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pmid:41538664

Identification of anoikis-related biomarkers linking immune infiltration to acute myocardial infarction.

Yang Zhao · Shangfen Wang · Huiying Ji · Lihui Han · Shiai Wang · Xunli Yin · Qian Zhao

Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2026 doi:10.1590/1414-431X2025e14989

Paper

complete

Experiment

complete

Data

partial

Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:41538664
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2026-11-01T20:31:30Z
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2026-11-01T22:57:44Z
generator object · 2 fields
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paper object · 10 fields
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title
Identification of anoikis-related biomarkers linking immune infiltration to acute myocardial infarction.
doi
10.1590/1414-431X2025e14989
pmid
41538664
authors array · 7 items
[0]
Yang Zhao
[1]
Shangfen Wang
[2]
Huiying Ji
[3]
Lihui Han
[4]
Shiai Wang
[5]
Xunli Yin
[6]
Qian Zhao
journal
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica
year
2026
abstract
This study was designed to identify new biomarkers for early diagnosis of acute myocardial infarction (AMI). GSE66360 and GSE48060 datasets were downloaded from the Gene Expression Omnibus (GEO) database. The "limma" tool was used to screen differentially expressed genes (DEGs). A total of 557 anoikis-related genes (ARGs) were obtained from the GeneCard database. Differentially expressed ARGs (DEARGs) were obtained by intersecting DEGs with ARGs. The least absolute shrinkage and selection operator (LASSO), support vector machine (SVM), and Random Forest (RF) were used to screen the hub DEARGs. Real-time quantitative polymerase chain reaction (RT-qPCR) was used to determine the expression of hub DEARGs. A total of 21 DEARGs were obtained, all of which were up-regulated in AMI samples. Functional enrichment analysis showed that the DEARGs were mainly enriched in peptidase activity and extracellular matrix. Immune cell infiltration analysis revealed a significant difference in 14 immune cells between the AMI and normal groups. Nine feature risk genes, including ITPRIP, MMP9, NAMPT, CDKN1A, PLAUR, PLAU, SERPINA1, THBS1, and FN1 were screened by LASSO, SVM, and RF. The RT-qPCR analyses verified that the feature genes were up-regulated in AMI patients, which were basically consistent with the main bioinformatics analysis results. We also validated 9 hub DEARGs in the GSE48060 dataset and constructed a nomogram by integrating these DEARGs. This study analyzed the differential expression of ARGs and immune profiles in AMI and normal samples, screened 9 risk feature genes for predicting AMI, and provided a theoretical basis for the immunotherapy regimen of AMI.
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After the preparation of the GSE66360 dataset, data normalization was performed using the normalizeBetweenArrays function, followed by screening for differentially expressed genes (DEGs) with the “limma” package.
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sections[4] "Analysis of differentially expressed genes" paragraph 2
quote
After the preparation of the GSE66360 dataset, data normalization was performed using the normalizeBetweenArrays function, followed by screening for differentially expressed genes (DEGs) with the “limma” package.
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sections[23] "Data Availability Statement" paragraph 2
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All data generated or analyzed during this study are included in this published article.
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The limma-based analysis of GSE66360 and GSE48060 identified nine risk feature genes for predicting acute myocardial infarction.
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sections[0] "Abstract" paragraph 1
quote
The “limma” tool was used to screen differentially expressed genes (DEGs).
[1] object · 3 fields
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sections[0] "Abstract" paragraph 1
quote
Nine feature risk genes, including ITPRIP, MMP9, NAMPT, CDKN1A, PLAUR, PLAU, SERPINA1, THBS1, and FN1 were screened by LASSO, SVM, and RF.
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The limma-based analysis of GSE66360 and GSE48060 identified nine risk feature genes for predicting acute myocardial infarction.
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Transcriptome from circulating cells suggests dysregulated pathways associated with long-term recurrent events following first-time myocardial infarction.
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436
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null
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null
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6244
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Homo sapiens
title
Gene expression profiling reveals potential prognostic biomarkers associated with the progression of heart failure
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 · 15 fields
id
data:geo:GSE66360
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raw
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application/vnd.ncbi.geo-series+json
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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
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resolved
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null
reader_status
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GSE66360
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null
note
All data generated or analyzed during this study are included in this published article.
structure object · 15 fields
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GEO
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GEO accession URL
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All data generated or analyzed during this study are included in this published article.
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data_availability_statement
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sample_count
99
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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
licence_read
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gaps array · 6 items
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asset:data:geo:GSE59867 licence not read
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asset:data:geo:GSE66360 not downloaded
[5]
asset:data:geo:GSE66360 licence not read
analysis object · 4 fields
state
partial
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[0] object · 10 fields
id
method-1
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differential_expression
specific
limma_voom
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Differential expression analysis
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[0]
normalise_counts
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differential_expression_fit
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fdr_bh
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count_matrix_with_condition
evidence object · 3 fields
score
1
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quote
After the preparation of the GSE66360 dataset, data normalization was performed using the normalizeBetweenArrays function, followed by screening for differentially expressed genes (DEGs) with the “limma” package.
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id
method-2
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group_comparison
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Group comparison
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missing_operations array · 1 item
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student_t
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two_or_more_groups_continuous
evidence object · 3 fields
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0.8
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Student's t-test
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id
method-3
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machine_learning
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random_forest
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Machine learning
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missing_operations array · 1 item
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machine_learning_random_forest
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false
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labelled_feature_matrix
evidence object · 3 fields
score
0.7
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Random Forest
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machine_learning
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cross_validate
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labelled_feature_matrix
evidence object · 3 fields
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0.7
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support vector machine
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id
method-5
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network_analysis
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pathway_enrichment
label
Network / pathway analysis
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pathway_enrich
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edge_list
evidence object · 3 fields
score
0.8
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GO enrichment
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method.reader_differs_from_extractor
capability object · 3 fields
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complete
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[0] object · 6 fields
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capability:computational_analysis
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Computational analysis platform
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candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
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R1
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nothing:replicable_now
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: limma_voom.
capability object · 4 fields
tier
R1
capability_id
capability:computational_analysis
availability_state
owned
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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
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GSE66360
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GSE66360
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[0]
All data generated or analyzed during this study are included in this published article.
basis
The paper names GSE66360, GSE48060, GSE59867 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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run_analysis
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partial
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extraction_review
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MiniMax-M3.1-Flash
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minimax
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minimax
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single_reader
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verbatim
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verbatim
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extraction
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paper
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source:pmid:41538664
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GEO GSE48060
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time quantitative polymerase chain reaction (RT-qPCR) was used to determine the expression of hub
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[2]
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:41538664", "kind": "science-record", "revision": 4, "content_hash": "sha256:04e2e46258825ccc7a264a1b76743247cc78538dfd867d3b63fdb58b464da8b6", "created_at": "2026-11-01T20:31:30Z", "updated_at": "2026-11-01T22:57:44Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of anoikis-related biomarkers linking immune infiltration to acute myocardial infarction.", "doi": "10.1590/1414-431X2025e14989", "pmid": "41538664", "authors": ["Yang Zhao", "Shangfen Wang", "Huiying Ji", "Lihui Han", "Shiai Wang", "Xunli Yin", "Qian Zhao"], "journal": "Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica", "year": 2026, "abstract": "This study was designed to identify new biomarkers for early diagnosis of acute myocardial infarction (AMI). GSE66360 and GSE48060 datasets were downloaded from the Gene Expression Omnibus (GEO) database. The \"limma\" tool was used to screen differentially expressed genes (DEGs). A total of 557 anoikis-related genes (ARGs) were obtained from the GeneCard database. Differentially expressed ARGs (DEARGs) were obtained by intersecting DEGs with ARGs. The least absolute shrinkage and selection operator (LASSO), support vector machine (SVM), and Random Forest (RF) were used to screen the hub DEARGs. Real-time quantitative polymerase chain reaction (RT-qPCR) was used to determine the expression of hub DEARGs. A total of 21 DEARGs were obtained, all of which were up-regulated in AMI samples. Functional enrichment analysis showed that the DEARGs were mainly enriched in peptidase activity and extracellular matrix. Immune cell infiltration analysis revealed a significant difference in 14 immune cells between the AMI and normal groups. Nine feature risk genes, including ITPRIP, MMP9, NAMPT, CDKN1A, PLAUR, PLAU, SERPINA1, THBS1, and FN1 were screened by LASSO, SVM, and RF. The RT-qPCR analyses verified that the feature genes were up-regulated in AMI patients, which were basically consistent with the main bioinformatics analysis results. We also validated 9 hub DEARGs in the GSE48060 dataset and constructed a nomogram by integrating these DEARGs. 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