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pmid:31566930

Weighted gene coexpression network analysis identifies a new biomarker of CENPF for prediction disease prognosis and progression in nonmuscle invasive bladder cancer.

Jiawei Shi · Pu Zhang · Lilong Liu · Xiaobo Min · Yajun Xiao

Molecular genetics & genomic medicine · 2019 doi:10.1002/mgg3.982

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Weighted gene coexpression network analysis identifies a new biomarker of CENPF for prediction disease prognosis and progression in nonmuscle invasive bladder cancer.
doi
10.1002/mgg3.982
pmid
31566930
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Jiawei Shi
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Pu Zhang
[2]
Lilong Liu
[3]
Xiaobo Min
[4]
Yajun Xiao
journal
Molecular genetics & genomic medicine
year
2019
abstract
BACKGROUND: The dreadful prognosis of nonmuscle invasive bladder cancer mainly results from the delay in recognition of individuals with a high risk of progression. Thus, the emphasis of this work lies in developing valuable biomarkers that is conducive to accurately predicting the progression of NMIBC. METHODS: Microarray data from GSE32894 including 209 NMIBC samples were performed by weighted gene coexpression network analysis (WGCNA), which could find modules of highly correlated genes and relate modules to external sample traits. Besides, we constructed a protein-protein interaction to facilitate screening the hub gene. At last, we used RNA-seq and microarray data and clinical information from ArrayExpress (E-MTAB-4321) and GSE13507 to select and validate the candidate gene. RESULTS: In current paper, blue module of 13 gene coexpression clusters we identified was selected as the key modules. Seven genes namely: CDCA8, CENPF, MCM6, MELK, PRC1, STIL, and TPX2 have been identified as candidate genes. Notably, among them, only elevated CENPF in NIMBC tissue was closely associated with low progression-free survival (PFS) and overall survival (OS) rate in three datasets and had a large area under receiver operating characteristic (ROC) curve. Finally, CENPF was identified as an effective biomarker in NMIBC. CONCLUSION: Therefore, our findings submit a new progressive and prognostic molecular marker and therapeutic target for NMIBC. Moreover, these genes that deserve to be further researched may improve the comprehension about the occurrence and development of superficial bladder cancer.
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sample_count
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group_sizes
null
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null
platform
6947
taxon
Homo sapiens
title
A Molecular Taxonomy of Urothelial Carcinoma
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[3] object · 15 fields
id
data:geo:GSE48075
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=GSE48075
sha256
null
bytes
null
access
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resolved
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identifier
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note
For one, non‐normalized microarray gene expressing profiles and corresponding clinical data were downloaded from GSE32894 (n = 213) (Sjodahl et al., 2012) and used to screen probesets, construct of coexpression networks and identify hub genes in the present study.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
For one, non‐normalized microarray gene expressing profiles and corresponding clinical data were downloaded from GSE32894 (n = 213) (Sjodahl et al., 2012) and used to screen probesets, construct of coexpression networks and identify hub genes in the present study.
access_statement_kind
repository_route_statement
sample_accessions array · 142 items
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[39]
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[40]
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[45]
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[55]
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[64]
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[65]
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[66]
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[67]
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[68]
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[70]
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[71]
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[74]
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[100]
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[102]
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[104]
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[105]
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[110]
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[111]
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[112]
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[114]
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[118]
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[119]
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[120]
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[128]
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[129]
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[130]
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[132]
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[133]
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[134]
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[135]
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[137]
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[138]
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[139]
GSM1167472
[140]
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[141]
GSM1167474
sample_count
142
group_sizes
null
group_sizes_basis
null
platform
6947
taxon
Homo sapiens
title
Identification of subsets of urothelial carcinoma
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 · 16 fields
id
asset:table:pmid:31566930:1
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table
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jats-table
media_type
application/vnd.jats.table+json
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null
sha256
sha256:41d935caf609ed0d92847c3405737a76f7ac523f683eb58c8aa4185de4f6b364
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verified
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read_table
reader_status
available
identifier
section[16]/table-wrap[1]#mgg3982-tbl-0002
version
null
note
Univariate analysis of seven candidate genes in three cohorts
structure object · 5 fields
pmcid
PMC6825849
section_index
10
section_title
Candidate genes validation
row_count
9
column_count
10
table object · 8 fields
label
Table 2
caption
Univariate analysis of seven candidate genes in three cohorts
rows array · 9 items
[0] array · 4 items
[0]
Variables
[1]
GSE32894 Cohort
[2]
ArrayExpress Cohort (E‐MTAB‐4321)
[3]
GSE13507 Cohort
[1] array · 9 items
[0]
HR
[1]
95% CI
[2]
p‐Value
[3]
HR
[4]
95% CI
[5]
p ‐Value
[6]
HR
[7]
95% CI
[8]
p ‐Value
[2] array · 10 items
[0]
CDCA8
[1]
4.25
[2]
0.91–19.74
[3]
.065
[4]
5.7
[5]
2.19–14.86
[6]
<.001
[7]
1.66
[8]
0.87–3.18
[9]
.125
[3] array · 10 items
[0]
CENPF
[1]
4.42
[2]
1.95–20.53
[3]
.048
[4]
10.03
[5]
3.05–32.99
[6]
<.001
[7]
2.46
[8]
1.24–4.86
[9]
.01
[4] array · 10 items
[0]
MCM6
[1]
2.41
[2]
0.64–9.16
[3]
.195
[4]
5.72
[5]
2.19–14.89
[6]
<.001
[7]
1.13
[8]
0.6–2.13
[9]
.712
[5] array · 10 items
[0]
MELK
[1]
4.04
[2]
0.86–18.9
[3]
.076
[4]
4.51
[5]
1.85–11
[6]
.001
[7]
2.15
[8]
1.1–4.22
[9]
.025
[6] array · 10 items
[0]
PRC1
[1]
2.44
[2]
0.64–9.3
[3]
.19
[4]
5.53
[5]
2.12–14.41
[6]
<.001
[7]
1.97
[8]
1.02–3.81
[9]
.043
[7] array · 10 items
[0]
STIL
[1]
1.47
[2]
0.42–5.09
[3]
.544
[4]
5.58
[5]
2.14–14.54
[6]
<.001
[7]
0.92
[8]
0.49–1.75
[9]
.805
[8] array · 10 items
[0]
TPX2
[1]
5.03
[2]
1.08–23.34
[3]
.039
[4]
7.31
[5]
2.56–20.89
[6]
<.001
[7]
1.55
[8]
0.81–2.96
[9]
.188
locator
section[16]/table-wrap[1]#mgg3982-tbl-0002
[5] object · 16 fields
id
asset:table:pmid:31566930:2
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table
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jats-table
media_type
application/vnd.jats.table+json
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null
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sha256:05f339e9bca4c925e52faac638de047c14637f4e502b662ab10fecd3a0e624ac
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read_table
reader_status
available
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section[15]/table-wrap[1]#mgg3982-tbl-0001
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null
note
The detailed information of candidate genes
structure object · 5 fields
pmcid
PMC6825849
section_index
15
section_title
Functional enrichment analysis and hub genes and candidate genes identification
row_count
8
column_count
8
table object · 8 fields
label
Table 1
caption
The detailed information of candidate genes
rows array · 8 items
[0] array · 8 items
[0]
Gene symbol
[1]
Probe ID
[2]
GS T‐stage (p‐value)
[3]
GS grade (p‐value)
[4]
GS progression (p‐value)
[5]
MM (p‐value)
[6]
PPI networka
[7]
Coexpression networkb
[1] array · 8 items
[0]
CDCA8
[1]
ILMN_1709294
[2]
0.40 (2.20E‐09)
[3]
0.54 (8.80E‐17)
[4]
0.23 (8.71E‐04)
[5]
0.81 (6.66E‐50)
[6]
90
[7]
146
[2] array · 8 items
[0]
CENPF
[1]
ILMN_1664516
[2]
0.45 (1.42E‐11)
[3]
0.56 (7.46E‐19)
[4]
0.20 (3.26E‐03)
[5]
0.80 (7.43E‐48)
[6]
85
[7]
134
[3] array · 8 items
[0]
MCM6
[1]
ILMN_1798654
[2]
0.39 (4.53E‐09)
[3]
0.56 (7.74E‐19)
[4]
0.21 (2.49E‐03)
[5]
0.85 (7.89E‐60)
[6]
52
[7]
121
[4] array · 8 items
[0]
MELK
[1]
ILMN_2212909
[2]
0.44 (2.24E‐11)
[3]
0.57 (2.87E‐19)
[4]
0.22 (1.17E‐03)
[5]
0.87 (1.86E‐66)
[6]
85
[7]
201
[5] array · 8 items
[0]
PRC1
[1]
ILMN_1728934
[2]
0.40 (1.63E‐09)
[3]
0.55 (2.87E‐19)
[4]
0.22 (1.21E‐03)
[5]
0.82 (1.31E‐51)
[6]
85
[7]
193
[6] array · 8 items
[0]
STIL
[1]
ILMN_2413650
[2]
0.48 (4.29E‐13)
[3]
0.58 (2.87E‐20)
[4]
0.21 (2.73E‐03)
[5]
0.89 (1.33E‐70)
[6]
19
[7]
187
[7] array · 8 items
[0]
TPX2
[1]
ILMN_1796949
[2]
0.48 (1.73E‐13)
[3]
0.61 (1.88E‐22)
[4]
0.20 (3.32E‐03)
[5]
0.89 (1.47E‐70)
[6]
84
[7]
208
locator
section[15]/table-wrap[1]#mgg3982-tbl-0001
[6] object · 16 fields
id
asset:table:pmid:31566930:3
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table
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jats-table
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application/vnd.jats.table+json
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null
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sha256:41d935caf609ed0d92847c3405737a76f7ac523f683eb58c8aa4185de4f6b364
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open
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verified
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read_table
reader_status
available
identifier
section[16]/table-wrap[1]#mgg3982-tbl-0002
version
null
note
Univariate analysis of seven candidate genes in three cohorts
structure object · 5 fields
pmcid
PMC6825849
section_index
16
section_title
Candidate genes validation
row_count
9
column_count
10
table object · 8 fields
label
Table 2
caption
Univariate analysis of seven candidate genes in three cohorts
rows array · 9 items
[0] array · 4 items
[0]
Variables
[1]
GSE32894 Cohort
[2]
ArrayExpress Cohort (E‐MTAB‐4321)
[3]
GSE13507 Cohort
[1] array · 9 items
[0]
HR
[1]
95% CI
[2]
p‐Value
[3]
HR
[4]
95% CI
[5]
p ‐Value
[6]
HR
[7]
95% CI
[8]
p ‐Value
[2] array · 10 items
[0]
CDCA8
[1]
4.25
[2]
0.91–19.74
[3]
.065
[4]
5.7
[5]
2.19–14.86
[6]
<.001
[7]
1.66
[8]
0.87–3.18
[9]
.125
[3] array · 10 items
[0]
CENPF
[1]
4.42
[2]
1.95–20.53
[3]
.048
[4]
10.03
[5]
3.05–32.99
[6]
<.001
[7]
2.46
[8]
1.24–4.86
[9]
.01
[4] array · 10 items
[0]
MCM6
[1]
2.41
[2]
0.64–9.16
[3]
.195
[4]
5.72
[5]
2.19–14.89
[6]
<.001
[7]
1.13
[8]
0.6–2.13
[9]
.712
[5] array · 10 items
[0]
MELK
[1]
4.04
[2]
0.86–18.9
[3]
.076
[4]
4.51
[5]
1.85–11
[6]
.001
[7]
2.15
[8]
1.1–4.22
[9]
.025
[6] array · 10 items
[0]
PRC1
[1]
2.44
[2]
0.64–9.3
[3]
.19
[4]
5.53
[5]
2.12–14.41
[6]
<.001
[7]
1.97
[8]
1.02–3.81
[9]
.043
[7] array · 10 items
[0]
STIL
[1]
1.47
[2]
0.42–5.09
[3]
.544
[4]
5.58
[5]
2.14–14.54
[6]
<.001
[7]
0.92
[8]
0.49–1.75
[9]
.805
[8] array · 10 items
[0]
TPX2
[1]
5.03
[2]
1.08–23.34
[3]
.039
[4]
7.31
[5]
2.56–20.89
[6]
<.001
[7]
1.55
[8]
0.81–2.96
[9]
.188
locator
section[16]/table-wrap[1]#mgg3982-tbl-0002
gaps array · 6 items
[0]
asset:data:geo:GSE13507 not downloaded
[1]
asset:data:geo:GSE13507 licence not read
[2]
asset:data:geo:GSE32894 not downloaded
[3]
asset:data:geo:GSE32894 licence not read
[4]
asset:data:geo:GSE48075 not downloaded
[5]
asset:data:geo:GSE48075 licence not read
analysis object · 4 fields
state
partial
methods array · 2 items
[0] object · 10 fields
id
method-1
family
network_analysis
specific
ppi_network
label
Network / pathway analysis
dsl_operations array · 3 items
[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
quote
protein-protein interaction
[1] object · 10 fields
id
method-2
family
null
specific
null
label
Weighted gene coexpression network analysis (WGCNA)
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
quote
Microarray data from GSE32894 including 209 NMIBC samples were performed by weighted gene coexpression network analysis (WGCNA), which could find modules of highly correlated genes and relate modules to external sample traits.
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 · 3 items
[0]
build_graph
[1]
centrality_scores
[2]
pathway_enrich
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: ppi_network.
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 · 3 items
[0]
GSE32894
[1]
GSE48075
[2]
GSE13507
resolved_accessions array · 3 items
[0]
GSE32894
[1]
GSE48075
[2]
GSE13507
statements array · 1 item
[0]
For one, non‐normalized microarray gene expressing profiles and corresponding clinical data were downloaded from GSE32894 (n = 213) (Sjodahl et al., 2012) and used to screen probesets, construct of coexpression networks and identify hub genes in the present study.
basis
The paper names GSE32894, GSE48075, GSE13507 in GEO database and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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redicting the progression of NMIBC. METHODS: Microarray data from GSE32894 including 209 NMIBC sampl
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g the hub gene. At last, we used RNA-seq and microarray data and clinical information from ArrayExpr
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ate screening the hub gene. At last, we used RNA-seq and microarray data and clinical information
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:31566930", "kind": "science-record", "revision": 6, "content_hash": "sha256:81cb4e82aacca7cc2829f7171b1181a0529ba6694028b500781cd06295bcc53f", "created_at": "2026-11-01T15:40:50Z", "updated_at": "2026-11-01T22:00:52Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Weighted gene coexpression network analysis identifies a new biomarker of CENPF for prediction disease prognosis and progression in nonmuscle invasive bladder cancer.", "doi": "10.1002/mgg3.982", "pmid": "31566930", "authors": ["Jiawei Shi", "Pu Zhang", "Lilong Liu", "Xiaobo Min", "Yajun Xiao"], "journal": "Molecular genetics & genomic medicine", "year": 2019, "abstract": "BACKGROUND: The dreadful prognosis of nonmuscle invasive bladder cancer mainly results from the delay in recognition of individuals with a high risk of progression. Thus, the emphasis of this work lies in developing valuable biomarkers that is conducive to accurately predicting the progression of NMIBC.\nMETHODS: Microarray data from GSE32894 including 209 NMIBC samples were performed by weighted gene coexpression network analysis (WGCNA), which could find modules of highly correlated genes and relate modules to external sample traits. Besides, we constructed a protein-protein interaction to facilitate screening the hub gene. At last, we used RNA-seq and microarray data and clinical information from ArrayExpress (E-MTAB-4321) and GSE13507 to select and validate the candidate gene.\nRESULTS: In current paper, blue module of 13 gene coexpression clusters we identified was selected as the key modules. Seven genes namely: CDCA8, CENPF, MCM6, MELK, PRC1, STIL, and TPX2 have been identified as candidate genes. Notably, among them, only elevated CENPF in NIMBC tissue was closely associated with low progression-free survival (PFS) and overall survival (OS) rate in three datasets and had a large area under receiver operating characteristic (ROC) curve. Finally, CENPF was identified as an effective biomarker in NMIBC.\nCONCLUSION: Therefore, our findings submit a new progressive and prognostic molecular marker and therapeutic target for NMIBC. 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE13507"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE13507"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:31566930", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1002/mgg3.982", "sha256": 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