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pmid:34868262

Comprehensive Analysis of the Tumor Microenvironment and Ferroptosis-Related Genes Predict Prognosis with Ovarian Cancer.

Xiao-Xue Li · Li Xiong · Yu Wen · Zi-Jian Zhang

Frontiers in genetics · 2021 doi:10.3389/fgene.2021.774400

Paper

complete

Experiment

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Data

partial

Analysis

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Execution

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title
Comprehensive Analysis of the Tumor Microenvironment and Ferroptosis-Related Genes Predict Prognosis with Ovarian Cancer.
doi
10.3389/fgene.2021.774400
pmid
34868262
authors array · 4 items
[0]
Xiao-Xue Li
[1]
Li Xiong
[2]
Yu Wen
[3]
Zi-Jian Zhang
journal
Frontiers in genetics
year
2021
abstract
The early diagnosis of ovarian cancer (OC) is critical to improve the prognosis and prevent recurrence of patients. Nevertheless, there is still a lack of factors which can accurately predict it. In this study, we focused on the interaction of immune infiltration and ferroptosis and selected the ESTIMATE algorithm and 15 ferroptosis-related genes (FRGs) to construct a novel E-FRG scoring model for predicting overall survival of OC patients. The gene expression and corresponding clinical characteristics were obtained from the TCGA dataset (n = 375), GSE18520 (n = 53), and GSE32062 (n = 260). A total of 15 FRGs derived from FerrDb with the immune score and stromal score were identified in the prognostic model by using least absolute shrinkage and selection operator (LASSO)-penalized COX regression analysis. The Kaplan-Meier survival analysis and time-dependent ROC curves performed a powerful prognostic ability of the E-FRG model via multi-validation. Gene Set Enrichment Analysis and Gene Set Variation Analysis elucidate multiple potential pathways between the high and low E-FRG score group. Finally, the proteins of different genes in the model were verified in drug-resistant and non-drug-resistant tumor tissues. The results of this research provide new prospects in the role of immune infiltration and ferroptosis as a helpful tool to predict the outcome of OC patients.
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A total of 15 FRGs derived from FerrDb with the immune score and stromal score were identified in the prognostic model by using least absolute shrinkage and selection operator (LASSO)–penalized COX regression analysis.
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Diagnostic test evaluation
dsl_operations array · 6 items
[0]
confusion_counts
[1]
roc_curve
[2]
sensitivity_specificity
[3]
solve_confusion_matrix
[4]
classification_metrics
[5]
published_precision_envelope
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
reference_standard_and_test
evidence object · 3 fields
score
0.8
band
high
quote
ROC curve
targets array · 0 items
gaps array · 1 item
[0]
method.reader_differs_from_extractor
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]
cox_ph
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: cox_proportional_hazards.
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 · 2 items
[0]
GSE18520
[1]
GSE32062
resolved_accessions array · 2 items
[0]
GSE18520
[1]
GSE32062
statements array · 1 item
[0]
The data that support the findings of this study are openly available in the Cancer Genome Atlas (TCGA) database for TCGA-OV at https://www.cancer.gov/t-cga, the Gene Expression Omnibus (GEO) database for GSE32062 at https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE32062, for GSE73293 at https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE73293.
basis
The paper names GSE18520, GSE32062 in Gene Expression Omnibus (GEO) 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]
cox_ph
assets array · 2 items
[0]
source:pmid:34868262
[1]
data:geo:GSE18520
steps array · 1 item
[0]
run_analysis
must_build object · 5 fields
dsl_operations array · 0 items
converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE18520
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
2026-11-01T17:10:06Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
14071
completion_tokens
1866
cached_tokens
264
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
provider
minimax
gaps array · 3 items
[0]
review.independent_reader
[1]
review.machine_critique
[2]
review.human_critique
execution object · 5 fields
state
absent
status
not_run
mode
null
runs array · 0 items
gaps array · 1 item
[0]
execution.not_run
provenance object · 7 fields
entities array · 3 items
[0] object · 3 fields
id
pmid:34868262
type
paper
label
pmid:34868262
[1] object · 3 fields
id
source:pmid:34868262
type
manuscript
label
PMID 34868262 full text
[2] object · 3 fields
id
data:geo:GSE18520
type
dataset
label
GEO GSE18520
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:34868262
type
paper
label
pmid:34868262
[1] object · 3 fields
id
source:pmid:34868262
type
manuscript
label
PMID 34868262 full text
[2] object · 3 fields
id
data:geo:GSE18520
type
dataset
label
GEO GSE18520
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-34868262
type
extraction
used array · 1 item
[0]
source:pmid:34868262
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE18520
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE18520
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
label
Corpus assay engine
[1] object · 3 fields
id
agent:minimax-reader
type
software
label
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:34868262
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sha256:68717fd4f5dabba82b46862f5f21bfd319f04577c7dbcd06a56f8dd00c956e1d
fork_of
null
gaps array · 9 items
[0]
asset:data:geo:GSE18520 licence not read
[1]
asset:data:geo:GSE18520 not downloaded
[2]
asset:data:geo:GSE32062 licence not read
[3]
asset:data:geo:GSE32062 not downloaded
[4]
execution.not_run
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method.reader_differs_from_extractor
[6]
review.human_critique
[7]
review.independent_reader
[8]
review.machine_critique
assays array · 2 items
[0] object · 11 fields
role
data_generation
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apoptosis_assay
definition_version
99e1195c7d6f
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partial
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assay_lexicon
99e1195c7d6f
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0.99
evidence array · 2 items
[0]
en, cell viability was detected by using the CellTiter Blue® reagent (Promega, G8082, United States
[1]
to remove the reagent, and 20 μl/well of the CellTiter Blue® Reagent was added. Then, the plates we
order_basis
paper_text_order:5020
id
assay:1
[1] object · 11 fields
role
analysis
definition_id
survival_analysis
definition_version
f2132e96ae6c7a4e
required_operations array · 1 item
[0]
cox_ph
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
A total of 15 FRGs derived from FerrDb with the immune score and stromal score were identified in the prognostic model by using least absolute shrinkage and selection operator (LASSO)–penalized COX regression analysis.
order_basis
consumes_earlier_output
id
assay:2
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:34868262", "kind": "science-record", "revision": 4, "content_hash": "sha256:9b37c048f2a5fb9163635789ed0be6763b133c263feb8969dd21a611e69d7565", "created_at": "2026-11-01T17:36:34Z", "updated_at": "2026-11-01T22:05:17Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Comprehensive Analysis of the Tumor Microenvironment and Ferroptosis-Related Genes Predict Prognosis with Ovarian Cancer.", "doi": "10.3389/fgene.2021.774400", "pmid": "34868262", "authors": ["Xiao-Xue Li", "Li Xiong", "Yu Wen", "Zi-Jian Zhang"], "journal": "Frontiers in genetics", "year": 2021, "abstract": "The early diagnosis of ovarian cancer (OC) is critical to improve the prognosis and prevent recurrence of patients. Nevertheless, there is still a lack of factors which can accurately predict it. In this study, we focused on the interaction of immune infiltration and ferroptosis and selected the ESTIMATE algorithm and 15 ferroptosis-related genes (FRGs) to construct a novel E-FRG scoring model for predicting overall survival of OC patients. The gene expression and corresponding clinical characteristics were obtained from the TCGA dataset (n = 375), GSE18520 (n = 53), and GSE32062 (n = 260). A total of 15 FRGs derived from FerrDb with the immune score and stromal score were identified in the prognostic model by using least absolute shrinkage and selection operator (LASSO)-penalized COX regression analysis. The Kaplan-Meier survival analysis and time-dependent ROC curves performed a powerful prognostic ability of the E-FRG model via multi-validation. Gene Set Enrichment Analysis and Gene Set Variation Analysis elucidate multiple potential pathways between the high and low E-FRG score group. Finally, the proteins of different genes in the model were verified in drug-resistant and non-drug-resistant tumor tissues. 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