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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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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:30945310
kind
science-record
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sha256:2d85b12c1f36afb4b3e692c2e16f356946ef98490eeb0d0cd91651c5fb9439ab
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created_at
2026-11-01T15:40:44Z
updated_at
2026-11-01T22:00:28Z
generator object · 2 fields
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paper object · 10 fields
state
complete
title
G Protein γ subunit 7 loss contributes to progression of clear cell renal cell carcinoma.
doi
10.1002/jcp.28597
pmid
30945310
authors array · 6 items
[0]
Shan Xu
[1]
Haibao Zhang
[2]
Tianjie Liu
[3]
Yule Chen
[4]
Dalin He
[5]
Lei Li
journal
Journal of cellular physiology
year
2019
abstract
Clear cell renal cell carcinoma (ccRCC) is a common urinary neoplasm, looking for useful candidates to establish scientific foundation for the therapy of ccRCC is urgent. 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. Further, Gene Set Enrichment Analysis results showed that mTOR1, E2F, G2M, and MYC pathways were all significantly altered in response to GNG7 low expression. In vitro, A498 and 786-O cells in which GNG7 expression was silenced, exhibited a lower G1 phase when compared to the negative control cells. Taken together, our findings suggest that GNG7 is a tumor suppressor gene in ccRCC progression and represents a novel candidate for ccRCC treatment.
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The differences between two groups (Student's t test) were analyzed by GraphPad Prism version 6.0 software (GraphPad), p < 0.05 was considered significant.
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sections[15] "Statistical analysis" paragraph 2
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The differences between two groups (Student's t test) were analyzed by GraphPad Prism version 6.0 software (GraphPad), p < 0.05 was considered significant.
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GSE781, GSE6244, GSE53757, and GSE66271 were applied from the Gene Expression Omnibus (GEO), nine ccRCC patients‐tumor tissue and matched normal tissue were obtained after surgery in GSE781 data set on a GLP96/97 platform (Lenburg et al., 2003);
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sections[3] "Microarray data" paragraph 2
quote
GSE781, GSE6244, GSE53757, and GSE66271 were applied from the Gene Expression Omnibus (GEO), nine ccRCC patients‐tumor tissue and matched normal tissue were obtained after surgery in GSE781 data set on a GLP96/97 platform (Lenburg et al., 2003);
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the published estimate and its evidence
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the source data with its repository provenance
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GSE781, GSE6244, GSE53757, and GSE66271 were applied from the Gene Expression Omnibus (GEO), nine ccRCC patients‐tumor tissue and matched normal tissue were obtained after surgery in GSE781 data set on a GLP96/97 platform (Lenburg et al., 2003);
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GSE781, GSE6244, GSE53757, and GSE66271 were applied from the Gene Expression Omnibus (GEO), nine ccRCC patients‐tumor tissue and matched normal tissue were obtained after surgery in GSE781 data set on a GLP96/97 platform (Lenburg et al., 2003);
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GSM1300180
[119]
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[120]
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GSM1300185
[124]
GSM1300186
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[139]
GSM1300201
[140]
GSM1300202
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GSM1300205
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144
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570
taxon
Homo sapiens
title
Gene array analysis of clear cell renal cell carcinoma tissue versus matched normal kidney tissue
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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[2] object · 15 fields
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GSE781, GSE6244, GSE53757, and GSE66271 were applied from the Gene Expression Omnibus (GEO), nine ccRCC patients‐tumor tissue and matched normal tissue were obtained after surgery in GSE781 data set on a GLP96/97 platform (Lenburg et al., 2003);
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GEO accession URL
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GSE781, GSE6244, GSE53757, and GSE66271 were applied from the Gene Expression Omnibus (GEO), nine ccRCC patients‐tumor tissue and matched normal tissue were obtained after surgery in GSE781 data set on a GLP96/97 platform (Lenburg et al., 2003);
access_statement_kind
repository_route_statement
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GSM143851
[1]
GSM143853
[2]
GSM143855
[3]
GSM143858
[4]
GSM143860
[5]
GSM143861
sample_count
6
group_sizes
null
group_sizes_basis
null
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892
taxon
Oryza sativa Japonica Group; Oryza sativa Indica Group
title
Transcriptional profiling of indica rice cultivar IET8585 (Ajaya) infected with bacterial leaf blight pathogen (Xoo)
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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false
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[3] object · 15 fields
id
data:geo:GSE66271
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raw
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geo-series
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE66271
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null
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null
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null
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GSE781, GSE6244, GSE53757, and GSE66271 were applied from the Gene Expression Omnibus (GEO), nine ccRCC patients‐tumor tissue and matched normal tissue were obtained after surgery in GSE781 data set on a GLP96/97 platform (Lenburg et al., 2003);
structure object · 15 fields
repository
GEO
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GEO accession URL
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GSE781, GSE6244, GSE53757, and GSE66271 were applied from the Gene Expression Omnibus (GEO), nine ccRCC patients‐tumor tissue and matched normal tissue were obtained after surgery in GSE781 data set on a GLP96/97 platform (Lenburg et al., 2003);
access_statement_kind
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[0]
GSM1618415
[1]
GSM1618416
[2]
GSM1618417
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GSM1618438
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GSM1618440
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26
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null
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null
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570
taxon
Homo sapiens
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Genome-wide analysis of gene expression patterns in human kidney cancer [patients with metastasis]
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2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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GSE781, GSE6244, GSE53757, and GSE66271 were applied from the Gene Expression Omnibus (GEO), nine ccRCC patients‐tumor tissue and matched normal tissue were obtained after surgery in GSE781 data set on a GLP96/97 platform (Lenburg et al., 2003);
structure object · 15 fields
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GSE781, GSE6244, GSE53757, and GSE66271 were applied from the Gene Expression Omnibus (GEO), nine ccRCC patients‐tumor tissue and matched normal tissue were obtained after surgery in GSE781 data set on a GLP96/97 platform (Lenburg et al., 2003);
access_statement_kind
repository_route_statement
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[0]
GSM11805
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GSM11810
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GSM12448
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34
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null
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null
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96;97
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Homo sapiens
title
Normal and Renal Cell Carcinoma Kidney Tissue, Human
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Four hub genes with MCC value > 1,000 and degree ≥ 10
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PMC6767067
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17
section_title
The hub genes in clear cell renal cell carcinoma progression
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Table 1
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Four hub genes with MCC value > 1,000 and degree ≥ 10
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[0]
Nos.
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Gene symbol
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Full name
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[0]
1
[1]
GNG2
[2]
G Protein subunit γ 2
[3]
GNG2 inhibits proliferation of malignant melanoma cells in vitro and in vivo
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[0]
2
[1]
GNG7
[2]
G Protein subunit γ 7
[3]
Low‐expression GNG7 is associated with tumor grade and stage
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[0]
3
[1]
KNG1
[2]
Kininogen 1
[3]
Kininogen‐1 is a constituent of the blood coagulation system as well as the kinin‐kallikrein system
[4] array · 4 items
[0]
4
[1]
GNB4
[2]
G protein subunit β 4
[3]
GNB4 mutations as a cause of Dominant Intermediate Charcot‐Marie‐Tooth Disease
locator
section[17]/table-wrap[1]#jcp28597-tbl-0001
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[0]
asset:data:geo:GSE53757 not downloaded
[1]
asset:data:geo:GSE53757 licence not read
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[3]
asset:data:geo:GSE6244 licence not read
[4]
asset:data:geo:GSE66271 not downloaded
[5]
asset:data:geo:GSE66271 licence not read
[6]
asset:data:geo:GSE781 not downloaded
[7]
asset:data:geo:GSE781 licence not read
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The differences between two groups (Student's t test) were analyzed by GraphPad Prism version 6.0 software (GraphPad), p < 0.05 was considered significant.
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[0]
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[6]
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[7]
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[8]
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Automated Assays Laravel application and simulated adapters
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GSE781
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GSE6244
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GSE53757
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[0]
GSE781, GSE6244, GSE53757, and GSE66271 were applied from the Gene Expression Omnibus (GEO), nine ccRCC patients‐tumor tissue and matched normal tissue were obtained after surgery in GSE781 data set on a GLP96/97 platform (Lenburg et al., 2003);
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The paper names GSE781, GSE6244, GSE53757, GSE66271 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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assets array · 3 items
[0]
source:pmid:30945310
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asset:table:pmid:30945310:1
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The differences between two groups (Student's t test) were analyzed by GraphPad Prism version 6.0 software (GraphPad), p < 0.05 was considered significant.
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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. Further, Gene Set Enrichment Analysis results showed that mTOR1, E2F, G2M, and MYC pathways were all significantly altered in response to GNG7 low expression. In vitro, A498 and 786-O cells in which GNG7 expression was silenced, exhibited a lower G1 phase when compared to the negative control cells. 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