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pmid:35984176

Identification of G6PC as a potential prognostic biomarker in hepatocellular carcinoma based on bioinformatics analysis.

Li Tian · Yong Liao

Medicine · 2022 doi:10.1097/MD.0000000000029548

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Experiment

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Data

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Identification of G6PC as a potential prognostic biomarker in hepatocellular carcinoma based on bioinformatics analysis.
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10.1097/MD.0000000000029548
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Li Tian
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Yong Liao
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Medicine
year
2022
abstract
Hepatocellular carcinoma (HCC) has high mortality and incidence rates around the world with limited therapeutic options. There is an urgent need for identification of novel therapeutic targets and biomarkers for early diagnosis and predicting patient survival with HCC. Several studies (GSE102083, GSE29722, GSE101685, and GSE112790) from the GEO database in HCC were screened and analyzed by GEO2R, gene ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis were conducted with the Database for Annotation, Visualization and Integrated Discovery. The protein-protein interaction network was plotted and the module analysis was performed using Search Tool for the Retrieval of Inter-acting Genes/Proteins database and Cytoscape. The expression and survival of key genes were identified using UALCAN, Kaplan-Meier Plotter and ONCOMINE online databases, and the immune infiltration level of key genes was analyzed via the Tumor Immune Estimation Resource (TIMER) database. Through database analysis, eight key genes were finally screened out, and the expressions of cyclin-dependent kinase regulatory subunit 2 and glucose-6-phosphatase catalytic (G6PC), which were closely related to the survival of HCC patients, was detected by using UALCAN. Further analysis on the differential expression of G6PC in multiple cancerous tumors and normal tissues revealed low expression in many solid tumors by Oncomine and TIMER. In addition, Kaplan-Meier plotter and UALCAN database analysis to access diseases prognosis suggested that low expression of G6PC was significantly associated with poor overall survival in HCC patients. Finally, TIMER database analysis showed a significant negative correlation between G6PC and infiltration levels of six kinds of immune cells. The somatic copy number alterations of G6PC were associated with B cells, CD8+ T cells, CD4+ T cells, macrophages, dentritic cells and neutrophils. These bioinformatic data identified G6PC as a potential key gene in the diagnosis and prognosis of HCC.
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GEO2R (https://www.ncbi.nlm.nih.gov/geo/geo2r/)[21] can help us to analyze DEGs, which is an useful online software. Setting adjusted P < .05 and LogFC (Fold Change) > 1.5 or <−1.5 to define DEGs.
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GEO2R (https://www.ncbi.nlm.nih.gov/geo/geo2r/)[21] can help us to analyze DEGs, which is an useful online software. Setting adjusted P < .05 and LogFC (Fold Change) > 1.5 or <−1.5 to define DEGs.
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Data sharing not applicable to this article as no datasets were generated or analyzed during the current study.The datasets generated during and/or analyzed during the current study are publicly available. Gene Expression Omnibus: https://www.ncbi.nlm.nih.gov/geo/
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Data sharing not applicable to this article as no datasets were generated or analyzed during the current study.The datasets generated during and/or analyzed during the current study are publicly available. Gene Expression Omnibus: https://www.ncbi.nlm.nih.gov/geo/
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GEO2R analysis of four GEO microarray datasets yielded 337 common differentially expressed genes.
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Several studies (GSE102083, GSE29722, GSE101685, and GSE112790) from the GEO database in HCC were screened and analyzed by GEO2R, gene ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis were conducted with the Database for Annotation, Visualization and Integrated Discovery.
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sections[10] "3.1. Screening and identification of DEGs in HCC" paragraph 2
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A sum of 337 common DEGs (Fig. 1A) was found in all four datasets, consisting of 126 upregulated genes (Fig. 1B) and 211 down-regulated genes (Fig. 1C).
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GEO2R analysis of four GEO microarray datasets yielded 337 common differentially expressed genes.
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GSM3083620
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GSM3083621
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GSM3083641
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GSM3083642
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[146]
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[147]
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GSM3083660
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GSM3083661
[150]
GSM3083662
[151]
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[152]
GSM3083664
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GSM3083665
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GSM3083668
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GSM3083709
sample_count
198
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Comprehensive molecular characterization of liver cancer and inheritance of the phenotypic traits during tumor recurrence [tissue]
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[4] object · 15 fields
id
data:geo:GSE29722
role
raw
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geo-series
media_type
application/vnd.ncbi.geo-series+json
uri
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE29722
sha256
null
bytes
null
access
open
state
resolved
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null
reader_status
reader_required
identifier
GSE29722
version
null
note
Data sharing not applicable to this article as no datasets were generated or analyzed during the current study.The datasets generated during and/or analyzed during the current study are publicly available. Gene Expression Omnibus: https://www.ncbi.nlm.nih.gov/geo/
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
Data sharing not applicable to this article as no datasets were generated or analyzed during the current study.The datasets generated during and/or analyzed during the current study are publicly available. Gene Expression Omnibus: https://www.ncbi.nlm.nih.gov/geo/
access_statement_kind
data_availability_statement
sample_accessions array · 50 items
[0]
GSM737035
[1]
GSM737036
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GSM737037
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GSM737038
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GSM737039
[5]
GSM737040
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GSM737041
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GSM737042
[8]
GSM737043
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GSM737044
[10]
GSM737045
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GSM737046
[12]
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GSM737048
[14]
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[15]
GSM737050
[16]
GSM737051
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GSM737052
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GSM737053
[19]
GSM737054
[20]
GSM737055
[21]
GSM737056
[22]
GSM737057
[23]
GSM737058
[24]
GSM737059
[25]
GSM737060
[26]
GSM737061
[27]
GSM737062
[28]
GSM737063
[29]
GSM737064
[30]
GSM737065
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GSM737066
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GSM737067
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GSM737068
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GSM737069
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GSM737070
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GSM737071
[37]
GSM737072
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GSM737073
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GSM737074
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GSM737075
[41]
GSM737076
[42]
GSM737077
[43]
GSM737078
[44]
GSM737079
[45]
GSM737080
[46]
GSM737081
[47]
GSM737082
[48]
GSM737083
[49]
GSM737084
sample_count
50
group_sizes
null
group_sizes_basis
null
platform
13685;570
taxon
Homo sapiens
title
The landscape of promoter DNA hypomethylation in liver cancer
resolution_checked_at
2026-11-01T18:06:43Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 8 items
[0]
asset:data:geo:GSE101685 not downloaded
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asset:data:geo:GSE101685 licence not read
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asset:data:geo:GSE102083 not downloaded
[3]
asset:data:geo:GSE102083 licence not read
[4]
asset:data:geo:GSE112790 not downloaded
[5]
asset:data:geo:GSE112790 licence not read
[6]
asset:data:geo:GSE29722 not downloaded
[7]
asset:data:geo:GSE29722 licence not read
analysis object · 4 fields
state
partial
methods array · 5 items
[0] object · 10 fields
id
method-1
family
survival_analysis
specific
kaplan_meier
label
Survival analysis
dsl_operations array · 1 item
[0]
survival_km
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
0.7
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medium
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Kaplan-Meier
[1] object · 10 fields
id
method-2
family
survival_analysis
specific
log_rank_test
label
Survival analysis
dsl_operations array · 1 item
[0]
logrank_test
missing_operations array · 0 items
parameters object · 1 field
p_value
e threshold was logrank P value <
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
0.8
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high
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logrank
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id
method-3
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network_analysis
specific
ppi_network
label
Network / pathway analysis
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[0]
build_graph
[1]
centrality_scores
[2]
pathway_enrich
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
edge_list
evidence object · 3 fields
score
0.7
band
medium
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protein-protein interaction
[3] object · 10 fields
id
method-4
family
network_analysis
specific
pathway_enrichment
label
Network / pathway analysis
dsl_operations array · 1 item
[0]
pathway_enrich
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
edge_list
evidence object · 3 fields
score
0.8
band
high
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pathway enrichment
[4] object · 10 fields
id
method-5
family
null
specific
null
label
GEO2R with adjusted P < .05 and LogFC > 1.5 or <−1.5
dsl_operations array · 0 items
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 0 items
evidence object · 3 fields
score
1
band
verbatim
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GEO2R (https://www.ncbi.nlm.nih.gov/geo/geo2r/)[21] can help us to analyze DEGs, which is an useful online software. Setting adjusted P < .05 and LogFC (Fold Change) > 1.5 or <−1.5 to define DEGs.
targets array · 0 items
gaps array · 1 item
[0]
method.reader_named_unmapped
capability object · 3 fields
state
complete
requirements array · 1 item
[0] object · 6 fields
capability_id
capability:computational_analysis
label
Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
complete
tier
R1
blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
R1
expressible
true
required_operations array · 1 item
[0]
survival_km
missing_operations array · 0 items
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: kaplan_meier.
capability object · 4 fields
tier
R1
capability_id
capability:computational_analysis
availability_state
owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R1
reachable
true
accessions array · 4 items
[0]
GSE102083
[1]
GSE29722
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GSE101685
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GSE112790
resolved_accessions array · 4 items
[0]
GSE102083
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GSE29722
[2]
GSE101685
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GSE112790
statements array · 1 item
[0]
Data sharing not applicable to this article as no datasets were generated or analyzed during the current study.The datasets generated during and/or analyzed during the current study are publicly available. Gene Expression Omnibus: https://www.ncbi.nlm.nih.gov/geo/
basis
The paper names GSE102083, GSE29722, GSE101685, GSE112790 in GEO database and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 1 item
[0]
survival_km
assets array · 2 items
[0]
source:pmid:35984176
[1]
data:geo:GSE101685
steps array · 1 item
[0]
run_analysis
must_build object · 5 fields
dsl_operations array · 0 items
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readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
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data:geo:GSE101685
gaps array · 0 items
review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T18:00:47Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
9271
completion_tokens
4122
cached_tokens
128
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
provider
minimax
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review.independent_reader
[1]
review.machine_critique
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review.human_critique
execution object · 5 fields
state
absent
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not_run
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null
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gaps array · 1 item
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execution.not_run
provenance object · 7 fields
entities array · 3 items
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id
pmid:35984176
type
paper
label
pmid:35984176
[1] object · 3 fields
id
source:pmid:35984176
type
manuscript
label
PMID 35984176 full text
[2] object · 3 fields
id
data:geo:GSE101685
type
dataset
label
GEO GSE101685
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
used array · 3 items
[0] object · 3 fields
id
pmid:35984176
type
paper
label
pmid:35984176
[1] object · 3 fields
id
source:pmid:35984176
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manuscript
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PMID 35984176 full text
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id
data:geo:GSE101685
type
dataset
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GEO GSE101685
agent
agent:corpus-assay-engine
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id
activity-read-35984176
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extraction
used array · 1 item
[0]
source:pmid:35984176
agent
agent:minimax-reader
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activity-resolve-GSE101685
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accession_resolution
used array · 1 item
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data:geo:GSE101685
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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agent:minimax-reader
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MiniMax literature reader
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sha256:9b06631e14e67f2dfb752ed64208228581c19fc80fb2b0602ba6f65bb77dccf4
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gaps array · 13 items
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survival_km
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supported
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dsl_catalogue
f2132e96ae6c7a4e
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35984176", "kind": "science-record", "revision": 4, "content_hash": "sha256:f27fac07f8e79c11ae32173b8a454a10a6f4aa3867eba9171f371bed6de39aff", "created_at": "2026-11-01T18:15:07Z", "updated_at": "2026-11-01T22:07:18Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of G6PC as a potential prognostic biomarker in hepatocellular carcinoma based on bioinformatics analysis.", "doi": "10.1097/MD.0000000000029548", "pmid": "35984176", "authors": ["Li Tian", "Yong Liao"], "journal": "Medicine", "year": 2022, "abstract": "Hepatocellular carcinoma (HCC) has high mortality and incidence rates around the world with limited therapeutic options. There is an urgent need for identification of novel therapeutic targets and biomarkers for early diagnosis and predicting patient survival with HCC. Several studies (GSE102083, GSE29722, GSE101685, and GSE112790) from the GEO database in HCC were screened and analyzed by GEO2R, gene ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis were conducted with the Database for Annotation, Visualization and Integrated Discovery. The protein-protein interaction network was plotted and the module analysis was performed using Search Tool for the Retrieval of Inter-acting Genes/Proteins database and Cytoscape. The expression and survival of key genes were identified using UALCAN, Kaplan-Meier Plotter and ONCOMINE online databases, and the immune infiltration level of key genes was analyzed via the Tumor Immune Estimation Resource (TIMER) database. Through database analysis, eight key genes were finally screened out, and the expressions of cyclin-dependent kinase regulatory subunit 2 and glucose-6-phosphatase catalytic (G6PC), which were closely related to the survival of HCC patients, was detected by using UALCAN. Further analysis on the differential expression of G6PC in multiple cancerous tumors and normal tissues revealed low expression in many solid tumors by Oncomine and TIMER. In addition, Kaplan-Meier plotter and UALCAN database analysis to access diseases prognosis suggested that low expression of G6PC was significantly associated with poor overall survival in HCC patients. Finally, TIMER database analysis showed a significant negative correlation between G6PC and infiltration levels of six kinds of immune cells. The somatic copy number alterations of G6PC were associated with B cells, CD8+ T cells, CD4+ T cells, macrophages, dentritic cells and neutrophils. These bioinformatic data identified G6PC as a potential key gene in the diagnosis and prognosis of HCC.", "claims": [{"id": "claim-method", "statement": "GEO2R (https://www.ncbi.nlm.nih.gov/geo/geo2r/)[21] can help us to analyze DEGs, which is an useful online software. 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Gene Expression Omnibus: https://www.ncbi.nlm.nih.gov/geo/"}], "state": "complete"}, {"id": "claim-target-result", "statement": "GEO2R analysis of four GEO microarray datasets yielded 337 common differentially expressed genes.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35984176", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Several studies (GSE102083, GSE29722, GSE101685, and GSE112790) from the GEO database in HCC were screened and analyzed by GEO2R, gene ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis were conducted with the Database for Annotation, Visualization and Integrated Discovery."}, {"asset": "source:pmid:35984176", "locator": "sections[10] \"3.1. Screening and identification of DEGs in HCC\" paragraph 2", "quote": "A sum of 337 common DEGs (Fig. 1A) was found in all four datasets, consisting of 126 upregulated genes (Fig. 1B) and 211 down-regulated genes (Fig. 1C)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "GEO2R analysis of four GEO microarray datasets yielded 337 common differentially expressed genes.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:35984176"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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