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pmid:32596394

Identification of an Individualized Prognostic Signature Based on the RWSR Model in Early-Stage Bladder Carcinoma.

Liyang Liu · Xiaodan Zhong · Haining Cui · Hao Zhang · Linyu Wang · Yuanning Liu

BioMed research international · 2020 doi:10.1155/2020/9186546

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Experiment

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Data

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title
Identification of an Individualized Prognostic Signature Based on the RWSR Model in Early-Stage Bladder Carcinoma.
doi
10.1155/2020/9186546
pmid
32596394
authors array · 6 items
[0]
Liyang Liu
[1]
Xiaodan Zhong
[2]
Haining Cui
[3]
Hao Zhang
[4]
Linyu Wang
[5]
Yuanning Liu
journal
BioMed research international
year
2020
abstract
Bladder cancer (BLCA) is the fourth common cancer among males in the United States, which is also the fourth leading cause of cancer-related death in old males. BLCA has a high recurrence rate, with over 50% of patients which has at least one recurrence within five years. Due to the complexity of the molecular mechanisms and heterogeneous cancer feature, BLCA clinicians find it hard to make an efficient management decision as they lack reliable assessment of mortality risk. Meanwhile, there is currently no screening suitable prognostic signature or method recommended for early detection, which is significantly important to early-stage detection and prognosis. In this study, a novel model, named the risk-weighted sparse regression (RWSR) model, is constructed to identify a robust signature for patients of early-stage BLCA. The 17-gene signature is generated and then validated as an independent prognostic factor in BLCA cohorts from GSE13507 and TCGA_BLCA datasets. Meanwhile, a risk score model is developed and validated among the 17-gene signature. The risk score is also considered an independent factor for prognosis prediction, which is confirmed through prognosis analysis. The Kaplan-Meier with the log-rank test is used to assess survival difference. Furthermore, the predictive capacity of the signature is proved through stratification analysis. Finally, an effective patient classification is completed by a combination of the 17-gene signature and stage information, which is for better survival prediction and treatment decisions. Besides, 11 genes in the signature, such as coiled-coil domain containing 73 (CCDC73) and protein kinase, DNA-activated, and catalytic subunit (PRKDC), are proved to be prognosis marker genes or strongly associated with prognosis and progress of other types of cancer in published literature already. As a result, this paper would more accurately predict a patient's prognosis and improve surveillance in the clinical setting, which may provide a quantitative and reliable decision-making basis for the treatment plan.
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To predict the differences between the two risk BLCA patient groups based on survival time, we use the Kaplan-Meier method and calculate the log-rank value to identify the statistical significance between groups.
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To predict the differences between the two risk BLCA patient groups based on survival time, we use the Kaplan-Meier method and calculate the log-rank value to identify the statistical significance between groups.
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The raw data of RNA-seq and clinical data from TCGA and GEO datasets are available in the Supplemental Files.
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title
Predective Value of Prognosis-Related Gene Expression Study in Primary Bladder Cancer
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General information of the 17 genes for constructing the prognostic signature.
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3.1. Prognostic Signature Generation
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General information of the 17 genes for constructing the prognostic signature.
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Univariate Cox regression analysis of 17 genes and overall survival of BLCA in two databases.
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3.1. Prognostic Signature Generation
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Univariate Cox regression analysis of 17 genes and overall survival of BLCA in two databases.
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[4]
2.3E-02
[12] array · 5 items
[0]
PRKDC
[1]
0.59 (0.4-0.86)
[2]
6.62E-03
[3]
0.41 (0.21-0.8)
[4]
9.25E-03
[13] array · 5 items
[0]
RER1
[1]
3.3 (1.2-8.9)
[2]
1.91E-02
[3]
6 (1.5-24)
[4]
1.12E-02
[14] array · 5 items
[0]
SYNPO
[1]
0.02 (0.00046-0.86)
[2]
4.15E-02
[3]
0.46 (0.26-0.81)
[4]
7.35E-03
[15] array · 5 items
[0]
XKR8
[1]
21 (1.4-300)
[2]
2.71E-02
[3]
3.7 (1.2-12)
[4]
2.55E-02
[16] array · 5 items
[0]
ZNF284
[1]
54 (1.4-2200)
[2]
3.37E-02
[3]
2.5 (1-6.1)
[4]
4.38E-02
[17] array · 5 items
[0]
ZNF680
[1]
2.3 (1.1-4.7)
[2]
2.48E-02
[3]
2.1 (1-4)
[4]
3.65E-02
[18] array · 5 items
[0]
ZNF780B
[1]
27 (1.8-390)
[2]
1.63E-02
[3]
2.7 (1.3-5.6)
[4]
9.42E-03
locator
section[9]/table-wrap[2]#tab2
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asset:table:pmid:32596394:3
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jats-table
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read_table
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Univariate and multivariate Cox regression analyses of the signature genes and overall survival.
structure object · 5 fields
pmcid
PMC7293744
section_index
11
section_title
3.3. The 17-Gene Prognostic Signature Is Independent of Other Clinicopathological Factors
row_count
23
column_count
6
table object · 8 fields
label
Table 3
caption
Univariate and multivariate Cox regression analyses of the signature genes and overall survival.
rows array · 23 items
[0] array · 4 items
[0]
Characters
[1]
Ch.description
[2]
Univariate analysis
[3]
Multivariate analysis
[1] array · 4 items
[0]
HR (95% CI for HR)
[1]
P value
[2]
HR (95% CI for HR)
[3]
P value
[2] array · 6 items
[0]
GEO
[1]
[2]
[3]
[4]
[5]
[3] array · 6 items
[0]
Sex
[1]
Female/male
[2]
1.43 (0.76-2.7)
[3]
2.58E-01
[4]
1.13 (0.82-1.55)
[5]
3.92E-02
[4] array · 6 items
[0]
Age
[1]
>70/<=70
[2]
1.15 (1.02-1.14)
[3]
9.03E-03
[4]
1.17 (1.06-1.59)
[5]
2.91E-02
[5] array · 6 items
[0]
Invasiveness
[1]
Yes/no
[2]
2.32 (1.46-3.92)
[3]
1.64E-03
[4]
1.35 (0.65-2.83)
[5]
4.23E-02
[6] array · 6 items
[0]
Intravesical therapy
[1]
Yes/no
[2]
0.67 (0.48-0.93)
[3]
1.59E-02
[4]
0.91 (0.66-1.25)
[5]
4.57E-01
[7] array · 6 items
[0]
Stage
[1]
0-III
[2]
1.79 (1.37-2.23)
[3]
2.23E-04
[4]
1.39 (1.05-1.86)
[5]
2.38E-03
[8] array · 6 items
[0]
Grade
[1]
Low/high
[2]
2.76 (1.68-4.57)
[3]
1.97E-03
[4]
1.21 (0.91-1.62)
[5]
3.93E-02
[9] array · 6 items
[0]
Event
[1]
Yes/no
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0.92 (0.51-1.6)
[3]
7.76E-01
[4]
0.46 (0.37-1.99)
[5]
1.79E-02
[10] array · 6 items
[0]
Specific survival
[1]
Alive/dead
[2]
13.02 (7.54-24)
[3]
6.62E-04
[4]
11.79 (10.94-17.38)
[5]
2.32E-03
[11] array · 6 items
[0]
Risk score
[1]
Low/high
[2]
4.45 (4.32-5.32)
[3]
3.15E-07
[4]
4.02 (4.99-8.04)
[5]
2.46E-04
[12] array · 6 items
[0]
TCGA
[1]
[2]
[3]
[4]
[5]
[13] array · 6 items
[0]
Sex
[1]
Female/male
[2]
1.12 (0.73-1.68)
[3]
7.04E-03
[4]
2.95 (0.72-12.04)
[5]
1.355E-02
[14] array · 6 items
[0]
Age
[1]
>70/<=70
[2]
1.36 (0.76-2.35)
[3]
3.77E-02
[4]
1.22 (0.53-2.79)
[5]
6.42E-02
[15] array · 6 items
[0]
Height
[1]
>170/≤170 cm
[2]
1.24 (0.99-2.5)
[3]
2.43E-03
[4]
1.09 (1.03-1.16)
[5]
4.43E-03
[16] array · 6 items
[0]
Weight
[1]
>80/≤80
[2]
0.99 (0.98-1.07)
[3]
1.49E-02
[4]
0.97 (0.93-1.05)
[5]
2.97E-02
[17] array · 6 items
[0]
Diagnosis age
[1]
Yes/no
[2]
0.62 (0.33-1.89)
[3]
4.16E-02
[4]
0.83 (0.36-1.90)
[5]
6.64E-02
[18] array · 6 items
[0]
Stage
[1]
II/III
[2]
1.62 (1.3-2.11)
[3]
2.31E-05
[4]
1.5 (0.92-2.58)
[5]
9.92E-04
[19] array · 6 items
[0]
Grade
[1]
High/low
[2]
4.75 (3.63-7.91)
[3]
9.92E-02
[4]
3.8 (2.88-8.34)
[5]
1.87E-01
[20] array · 6 items
[0]
Noninvasive history
[1]
Yes/no
[2]
0.81 (0.63-1.87)
[3]
1.04E-02
[4]
0.83 (0.43-1.57)
[5]
5.68E-02
[21] array · 6 items
[0]
Smoking
[1]
No/<15 yr/>15 yr
[2]
1.41 (1.12-1.85)
[3]
7.47E-03
[4]
1.20 (0.67-2.15)
[5]
5.53E-03
[22] array · 6 items
[0]
Risk score
[1]
High/low
[2]
3.93 (3.34-6.35)
[3]
3.57E-06
[4]
3.11 (3.09-4.24)
[5]
8.42E-04
locator
section[11]/table-wrap[1]#tab3
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asset:table:pmid:32596394:4
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The pathway enriched for the 17-gene signature based on four pathway databases.
structure object · 5 fields
pmcid
PMC7293744
section_index
14
section_title
3.6. Signature Enrichment Analysis
row_count
25
column_count
3
table object · 8 fields
label
Table 4
caption
The pathway enriched for the 17-gene signature based on four pathway databases.
rows array · 25 items
[0] array · 3 items
[0]
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[1]
Name of pathway
[2]
P value
[1] array · 3 items
[0]
1
[1]
BIOCARTA_FAS_PATHWAY
[2]
9.42E-05
[2] array · 3 items
[0]
2
[1]
BIOCARTA_G_PATHWAY
[2]
2.23E-04
[3] array · 3 items
[0]
3
[1]
BIOCARTA_G2_PATHWAY
[2]
5.99E-05
[4] array · 3 items
[0]
4
[1]
BIOCARTA_HIVNEF_PATHWAY
[2]
3.55E-04
[5] array · 3 items
[0]
5
[1]
BIOCARTA_TNFR_PATHWAY
[2]
2.04E-04
[6] array · 3 items
[0]
6
[1]
BIOCARTA_TNFR1_PATHWAY
[2]
8.8E-05
[7] array · 3 items
[0]
7
[1]
KEGG_CELL_CYCLE
[2]
1.61E-03
[8] array · 3 items
[0]
8
[1]
KEGG_LEISHMANIA_INFECTION
[2]
5.17E-04
[9] array · 3 items
[0]
9
[1]
KEGG_NATURAL_KILLER_CELL_MEDIATED_CYTOTOXICITY
[2]
1.79E-03
[10] array · 3 items
[0]
10
[1]
KEGG_NON_HOMOLOGOUS_END_JOINING
[2]
1.7E-05
[11] array · 3 items
[0]
11
[1]
KEGG_OXIDATIVE_PHOSPHORYLATION
[2]
1.77E-03
[12] array · 3 items
[0]
12
[1]
KEGG_SYSTEMIC_LUPUS_ERYTHEMATOSUS
[2]
1.9E-03
[13] array · 3 items
[0]
13
[1]
KEGG_TGF_BETA_SIGNALING_PATHWAY
[2]
7.61E-04
[14] array · 3 items
[0]
14
[1]
PID_AR_PATHWAY
[2]
3.93E-04
[15] array · 3 items
[0]
15
[1]
PID_BARD_PATHWAY
[2]
3.36E-07
[16] array · 3 items
[0]
16
[1]
PID_BARD1PATHWAY
[2]
3.36E-07
[17] array · 3 items
[0]
17
[1]
PID_DNA_PK_PATHWAY
[2]
2.61E-05
[18] array · 3 items
[0]
18
[1]
PID_DNAPK_PATHWAY
[2]
2.61E-05
[19] array · 3 items
[0]
19
[1]
PID_PI3KCIAKTPATHWAY
[2]
1.29E-04
[20] array · 3 items
[0]
20
[1]
PID_PIKCI_AKT_PATHWAY
[2]
1.29E-04
[21] array · 3 items
[0]
21
[1]
REACTOME_DNA_REPAIR
[2]
1.16E-03
[22] array · 3 items
[0]
22
[1]
REACTOME_DOUBLE_STRAND_BREAK_REPAIR
[2]
5.02E-05
[23] array · 3 items
[0]
23
[1]
REACTOME_ION_CHANNEL_TRANSPORT
[2]
3.08E-04
[24] array · 3 items
[0]
24
[1]
REACTOME_ION_TRANSPORT_BY_P_TYPE_ATPASES
[2]
1.14E-04
locator
section[14]/table-wrap[1]#tab4
gaps array · 2 items
[0]
asset:data:geo:GSE13507 not downloaded
[1]
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[0] object · 10 fields
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method-1
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survival_analysis
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log_rank_test
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Survival analysis
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logrank_test
missing_operations array · 0 items
parameters object · 0 fields
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time_to_event_with_censoring
evidence object · 3 fields
score
1
band
verbatim
quote
To predict the differences between the two risk BLCA patient groups based on survival time, we use the Kaplan-Meier method and calculate the log-rank value to identify the statistical significance between groups.
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method-2
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Survival analysis
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survival_km
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parameters object · 0 fields
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time_to_event_with_censoring
evidence object · 3 fields
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Kaplan-Meier
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method-3
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survival_analysis
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Survival analysis
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cox_ph
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time_to_event_with_censoring
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0.8
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Cox regression
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Diagnostic test evaluation
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reference_standard_and_test
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0.8
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ROC curve
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capability:computational_analysis
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gwas
candidate
Automated Assays Laravel application and simulated adapters
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nothing:replicable_now
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logrank_test
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: log_rank_test.
capability object · 4 fields
tier
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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
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GSE13507
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[0]
GSE13507
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[0]
The raw data of RNA-seq and clinical data from TCGA and GEO datasets are available in the Supplemental Files.
basis
The paper names GSE13507 in GEO and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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source:pmid:32596394
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To predict the differences between the two risk BLCA patient groups based on survival time, we use the Kaplan-Meier method and calculate the log-rank value to identify the statistical significance between groups.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:32596394", "kind": "science-record", "revision": 7, "content_hash": "sha256:f93dacbd75bf50bbd08a5ddb5e39b10e626a2acfcd4244309732bb59b0e42a2e", "created_at": "2026-11-01T15:41:04Z", "updated_at": "2026-11-01T22:01:49Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of an Individualized Prognostic Signature Based on the RWSR Model in Early-Stage Bladder Carcinoma.", "doi": "10.1155/2020/9186546", "pmid": "32596394", "authors": ["Liyang Liu", "Xiaodan Zhong", "Haining Cui", "Hao Zhang", "Linyu Wang", "Yuanning Liu"], "journal": "BioMed research international", "year": 2020, "abstract": "Bladder cancer (BLCA) is the fourth common cancer among males in the United States, which is also the fourth leading cause of cancer-related death in old males. BLCA has a high recurrence rate, with over 50% of patients which has at least one recurrence within five years. Due to the complexity of the molecular mechanisms and heterogeneous cancer feature, BLCA clinicians find it hard to make an efficient management decision as they lack reliable assessment of mortality risk. Meanwhile, there is currently no screening suitable prognostic signature or method recommended for early detection, which is significantly important to early-stage detection and prognosis. In this study, a novel model, named the risk-weighted sparse regression (RWSR) model, is constructed to identify a robust signature for patients of early-stage BLCA. The 17-gene signature is generated and then validated as an independent prognostic factor in BLCA cohorts from GSE13507 and TCGA_BLCA datasets. Meanwhile, a risk score model is developed and validated among the 17-gene signature. The risk score is also considered an independent factor for prognosis prediction, which is confirmed through prognosis analysis. The Kaplan-Meier with the log-rank test is used to assess survival difference. Furthermore, the predictive capacity of the signature is proved through stratification analysis. Finally, an effective patient classification is completed by a combination of the 17-gene signature and stage information, which is for better survival prediction and treatment decisions. Besides, 11 genes in the signature, such as coiled-coil domain containing 73 (CCDC73) and protein kinase, DNA-activated, and catalytic subunit (PRKDC), are proved to be prognosis marker genes or strongly associated with prognosis and progress of other types of cancer in published literature already. As a result, this paper would more accurately predict a patient's prognosis and improve surveillance in the clinical setting, which may provide a quantitative and reliable decision-making basis for the treatment plan.", "claims": [{"id": "claim-method", "statement": "To predict the differences between the two risk BLCA patient groups based on survival time, we use the Kaplan-Meier method and calculate the log-rank value to identify the statistical significance between groups.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32596394", "locator": "sections[7] \"2.5. 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