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pmid:35875673

Identification of Candidate Genes Associated With Prognosis in Glioblastoma.

Rongjie Li · Qiulan Jiang · Chunhai Tang · Liechun Chen · Deyan Kong · Chun Zou · Yan Lin · Jiefeng Luo · Donghua Zou

Frontiers in molecular neuroscience · 2022 doi:10.3389/fnmol.2022.913328

Paper

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Data

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title
Identification of Candidate Genes Associated With Prognosis in Glioblastoma.
doi
10.3389/fnmol.2022.913328
pmid
35875673
authors array · 9 items
[0]
Rongjie Li
[1]
Qiulan Jiang
[2]
Chunhai Tang
[3]
Liechun Chen
[4]
Deyan Kong
[5]
Chun Zou
[6]
Yan Lin
[7]
Jiefeng Luo
[8]
Donghua Zou
journal
Frontiers in molecular neuroscience
year
2022
abstract
Background: Glioblastoma (GBM) is the most common malignant primary brain tumor, which associated with extremely poor prognosis. Methods: Data from datasets GSE16011, GSE7696, GSE50161, GSE90598 and The Cancer Genome Atlas (TCGA) were analyzed to identify differentially expressed genes (DEGs) between patients and controls. DEGs common to all five datasets were analyzed for functional enrichment and for association with overall survival using Cox regression. Candidate genes were further screened using least absolute shrinkage and selection operator (LASSO) and random forest algorithms, and the effects of candidate genes on prognosis were explored using a Gaussian mixed model, a risk model, and concordance cluster analysis. We also characterized the GBM landscape of immune cell infiltration, methylation, and somatic mutations. Results: We identified 3,139 common DEGs, which were associated mainly with PI3K-Akt signaling, focal adhesion, and Hippo signaling. Cox regression identified 106 common DEGs that were significantly associated with overall survival. LASSO and random forest algorithms identified six candidate genes (AEBP1, ANXA2R, MAP1LC3A, TMEM60, PRRG3 and RPS4X) that predicted overall survival and GBM recurrence. AEBP1 showed the best prognostic performance. We found that GBM tissues were heavily infiltrated by T helper cells and macrophages, which correlated with higher AEBP1 expression. Stratifying patients based on the six candidate genes led to two groups with significantly different overall survival. Somatic mutations in AEBP1 and modified methylation of MAP1LC3A were associated with GBM. Conclusion: We have identified candidate genes, particularly AEBP1, strongly associated with GBM prognosis, which may help in efforts to understand and treat the disease.
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Candidate genes were further screened using least absolute shrinkage and selection operator (LASSO) and random forest algorithms, and the effects of candidate genes on prognosis were explored using a Gaussian mixed model, a risk model, and concordance cluster analysis.
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Candidate genes were further screened using least absolute shrinkage and selection operator (LASSO) and random forest algorithms, and the effects of candidate genes on prognosis were explored using a Gaussian mixed model, a risk model, and concordance cluster analysis.
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The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.
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LASSO and random forest algorithms identified six candidate genes, with AEBP1 showing the best prognostic performance.
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sections[0] "Abstract" paragraph 3
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LASSO and random forest algorithms identified six candidate genes (AEBP1, ANXA2R, MAP1LC3A, TMEM60, PRRG3 and RPS4X) that predicted overall survival and GBM recurrence. AEBP1 showed the best prognostic performance.
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LASSO and random forest algorithms identified six candidate genes, with AEBP1 showing the best prognostic performance.
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access_statement_verbatim
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.
access_statement_kind
data_availability_statement
sample_accessions array · 130 items
[0]
GSM1214834
[1]
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[2]
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[6]
GSM1214840
[7]
GSM1214841
[8]
GSM1214842
[9]
GSM1214843
[10]
GSM1214844
[11]
GSM1214845
[12]
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[13]
GSM1214847
[14]
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[16]
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[17]
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[18]
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[19]
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[20]
GSM1214854
[21]
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[22]
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[23]
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[24]
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[25]
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[26]
GSM1214860
[27]
GSM1214861
[28]
GSM1214862
[29]
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[30]
GSM1214864
[31]
GSM1214865
[32]
GSM1214866
[33]
GSM1214867
[34]
GSM1214868
[35]
GSM1214869
[36]
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[37]
GSM1214871
[38]
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[39]
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[40]
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[41]
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[42]
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[43]
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[44]
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[45]
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[46]
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[47]
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[48]
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[49]
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[50]
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[51]
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[52]
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[53]
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[54]
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[55]
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[56]
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[57]
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[58]
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[59]
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[60]
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[61]
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[62]
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[63]
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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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[69]
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[70]
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[71]
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[72]
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[73]
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[74]
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[75]
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[76]
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[77]
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[78]
GSM1214912
[79]
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[80]
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[81]
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[82]
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[83]
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[84]
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[85]
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[86]
GSM1214920
[87]
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[88]
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[89]
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[90]
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[91]
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[92]
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[93]
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[94]
GSM1214928
[95]
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[96]
GSM1214930
[97]
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[98]
GSM1214932
[99]
GSM1214933
[100]
GSM1214934
[101]
GSM1214935
[102]
GSM1214936
[103]
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[104]
GSM1214938
[105]
GSM1214939
[106]
GSM1214940
[107]
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[108]
GSM1214942
[109]
GSM1214943
[110]
GSM1214944
[111]
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[112]
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[113]
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[114]
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[115]
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[116]
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[117]
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[118]
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[119]
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[120]
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[121]
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[122]
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[123]
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[124]
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[125]
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[126]
GSM1214960
[127]
GSM1214961
[128]
GSM1214962
[129]
GSM1214963
sample_count
130
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Expression data from human brain tumors and human normal brain
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:GSE7696
role
raw
format
geo-series
media_type
application/vnd.ncbi.geo-series+json
uri
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE7696
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE7696
version
null
note
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.
access_statement_kind
data_availability_statement
sample_accessions array · 84 items
[0]
GSM187153
[1]
GSM187154
[2]
GSM187155
[3]
GSM187156
[4]
GSM187157
[5]
GSM187158
[6]
GSM187159
[7]
GSM187160
[8]
GSM187161
[9]
GSM187162
[10]
GSM187163
[11]
GSM187164
[12]
GSM187165
[13]
GSM187166
[14]
GSM187167
[15]
GSM187168
[16]
GSM187169
[17]
GSM187170
[18]
GSM187171
[19]
GSM187172
[20]
GSM187173
[21]
GSM187174
[22]
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[23]
GSM187176
[24]
GSM187177
[25]
GSM187178
[26]
GSM187179
[27]
GSM187180
[28]
GSM187181
[29]
GSM187182
[30]
GSM187183
[31]
GSM187184
[32]
GSM187185
[33]
GSM187186
[34]
GSM187187
[35]
GSM187188
[36]
GSM187189
[37]
GSM187190
[38]
GSM187191
[39]
GSM187192
[40]
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[41]
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[42]
GSM187195
[43]
GSM187196
[44]
GSM187197
[45]
GSM187198
[46]
GSM187199
[47]
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[48]
GSM187201
[49]
GSM187202
[50]
GSM187203
[51]
GSM187204
[52]
GSM187205
[53]
GSM187206
[54]
GSM187207
[55]
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[56]
GSM187209
[57]
GSM187210
[58]
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[59]
GSM187212
[60]
GSM187213
[61]
GSM187214
[62]
GSM187215
[63]
GSM187216
[64]
GSM187217
[65]
GSM187218
[66]
GSM187219
[67]
GSM187220
[68]
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[69]
GSM187222
[70]
GSM187223
[71]
GSM187224
[72]
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[73]
GSM187226
[74]
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[75]
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[76]
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[77]
GSM187230
[78]
GSM187231
[79]
GSM187232
[80]
GSM187233
[81]
GSM187234
[82]
GSM187235
[83]
GSM187236
sample_count
84
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Glioblastoma from a homogenous cohort of patients treated within clinical trial
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[5] object · 15 fields
id
data:geo:GSE90598
role
raw
format
geo-series
media_type
application/vnd.ncbi.geo-series+json
uri
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE90598
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE90598
version
null
note
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.
access_statement_kind
data_availability_statement
sample_accessions array · 25 items
[0]
GSM2407485
[1]
GSM2407486
[2]
GSM2407487
[3]
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[4]
GSM2407489
[5]
GSM2407490
[6]
GSM2407491
[7]
GSM2407492
[8]
GSM2407493
[9]
GSM2407494
[10]
GSM2407495
[11]
GSM2407496
[12]
GSM2407497
[13]
GSM2407498
[14]
GSM2407499
[15]
GSM2407500
[16]
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[17]
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[18]
GSM2407503
[19]
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[20]
GSM2407505
[21]
GSM2407506
[22]
GSM2407507
[23]
GSM2407508
[24]
GSM2407509
sample_count
25
group_sizes
null
group_sizes_basis
null
platform
17692
taxon
Homo sapiens
title
Gene Expression data from Glioblastoma Multiforme patient tumor samples, healthy brain tissue (partly from GBM patients) and NHA cell line and Human fetal astrocyte cell line
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 10 items
[0]
asset:data:geo:GSE16011 not downloaded
[1]
asset:data:geo:GSE16011 licence not read
[2]
asset:data:geo:GSE36278 not downloaded
[3]
asset:data:geo:GSE36278 licence not read
[4]
asset:data:geo:GSE50161 not downloaded
[5]
asset:data:geo:GSE50161 licence not read
[6]
asset:data:geo:GSE7696 not downloaded
[7]
asset:data:geo:GSE7696 licence not read
[8]
asset:data:geo:GSE90598 not downloaded
[9]
asset:data:geo:GSE90598 licence not read
analysis object · 4 fields
state
partial
methods array · 3 items
[0] object · 10 fields
id
method-1
family
machine_learning
specific
random_forest
label
Machine learning
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
machine_learning_random_forest
expressible
false
parameters object · 0 fields
data_shapes array · 1 item
[0]
labelled_feature_matrix
evidence object · 3 fields
score
1
band
verbatim
quote
Candidate genes were further screened using least absolute shrinkage and selection operator (LASSO) and random forest algorithms, and the effects of candidate genes on prognosis were explored using a Gaussian mixed model, a risk model, and concordance cluster analysis.
[1] object · 10 fields
id
method-2
family
survival_analysis
specific
cox_proportional_hazards
label
Survival analysis
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[0]
cox_ph
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
band
medium
quote
Cox regression
[2] object · 10 fields
id
method-3
family
regression_modelling
specific
mixed_effects
label
Regression modelling
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
regression_modelling_mixed_effects
expressible
false
parameters object · 0 fields
data_shapes array · 1 item
[0]
predictors_and_outcome
evidence object · 3 fields
score
0.7
band
medium
quote
mixed model
targets array · 0 items
gaps array · 2 items
[0]
method.reader_differs_from_extractor
[1]
method.machine_learning_random_forest
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
false
required_operations array · 0 items
missing_operations array · 1 item
[0]
machine_learning_random_forest
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: random_forest.
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 · 5 items
[0]
GSE16011
[1]
GSE7696
[2]
GSE50161
[3]
GSE90598
[4]
GSE36278
resolved_accessions array · 5 items
[0]
GSE16011
[1]
GSE7696
[2]
GSE50161
[3]
GSE90598
[4]
GSE36278
statements array · 1 item
[0]
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.
basis
The paper names GSE16011, GSE7696, GSE50161, GSE90598, GSE36278 in Gene Expression Omnibus and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 0 items
assets array · 2 items
[0]
source:pmid:35875673
[1]
data:geo:GSE16011
steps array · 0 items
must_build object · 5 fields
dsl_operations array · 1 item
[0] object · 3 fields
operation
machine_learning_random_forest
priority
null
converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE16011
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
2026-11-01T17:56:49Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
12139
completion_tokens
2436
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
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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
[0] object · 3 fields
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pmid:35875673
type
paper
label
pmid:35875673
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id
source:pmid:35875673
type
manuscript
label
PMID 35875673 full text
[2] object · 3 fields
id
data:geo:GSE16011
type
dataset
label
GEO GSE16011
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[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
used array · 3 items
[0] object · 3 fields
id
pmid:35875673
type
paper
label
pmid:35875673
[1] object · 3 fields
id
source:pmid:35875673
type
manuscript
label
PMID 35875673 full text
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id
data:geo:GSE16011
type
dataset
label
GEO GSE16011
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-35875673
type
extraction
used array · 1 item
[0]
source:pmid:35875673
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE16011
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE16011
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
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[1] object · 3 fields
id
agent:minimax-reader
type
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MiniMax literature reader
source_run_id
reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
2cb3e42f047d2ecf
snapshot_id
ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:35875673
parent_hash
sha256:d730b2acf9195d86c3b4f4d5194996b428376572713e77f9838fa0f41f1e564c
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null
gaps array · 17 items
[0]
asset:data:geo:GSE16011 licence not read
[1]
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[2]
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[3]
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[4]
asset:data:geo:GSE50161 licence not read
[5]
asset:data:geo:GSE50161 not downloaded
[6]
asset:data:geo:GSE7696 licence not read
[7]
asset:data:geo:GSE7696 not downloaded
[8]
asset:data:geo:GSE90598 licence not read
[9]
asset:data:geo:GSE90598 not downloaded
[10]
execution.not_run
[11]
method.machine_learning_random_forest
[12]
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[13]
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[14]
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[15]
review.machine_critique
[16]
step:run_analysis blocked on method:machine_learning_random_forest
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
machine_learning
definition_version
f2132e96ae6c7a4e
required_operations array · 0 items
support_state
partial
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dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
Candidate genes were further screened using least absolute shrinkage and selection operator (LASSO) and random forest algorithms, and the effects of candidate genes on prognosis were explored using a Gaussian mixed model, a risk model, and concordance cluster analysis.
order_basis
analysis_only
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assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35875673", "kind": "science-record", "revision": 4, "content_hash": "sha256:c4bdaafc69e072a0a4091cd9d18db16687e4273390f3379afb1a6e2214f454f5", "created_at": "2026-11-01T18:14:58Z", "updated_at": "2026-11-01T22:07:07Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of Candidate Genes Associated With Prognosis in Glioblastoma.", "doi": "10.3389/fnmol.2022.913328", "pmid": "35875673", "authors": ["Rongjie Li", "Qiulan Jiang", "Chunhai Tang", "Liechun Chen", "Deyan Kong", "Chun Zou", "Yan Lin", "Jiefeng Luo", "Donghua Zou"], "journal": "Frontiers in molecular neuroscience", "year": 2022, "abstract": "Background: Glioblastoma (GBM) is the most common malignant primary brain tumor, which associated with extremely poor prognosis.\nMethods: Data from datasets GSE16011, GSE7696, GSE50161, GSE90598 and The Cancer Genome Atlas (TCGA) were analyzed to identify differentially expressed genes (DEGs) between patients and controls. DEGs common to all five datasets were analyzed for functional enrichment and for association with overall survival using Cox regression. Candidate genes were further screened using least absolute shrinkage and selection operator (LASSO) and random forest algorithms, and the effects of candidate genes on prognosis were explored using a Gaussian mixed model, a risk model, and concordance cluster analysis. We also characterized the GBM landscape of immune cell infiltration, methylation, and somatic mutations.\nResults: We identified 3,139 common DEGs, which were associated mainly with PI3K-Akt signaling, focal adhesion, and Hippo signaling. Cox regression identified 106 common DEGs that were significantly associated with overall survival. LASSO and random forest algorithms identified six candidate genes (AEBP1, ANXA2R, MAP1LC3A, TMEM60, PRRG3 and RPS4X) that predicted overall survival and GBM recurrence. AEBP1 showed the best prognostic performance. We found that GBM tissues were heavily infiltrated by T helper cells and macrophages, which correlated with higher AEBP1 expression. Stratifying patients based on the six candidate genes led to two groups with significantly different overall survival. Somatic mutations in AEBP1 and modified methylation of MAP1LC3A were associated with GBM.\nConclusion: We have identified candidate genes, particularly AEBP1, strongly associated with GBM prognosis, which may help in efforts to understand and treat the disease.", "claims": [{"id": "claim-method", "statement": "Candidate genes were further screened using least absolute shrinkage and selection operator (LASSO) and random forest algorithms, and the effects of candidate genes on prognosis were explored using a Gaussian mixed model, a risk model, and concordance cluster analysis.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35875673", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Candidate genes were further screened using least absolute shrinkage and selection operator (LASSO) and random forest algorithms, and the effects of candidate genes on prognosis were explored using a Gaussian mixed model, a risk model, and concordance cluster analysis."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35875673", "locator": "sections[23] \"Data Availability Statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s."}], "state": "complete"}, {"id": "claim-target-result", "statement": "LASSO and random forest algorithms identified six candidate genes, with AEBP1 showing the best prognostic performance.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35875673", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "LASSO and random forest algorithms identified six candidate genes (AEBP1, ANXA2R, MAP1LC3A, TMEM60, PRRG3 and RPS4X) that predicted overall survival and GBM recurrence. 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