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pmid:30755640

Prognostic nomogram of hypoxia-related genes predicting overall survival of colorectal cancer-Analysis of TCGA database.

Joon-Hyop Lee · Sohee Jung · Won Seo Park · Eun Kyung Choe · Eunyoung Kim · Rumi Shin · Seung Chul Heo · Jae Hyun Lee · Kwangsoo Kim · Young Jun Chai

Scientific reports · 2019 doi:10.1038/s41598-018-38116-y

Paper

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Experiment

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Data

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title
Prognostic nomogram of hypoxia-related genes predicting overall survival of colorectal cancer-Analysis of TCGA database.
doi
10.1038/s41598-018-38116-y
pmid
30755640
authors array · 10 items
[0]
Joon-Hyop Lee
[1]
Sohee Jung
[2]
Won Seo Park
[3]
Eun Kyung Choe
[4]
Eunyoung Kim
[5]
Rumi Shin
[6]
Seung Chul Heo
[7]
Jae Hyun Lee
[8]
Kwangsoo Kim
[9]
Young Jun Chai
journal
Scientific reports
year
2019
abstract
Hypoxia-related gene (HRG) expression is associated with survival outcomes of colorectal cancer (CRC). Our aim was developing a nomogram predicting CRC overall survival (OS) with HRGs and clinicopathological factors. The Cancer Genome Atlas (TCGA) database was used as discovery cohort and two Gene Expression Omnibus databases (GSE39582 and GSE41258) served as validation cohorts. A genetic risk score model prognosticating OS was developed using mRNA expression level of HRGs. Nomogram predicting OS was developed using genetic risk score model and clinicopathological variables. The genetic risk score model included four HRGs (HSPA1L, PUM1, UBE2D2, and HSP27) and successfully prognosticated OS of discovery and two validation cohorts (p < 0.001 for TCGA discovery set, p < 0.003 for the GSE39582 and p = 0.042 for the GSE41258 datasets). Nomogram included genetic risk score, age, and TNM stage. Harrell's concordance indexes of the nomogram were higher than those of TNM stage alone in the discovery set (0.77 vs. 0.69, p < 0.001), GSE39582 (0.65 vs. 0.63, p < 0.001), and GSE41258 datasets (0.78 vs. 0.77, p < 0.001). Our nomogram successfully predicted OS of CRC patients. The mRNA expression level of the HRGs might be useful as an ancillary marker for prognosticating CRC outcome.
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To evaluate the prognostic value of the genetic risk score in the context of other clinical variables, univariate and multivariate Cox analyses for OS were performed, including the genetic risk score and the conventional clinicopathologic variables (age, gender, TNM stage, KRAS mutation, BRAF mutation, and microsatellite instability).
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sections[12] "Incorporating clinical factors to predict cancer survival" paragraph 2
quote
To evaluate the prognostic value of the genetic risk score in the context of other clinical variables, univariate and multivariate Cox analyses for OS were performed, including the genetic risk score and the conventional clinicopathologic variables (age, gender, TNM stage, KRAS mutation, BRAF mutation, and microsatellite instability).
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The data that support the findings of this study are available from the Cancer Genome Atlas (TCGA, http://cancergenome.nih.gov/) COADREAD project and Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/), accession number GSE39582 and GSE41258.
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sections[16] "Data Availability" paragraph 2
quote
The data that support the findings of this study are available from the Cancer Genome Atlas (TCGA, http://cancergenome.nih.gov/) COADREAD project and Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/), accession number GSE39582 and GSE41258.
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https://doi.org/10.1038/s41598-018-38116-y
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The data that support the findings of this study are available from the Cancer Genome Atlas (TCGA, http://cancergenome.nih.gov/) COADREAD project and Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/), accession number GSE39582 and GSE41258.
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sample_count
585
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Gene expression Classification of Colon Cancer defines six molecular subtypes with distinct clinical, molecular and survival characteristics [Expression]
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
id
data:geo:GSE41258
role
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null
note
The data that support the findings of this study are available from the Cancer Genome Atlas (TCGA, http://cancergenome.nih.gov/) COADREAD project and Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/), accession number GSE39582 and GSE41258.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The data that support the findings of this study are available from the Cancer Genome Atlas (TCGA, http://cancergenome.nih.gov/) COADREAD project and Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/), accession number GSE39582 and GSE41258.
access_statement_kind
data_availability_statement
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sample_count
390
group_sizes
null
group_sizes_basis
null
platform
96
taxon
Homo sapiens
title
Expression data from colorectal cancer patients
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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[3] object · 16 fields
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asset:table:pmid:30755640:1
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Patient characteristics of datasets.
structure object · 5 fields
pmcid
PMC6372658
section_index
3
section_title
Baseline characteristics
row_count
17
column_count
6
table object · 8 fields
label
Table 1
caption
Patient characteristics of datasets.
rows array · 17 items
[0] array · 3 items
[0]
Discovery cohort
[1]
Validation cohort
[2]
Validation cohort
[1] array · 3 items
[0]
TCGA (n = 355)
[1]
GSE39582 (n = 557)
[2]
GSE41258 (n = 185
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[0]
Characteristic
[1]
n (%)
[2]
Characteristic
[3]
n (%)
[4]
Characteristic
[5]
n (%)
[3] array · 3 items
[0]
Age at diagnosis
[1]
Age at diagnosis
[2]
Age at diagnosis
[4] array · 6 items
[0]
Mean (SD)
[1]
64.5 (13.3)
[2]
Mean (SD)
[3]
66.8 (13.3)
[4]
Mean (SD)
[5]
63.5 (14.0)
[5] array · 3 items
[0]
AJCC TNM stage
[1]
AJCC TNM stage
[2]
AJCC TNM stage
[6] array · 6 items
[0]
I
[1]
56 (15.8)
[2]
I
[3]
31 (5.6)
[4]
I
[5]
28 (15.1)
[7] array · 6 items
[0]
II
[1]
135 (38.0)
[2]
II
[3]
262 (47.0)
[4]
II
[5]
50 (27.0)
[8] array · 6 items
[0]
III
[1]
112 (31.5)
[2]
III
[3]
204 (36.6)
[4]
III
[5]
49 (26.5)
[9] array · 6 items
[0]
IV
[1]
52 (14.7)
[2]
IV
[3]
60 (10.8)
[4]
IV
[5]
58 (31.4)
[10] array · 6 items
[0]
Survival event
[1]
[2]
Survival event
[3]
[4]
Survival event
[5]
[11] array · 6 items
[0]
Dead
[1]
78 (22.0)
[2]
Dead
[3]
190 (34.1)
[4]
Dead
[5]
102 (55.1)
[12] array · 6 items
[0]
Alive
[1]
277 (78.0)
[2]
Alive
[3]
367 (65.9)
[4]
Alive
[5]
83 (44.9)
[13] array · 3 items
[0]
Median follow-up time, months (range)
[1]
Median follow-up time, months (range)
[2]
Median follow-up time, months (range)
[14] array · 6 items
[0]
[1]
22 (0–148)
[2]
[3]
52 (0–201)
[4]
[5]
66 (0–203)
[15] array · 3 items
[0]
Median time to survival event, months (range)
[1]
Median time to survival event, months (range)
[2]
Median time to survival event, months (range)
[16] array · 6 items
[0]
[1]
17 (1–100)
[2]
[3]
31 (0–183)
[4]
[5]
34 (0–196)
locator
section[3]/table-wrap[1]#Tab1
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asset:table:pmid:30755640:2
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read_table
reader_status
available
identifier
section[6]/table-wrap[1]#Tab2
version
null
note
Univariate and multivariate Cox-regression results of factors related to overall survival.
structure object · 5 fields
pmcid
PMC6372658
section_index
6
section_title
Incorporating clinical factors to predict cancer survival
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13
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8
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label
Table 2
caption
Univariate and multivariate Cox-regression results of factors related to overall survival.
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Univariate analysis
[1]
Multivariate analysis
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[0]
Variables
[1]
Hazard Ratio (95% CI)
[2]
P value
[3]
Variables
[4]
Hazard Ratio (95% CI)
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P value
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Genetic risk score (High risk vs. low risk)
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4.221
[2]
(2.536–7.026)
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<0.001
[4]
Genetic risk score (High risk vs. low risk)
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3.402
[6]
(2.873–3.93)
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<0.001
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Age
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1.025
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0.006
[4]
Age
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1.029
[6]
(1.009–1.049)
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0.004
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Male gender
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1.264
[2]
(0.805–1.985)
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0.307
[4]
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1.062
[6]
(0.598–1.527)
[7]
0.798
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[0]
AJCC TNM stage
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[2]
[3]
<0.001
[4]
AJCC TNM stage
[5]
[6]
[7]
<0.001
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I
[1]
1.000 (reference)
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[3]
I
[4]
1.000 (reference)
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[0]
II
[1]
1.450
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[4]
II
[5]
1.057
[6]
(0.066–2.048)
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[8] array · 8 items
[0]
III
[1]
2.820
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(1.090–7.293)
[3]
[4]
III
[5]
2.082
[6]
(1.115–3.049)
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[0]
IV
[1]
6.511
[2]
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[4]
IV
[5]
5.733
[6]
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[0]
KRAS mutation
[1]
0.797
[2]
(0.505–1.257)
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0.325
[4]
KRAS mutation
[5]
0.805
[6]
(0.31–1.3)
[7]
0.389
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[0]
BRAF mutation
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1.257
[2]
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[3]
0.464
[4]
BRAF mutation
[5]
1.327
[6]
(0.504–2.151)
[7]
0.508
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[0]
MSI-high
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0.800
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0.481
[4]
MSI-high
[5]
0.759
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(−0.106–1.6)
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0.526
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section[6]/table-wrap[1]#Tab2
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note
Univariate and multivariate Cox-regression results of factors related to overall survival.
structure object · 5 fields
pmcid
PMC6372658
section_index
12
section_title
Incorporating clinical factors to predict cancer survival
row_count
13
column_count
8
table object · 8 fields
label
Table 2
caption
Univariate and multivariate Cox-regression results of factors related to overall survival.
rows array · 13 items
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[0]
Univariate analysis
[1]
Multivariate analysis
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[0]
Variables
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Hazard Ratio (95% CI)
[2]
P value
[3]
Variables
[4]
Hazard Ratio (95% CI)
[5]
P value
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[0]
Genetic risk score (High risk vs. low risk)
[1]
4.221
[2]
(2.536–7.026)
[3]
<0.001
[4]
Genetic risk score (High risk vs. low risk)
[5]
3.402
[6]
(2.873–3.93)
[7]
<0.001
[3] array · 8 items
[0]
Age
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1.025
[2]
(1.007–1.044)
[3]
0.006
[4]
Age
[5]
1.029
[6]
(1.009–1.049)
[7]
0.004
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[0]
Male gender
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1.264
[2]
(0.805–1.985)
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0.307
[4]
Male gender
[5]
1.062
[6]
(0.598–1.527)
[7]
0.798
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[0]
AJCC TNM stage
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[3]
<0.001
[4]
AJCC TNM stage
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[6]
[7]
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1.000 (reference)
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[3]
I
[4]
1.000 (reference)
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II
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1.450
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[4]
II
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1.057
[6]
(0.066–2.048)
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III
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2.820
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[3]
[4]
III
[5]
2.082
[6]
(1.115–3.049)
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IV
[1]
6.511
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[3]
[4]
IV
[5]
5.733
[6]
(4.739–6.726)
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[10] array · 8 items
[0]
KRAS mutation
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0.797
[2]
(0.505–1.257)
[3]
0.325
[4]
KRAS mutation
[5]
0.805
[6]
(0.31–1.3)
[7]
0.389
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[0]
BRAF mutation
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1.257
[2]
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[3]
0.464
[4]
BRAF mutation
[5]
1.327
[6]
(0.504–2.151)
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0.508
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MSI-high
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0.800
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0.481
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MSI-high
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0.759
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(−0.106–1.6)
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0.526
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section[6]/table-wrap[1]#Tab2
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time_to_event_with_censoring
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quote
To evaluate the prognostic value of the genetic risk score in the context of other clinical variables, univariate and multivariate Cox analyses for OS were performed, including the genetic risk score and the conventional clinicopathologic variables (age, gender, TNM stage, KRAS mutation, BRAF mutation, and microsatellite instability).
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capability object · 3 fields
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candidate
Automated Assays Laravel application and simulated adapters
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cox_ph
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards.
capability object · 4 fields
tier
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capability_id
capability:computational_analysis
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owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
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[0]
GSE39582
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GSE41258
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GSE39582
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GSE41258
statements array · 1 item
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The data that support the findings of this study are available from the Cancer Genome Atlas (TCGA, http://cancergenome.nih.gov/) COADREAD project and Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/), accession number GSE39582 and GSE41258.
basis
The paper names GSE39582, GSE41258 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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To evaluate the prognostic value of the genetic risk score in the context of other clinical variables, univariate and multivariate Cox analyses for OS were performed, including the genetic risk score and the conventional clinicopathologic variables (age, gender, TNM stage, KRAS mutation, BRAF mutation, and microsatellite instability).
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:30755640", "kind": "science-record", "revision": 4, "content_hash": "sha256:f96fe222e6d434c45f84451322d723d096bb2e5c8680c35a7a35a36333893a49", "created_at": "2026-11-01T15:40:42Z", "updated_at": "2026-11-01T21:21:59Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Prognostic nomogram of hypoxia-related genes predicting overall survival of colorectal cancer-Analysis of TCGA database.", "doi": "10.1038/s41598-018-38116-y", "pmid": "30755640", "authors": ["Joon-Hyop Lee", "Sohee Jung", "Won Seo Park", "Eun Kyung Choe", "Eunyoung Kim", "Rumi Shin", "Seung Chul Heo", "Jae Hyun Lee", "Kwangsoo Kim", "Young Jun Chai"], "journal": "Scientific reports", "year": 2019, "abstract": "Hypoxia-related gene (HRG) expression is associated with survival outcomes of colorectal cancer (CRC). Our aim was developing a nomogram predicting CRC overall survival (OS) with HRGs and clinicopathological factors. The Cancer Genome Atlas (TCGA) database was used as discovery cohort and two Gene Expression Omnibus databases (GSE39582 and GSE41258) served as validation cohorts. A genetic risk score model prognosticating OS was developed using mRNA expression level of HRGs. Nomogram predicting OS was developed using genetic risk score model and clinicopathological variables. The genetic risk score model included four HRGs (HSPA1L, PUM1, UBE2D2, and HSP27) and successfully prognosticated OS of discovery and two validation cohorts (p < 0.001 for TCGA discovery set, p < 0.003 for the GSE39582 and p = 0.042 for the GSE41258 datasets). Nomogram included genetic risk score, age, and TNM stage. Harrell's concordance indexes of the nomogram were higher than those of TNM stage alone in the discovery set (0.77 vs. 0.69, p < 0.001), GSE39582 (0.65 vs. 0.63, p < 0.001), and GSE41258 datasets (0.78 vs. 0.77, p < 0.001). Our nomogram successfully predicted OS of CRC patients. 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