis
partial
Execution
absent
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Complete file
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We downloaded genomic profiles of GSE781, GSE6244, GSE53757, and GSE66271 from the Gene Expression Omnibus (GEO) database. GEO2R was used to analyze the derivative genes, while hub genes were screened by protein-protein interactions and cytoscape. Further, overall survival, gene methylation, gene mutation, and gene expression were all analyzed using bioinformatics tools. Colony formation and cell-cycle assay were used to detect the biological function of GNG7 in vitro. We found that GNG7 was downregulated in ccRCC tissues and negatively associated with overall survival in ccRCC patients. We also found that promoter methylation and frequent gene mutation were responsible for GNG7 gene suppression. GNG7 low expression was related to upregulation of enhancer of zeste homolog 2 and downregulation of disabled homolog 2-interacting protein. 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