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pmid:36407421

Expression pattern and diagnostic value of ferroptosis-related genes in acute myocardial infarction.

Jiahe Wu · Huanhuan Cai · Zhe Lei · Chenze Li · Yushuang Hu · Tong Zhang · Haoyan Zhu · Yi Lu · Jianlei Cao · Xiaorong Hu

Frontiers in cardiovascular medicine · 2022 doi:10.3389/fcvm.2022.993592

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
id
pmid:36407421
kind
science-record
content_hash
sha256:56365272382b4c895bafca1b0a889e030b62d1335c8f16a9ca624108c26f5c2c
schema
https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T19:00:52Z
updated_at
2026-11-01T22:08:08Z
generator object · 2 fields
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corpus-assay-engine
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reading-sci-2026-11-01
paper object · 10 fields
state
complete
title
Expression pattern and diagnostic value of ferroptosis-related genes in acute myocardial infarction.
doi
10.3389/fcvm.2022.993592
pmid
36407421
authors array · 10 items
[0]
Jiahe Wu
[1]
Huanhuan Cai
[2]
Zhe Lei
[3]
Chenze Li
[4]
Yushuang Hu
[5]
Tong Zhang
[6]
Haoyan Zhu
[7]
Yi Lu
[8]
Jianlei Cao
[9]
Xiaorong Hu
journal
Frontiers in cardiovascular medicine
year
2022
abstract
Background: Ferroptosis is a form of regulatory cell death (RCD) caused by iron-dependent lipid peroxidation. The role of ferroptosis in the process of acute myocardial infarction (AMI) is still unclear and requires further study. Therefore, it is helpful to identify ferroptosis related genes (FRGs) involved in AMI and explore their expression patterns and molecular mechanisms. Methods: The AMI-related microarray datasets GSE66360 and GSE61144 were obtained using the Gene Expression Omnibus (GEO) online database. GO annotation, KEGG pathway enrichment analysis and Protein-protein interaction (PPI) analysis were performed for the common significant differential expression genes (CoDEGs) in these two datasets. The FRGs were obtained from the FerrDb V2 and the differentially expressed FRGs were used to identify potential biomarkers by receiver operating characteristic (ROC) analysis. The expression of these FRGs was verified using external dataset GSE60993 and GSE775. Finally, the expression of these FRGs was further verified in myocardial hypoxia model. Results: A total of 131 CoDEGs were identified and these genes were mainly enriched in the pathways of "inflammatory response," "immune response," "plasma membrane," "receptor activity," "protein homodimerization activity," "calcium ion binding," "Phagosome," "Cytokine-cytokine receptor interaction," and "Toll-like receptor signaling pathway." The top 7 hub genes ITGAM, S100A12, S100A9, TLR2, TLR4, TLR8, and TREM1 were identified from the PPI network. 45 and 14 FRGs were identified in GSE66360 and GSE61144, respectively. FRGs ACSL1, ATG7, CAMKK2, GABARAPL1, KDM6B, LAMP2, PANX2, PGD, PTEN, SAT1, STAT3, TLR4, and ZFP36 were significantly differentially expressed in external dataset GSE60993 with AUC ≥ 0.7. Finally, ALOX5, CAMKK2, KDM6B, LAMP2, PTEN, PTGS2, and ULK1 were identified as biomarkers of AMI based on the time-gradient transcriptome dataset of AMI mice and the cellular hypoxia model. Conclusion: In this study, based on the existing datasets, we identified differentially expressed FRGs in blood samples from patients with AMI and further validated these FRGs in the mouse time-gradient transcriptome dataset of AMI and the cellular hypoxia model. This study explored the expression pattern and molecular mechanism of FRGs in AMI, providing a basis for the accurate diagnosis of AMI and the selection of new therapeutic targets.
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GEO2R2 was used to perform the preliminary differential expression analysis. Benjamini-Hochberg method was used to correct adj. P for potential false positive results and adj. P-value < 0.05 and | logFC| > 0.8 was set as the cut-off criteria of DEGs.
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methodological
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sections[4] "Differential expression analysis" paragraph 2
quote
GEO2R2 was used to perform the preliminary differential expression analysis. Benjamini-Hochberg method was used to correct adj. P for potential false positive results and adj. P-value < 0.05 and | logFC| > 0.8 was set as the cut-off criteria of DEGs.
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complete
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.
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methodological
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sections[26] "Data availability statement" paragraph 2
quote
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.
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complete
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Finally, ALOX5, CAMKK2, KDM6B, LAMP2, PTEN, PTGS2, and ULK1 were identified as biomarkers of AMI based on the time-gradient transcriptome dataset of AMI mice and the cellular hypoxia model.
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qualitative
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null
evidence array · 1 item
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sections[0] "Abstract" paragraph 3
quote
Finally, ALOX5, CAMKK2, KDM6B, LAMP2, PTEN, PTGS2, and ULK1 were identified as biomarkers of AMI based on the time-gradient transcriptome dataset of AMI mice and the cellular hypoxia model.
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complete
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Finally, ALOX5, CAMKK2, KDM6B, LAMP2, PTEN, PTGS2, and ULK1 were identified as biomarkers of AMI based on the time-gradient transcriptome dataset of AMI mice and the cellular hypoxia model.
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The claim, method and evidence span published with the source article.
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the published estimate and its evidence
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Apply the paper's statistical method to the resolved series and compare the result with the published target.
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https://doi.org/10.3389/fcvm.2022.993592
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10.3389/fcvm.2022.993592
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PMC9669064
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.
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GEO
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GEO accession URL
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.
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GSM1495313
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33
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6884
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Homo sapiens
title
Assessment and Diagnostic Relevance of Novel Serum Biomarkers for Early Decision of ST-elevation Myocardial Infarction
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2026-11-01T15:39:55Z
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[2] object · 15 fields
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data:geo:GSE61144
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE61144
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null
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null
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null
note
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.
structure object · 15 fields
repository
GEO
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GEO accession URL
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The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.
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GSM1498388
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GSM1498389
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GSM1498390
[22]
GSM1498391
[23]
GSM1498392
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24
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null
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null
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6106
taxon
Homo sapiens
title
Expression data from blood samples of STEMI and Same STEMI patients after PIC
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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false
licence_read
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[3] object · 15 fields
id
data:geo:GSE66360
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raw
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE66360
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null
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null
access
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reader_required
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GSE66360
version
null
note
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.
structure object · 15 fields
repository
GEO
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GEO accession URL
access_statement_verbatim
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.
access_statement_kind
data_availability_statement
sample_accessions array · 99 items
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GSM1620819
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GSM1620820
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GSM1620823
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GSM1620824
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GSM1620825
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GSM1620826
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GSM1620827
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GSM1620828
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GSM1620829
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GSM1620830
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GSM1620831
[13]
GSM1620832
[14]
GSM1620833
[15]
GSM1620834
[16]
GSM1620835
[17]
GSM1620836
[18]
GSM1620837
[19]
GSM1620838
[20]
GSM1620839
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GSM1620840
[22]
GSM1620841
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GSM1620842
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GSM1620843
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GSM1620844
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GSM1620845
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GSM1620846
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GSM1620847
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GSM1620848
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GSM1620849
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GSM1620850
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GSM1620851
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GSM1620852
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GSM1620853
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GSM1620854
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GSM1620855
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GSM1620856
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GSM1620857
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GSM1620859
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GSM1620860
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GSM1620862
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GSM1620863
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GSM1620872
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GSM1620873
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GSM1620875
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GSM1620878
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GSM1620917
sample_count
99
group_sizes
null
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null
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570
taxon
Homo sapiens
title
A Whole Blood Molecular Signature for the Identification of Acute Myocardial Infarction Without Relying Upon Myonecrosis (microarray)
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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false
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[4] object · 15 fields
id
data:geo:GSE775
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE775
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null
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null
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identifier
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null
note
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.
structure object · 15 fields
repository
GEO
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GEO accession URL
access_statement_verbatim
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.
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data_availability_statement
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59
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null
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null
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81
taxon
Mus musculus
title
Mouse model of myocardial infarction
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2026-11-01T15:39:55Z
resolution_check
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false
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[0]
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[5]
asset:data:geo:GSE66360 licence not read
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asset:data:geo:GSE775 not downloaded
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asset:data:geo:GSE775 licence not read
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partial
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[0] object · 10 fields
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[0]
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[1]
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[2]
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method-2
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Network / pathway analysis
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[0]
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pathway enrichment
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GEO2R differential expression analysis with Benjamini-Hochberg correction, followed by receiver operating characteristic analysis
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evidence object · 3 fields
score
1
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quote
GEO2R2 was used to perform the preliminary differential expression analysis. Benjamini-Hochberg method was used to correct adj. P for potential false positive results and adj. P-value < 0.05 and | logFC| > 0.8 was set as the cut-off criteria of DEGs.
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[0]
method.reader_named_unmapped
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complete
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[0] object · 6 fields
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capability:computational_analysis
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[0]
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[1]
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[3]
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Automated Assays Laravel application and simulated adapters
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nothing:replicable_now
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owned
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tier
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[0]
GSE66360
[1]
GSE61144
[2]
GSE60993
[3]
GSE775
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[0]
GSE66360
[1]
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GSE60993
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GSE775
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[0]
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.
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The paper names GSE66360, GSE61144, GSE60993, GSE775 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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source:pmid:36407421
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lecular mechanisms. Methods: The AMI-related microarray datasets GSE66360 and GSE61144 were obtained
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biomarkers of AMI based on the time-gradient transcriptome dataset of AMI mice and the cellular hypoxia
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idated these FRGs in the mouse time-gradient transcriptome dataset of AMI and the cellular hypoxia mode
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ntially expressed FRGs in blood samples from patients with AMI and further validated these FRGs in the
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identified differentially expressed FRGs in blood samples from patients with AMI and further validated thes
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ts with AMI and further validated these FRGs in the mouse time-gradient transcriptome dataset of AMI a
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AMI and further validated these FRGs in the mouse time-gradient transcriptome dataset of AMI a
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ry Table 2The primer sequence information of qPCR experiment.Click here for additional data fi
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36407421", "kind": "science-record", "revision": 3, "content_hash": "sha256:56365272382b4c895bafca1b0a889e030b62d1335c8f16a9ca624108c26f5c2c", "created_at": "2026-11-01T19:00:52Z", "updated_at": "2026-11-01T22:08:08Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Expression pattern and diagnostic value of ferroptosis-related genes in acute myocardial infarction.", "doi": "10.3389/fcvm.2022.993592", "pmid": "36407421", "authors": ["Jiahe Wu", "Huanhuan Cai", "Zhe Lei", "Chenze Li", "Yushuang Hu", "Tong Zhang", "Haoyan Zhu", "Yi Lu", "Jianlei Cao", "Xiaorong Hu"], "journal": "Frontiers in cardiovascular medicine", "year": 2022, "abstract": "Background: Ferroptosis is a form of regulatory cell death (RCD) caused by iron-dependent lipid peroxidation. The role of ferroptosis in the process of acute myocardial infarction (AMI) is still unclear and requires further study. Therefore, it is helpful to identify ferroptosis related genes (FRGs) involved in AMI and explore their expression patterns and molecular mechanisms.\nMethods: The AMI-related microarray datasets GSE66360 and GSE61144 were obtained using the Gene Expression Omnibus (GEO) online database. GO annotation, KEGG pathway enrichment analysis and Protein-protein interaction (PPI) analysis were performed for the common significant differential expression genes (CoDEGs) in these two datasets. The FRGs were obtained from the FerrDb V2 and the differentially expressed FRGs were used to identify potential biomarkers by receiver operating characteristic (ROC) analysis. The expression of these FRGs was verified using external dataset GSE60993 and GSE775. Finally, the expression of these FRGs was further verified in myocardial hypoxia model.\nResults: A total of 131 CoDEGs were identified and these genes were mainly enriched in the pathways of \"inflammatory response,\" \"immune response,\" \"plasma membrane,\" \"receptor activity,\" \"protein homodimerization activity,\" \"calcium ion binding,\" \"Phagosome,\" \"Cytokine-cytokine receptor interaction,\" and \"Toll-like receptor signaling pathway.\" The top 7 hub genes ITGAM, S100A12, S100A9, TLR2, TLR4, TLR8, and TREM1 were identified from the PPI network. 45 and 14 FRGs were identified in GSE66360 and GSE61144, respectively. FRGs ACSL1, ATG7, CAMKK2, GABARAPL1, KDM6B, LAMP2, PANX2, PGD, PTEN, SAT1, STAT3, TLR4, and ZFP36 were significantly differentially expressed in external dataset GSE60993 with AUC ≥ 0.7. Finally, ALOX5, CAMKK2, KDM6B, LAMP2, PTEN, PTGS2, and ULK1 were identified as biomarkers of AMI based on the time-gradient transcriptome dataset of AMI mice and the cellular hypoxia model.\nConclusion: In this study, based on the existing datasets, we identified differentially expressed FRGs in blood samples from patients with AMI and further validated these FRGs in the mouse time-gradient transcriptome dataset of AMI and the cellular hypoxia model. This study explored the expression pattern and molecular mechanism of FRGs in AMI, providing a basis for the accurate diagnosis of AMI and the selection of new therapeutic targets.", "claims": [{"id": "claim-method", "statement": "GEO2R2 was used to perform the preliminary differential expression analysis. Benjamini-Hochberg method was used to correct adj. P for potential false positive results and adj. P-value < 0.05 and | logFC| > 0.8 was set as the cut-off criteria of DEGs.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36407421", "locator": "sections[4] \"Differential expression analysis\" paragraph 2", "quote": "GEO2R2 was used to perform the preliminary differential expression analysis. Benjamini-Hochberg method was used to correct adj. P for potential false positive results and adj. P-value < 0.05 and | logFC| > 0.8 was set as the cut-off criteria of DEGs."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36407421", "locator": "sections[26] \"Data availability statement\" paragraph 2", "quote": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Finally, ALOX5, CAMKK2, KDM6B, LAMP2, PTEN, PTGS2, and ULK1 were identified as biomarkers of AMI based on the time-gradient transcriptome dataset of AMI mice and the cellular hypoxia model.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:36407421", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "Finally, ALOX5, CAMKK2, KDM6B, LAMP2, PTEN, PTGS2, and ULK1 were identified as biomarkers of AMI based on the time-gradient transcriptome dataset of AMI mice and the cellular hypoxia model."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Finally, ALOX5, CAMKK2, KDM6B, LAMP2, PTEN, PTGS2, and ULK1 were identified as biomarkers of AMI based on the time-gradient transcriptome dataset of AMI mice and the cellular hypoxia model.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:36407421"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R1", "reachable": true, "accessions": ["GSE66360", "GSE61144", "GSE60993", "GSE775"], "resolved_accessions": ["GSE66360", "GSE61144", "GSE60993", "GSE775"], "statements": ["The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary material."], "basis": "The paper names GSE66360, GSE61144, GSE60993, GSE775 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. 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