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pmid:38046810

Identification of immunological characterization and Anoikis-related molecular clusters in rheumatoid arthritis.

Jianan Zhao · Kai Wei · Yiming Shi · Ping Jiang · Lingxia Xu · Cen Chang · Linshuai Xu · Yixin Zheng · Yu Shan · Jia Liu · Li Li · Shicheng Guo · Steven J Schrodi · Rongsheng Wang · Dongyi He

Frontiers in molecular biosciences · 2023 doi:10.3389/fmolb.2023.1202371

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complete

Experiment

partial

Data

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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:38046810
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2026-11-01T19:02:59Z
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title
Identification of immunological characterization and Anoikis-related molecular clusters in rheumatoid arthritis.
doi
10.3389/fmolb.2023.1202371
pmid
38046810
authors array · 15 items
[0]
Jianan Zhao
[1]
Kai Wei
[2]
Yiming Shi
[3]
Ping Jiang
[4]
Lingxia Xu
[5]
Cen Chang
[6]
Linshuai Xu
[7]
Yixin Zheng
[8]
Yu Shan
[9]
Jia Liu
[10]
Li Li
[11]
Shicheng Guo
[12]
Steven J Schrodi
[13]
Rongsheng Wang
[14]
Dongyi He
journal
Frontiers in molecular biosciences
year
2023
abstract
Objective: To investigate the potential association between Anoikis-related genes, which are responsible for preventing abnormal cellular proliferation, and rheumatoid arthritis (RA). Methods: Datasets GSE89408, GSE198520, and GSE97165 were obtained from the GEO with 282 RA patients and 28 healthy controls. We performed differential analysis of all genes and HLA genes. We performed a protein-protein interaction network analysis and identified hub genes based on STRING and cytoscape. Consistent clustering was performed with subgrouping of the disease. SsGSEA were used to calculate immune cell infiltration. Spearman's correlation analysis was employed to identify correlations. Enrichment scores of the GO and KEGG were calculated with the ssGSEA algorithm. The WGCNA and the DGIdb database were used to mine hub genes' interactions with drugs. Results: There were 26 differentially expressed Anoikis-related genes (FDR = 0.05, log2FC = 1) and HLA genes exhibited differential expression (P < 0.05) between the disease and control groups. Protein-protein interaction was observed among differentially expressed genes, and the correlation between PIM2 and RAC2 was found to be the highest; There were significant differences in the degree of immune cell infiltration between most of the immune cell types in the disease group and normal controls (P < 0.05). Anoikis-related genes were highly correlated with HLA genes. Based on the expression of Anoikis-related genes, RA patients were divided into two disease subtypes (cluster1 and cluster2). There were 59 differentially expressed Anoikis-related genes found, which exhibited significant differences in functional enrichment, immune cell infiltration degree, and HLA gene expression (P < 0.05). Cluster2 had significantly higher levels in all aspects than cluster1 did. The co-expression network analysis showed that cluster1 had 51 hub differentially expressed genes and cluster2 had 72 hub differentially expressed genes. Among them, three hub genes of cluster1 were interconnected with 187 drugs, and five hub genes of cluster2 were interconnected with 57 drugs. Conclusion: Our study identified a link between Anoikis-related genes and RA, and two distinct subtypes of RA were determined based on Anoikis-related gene expression. Notably, cluster2 may represent a more severe state of RA.
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Based on the merged data of rheumatoid arthritis, the R package WGCNA was used to construct a weight co-expression network.
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sections[16] "3.6 Identification of key molecules based on co-expression network analysis" paragraph 2
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Based on the merged data of rheumatoid arthritis, the R package WGCNA was used to construct a weight co-expression network.
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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.
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The co-expression network analysis showed that cluster1 had 51 hub differentially expressed genes and cluster2 had 72 hub differentially expressed genes.
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The co-expression network analysis showed that cluster1 had 51 hub differentially expressed genes and cluster2 had 72 hub differentially expressed genes.
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The co-expression network analysis showed that cluster1 had 51 hub differentially expressed genes and cluster2 had 72 hub differentially expressed genes.
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[1]
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[2]
pathway_enrich
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evidence object · 3 fields
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0.7
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medium
quote
protein-protein interaction
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id
method-4
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null
specific
null
label
WGCNA
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evidence object · 3 fields
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Based on the merged data of rheumatoid arthritis, the R package WGCNA was used to construct a weight co-expression network.
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method.reader_named_unmapped
[1]
method.group_comparison_wilcoxon
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complete
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capability_id
capability:computational_analysis
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pca
[5]
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gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
complete
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R1
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nothing:replicable_now
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tier
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missing_operations array · 1 item
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group_comparison_wilcoxon
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: wilcoxon.
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
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true
accessions array · 3 items
[0]
GSE89408
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GSE198520
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GSE97165
resolved_accessions array · 3 items
[0]
GSE89408
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GSE198520
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GSE97165
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.
basis
The paper names GSE89408, GSE198520, GSE97165 in GEO and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
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assets array · 2 items
[0]
source:pmid:38046810
[1]
data:geo:GSE198520
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group_comparison_wilcoxon
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null
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data:geo:GSE198520
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
2026-11-01T19:01:27Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
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5
usage object · 3 fields
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15684
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1262
cached_tokens
128
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[0] object · 4 fields
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extraction
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MiniMax-M3.1-Flash
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[2]
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absent
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null
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pmid:38046810
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paper
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pmid:38046810
[1] object · 3 fields
id
source:pmid:38046810
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manuscript
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PMID 38046810 full text
[2] object · 3 fields
id
data:geo:GSE198520
type
dataset
label
GEO GSE198520
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
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[0] object · 3 fields
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paper
label
pmid:38046810
[1] object · 3 fields
id
source:pmid:38046810
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manuscript
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PMID 38046810 full text
[2] object · 3 fields
id
data:geo:GSE198520
type
dataset
label
GEO GSE198520
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-38046810
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extraction
used array · 1 item
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agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE198520
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accession_resolution
used array · 1 item
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data:geo:GSE198520
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agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
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agent:corpus-assay-engine
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software
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agent:minimax-reader
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MiniMax literature reader
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dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
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lineage object · 4 fields
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assays array · 1 item
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dsl_catalogue
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38046810", "kind": "science-record", "revision": 4, "content_hash": "sha256:ff5b4019e6f229e0013995dc71cc0cde032d64e9df2ec327feb81a611429fa23", "created_at": "2026-11-01T19:02:59Z", "updated_at": "2026-11-01T22:10:48Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of immunological characterization and Anoikis-related molecular clusters in rheumatoid arthritis.", "doi": "10.3389/fmolb.2023.1202371", "pmid": "38046810", "authors": ["Jianan Zhao", "Kai Wei", "Yiming Shi", "Ping Jiang", "Lingxia Xu", "Cen Chang", "Linshuai Xu", "Yixin Zheng", "Yu Shan", "Jia Liu", "Li Li", "Shicheng Guo", "Steven J Schrodi", "Rongsheng Wang", "Dongyi He"], "journal": "Frontiers in molecular biosciences", "year": 2023, "abstract": "Objective: To investigate the potential association between Anoikis-related genes, which are responsible for preventing abnormal cellular proliferation, and rheumatoid arthritis (RA). Methods: Datasets GSE89408, GSE198520, and GSE97165 were obtained from the GEO with 282 RA patients and 28 healthy controls. We performed differential analysis of all genes and HLA genes. We performed a protein-protein interaction network analysis and identified hub genes based on STRING and cytoscape. Consistent clustering was performed with subgrouping of the disease. SsGSEA were used to calculate immune cell infiltration. Spearman's correlation analysis was employed to identify correlations. Enrichment scores of the GO and KEGG were calculated with the ssGSEA algorithm. The WGCNA and the DGIdb database were used to mine hub genes' interactions with drugs. Results: There were 26 differentially expressed Anoikis-related genes (FDR = 0.05, log2FC = 1) and HLA genes exhibited differential expression (P < 0.05) between the disease and control groups. Protein-protein interaction was observed among differentially expressed genes, and the correlation between PIM2 and RAC2 was found to be the highest; There were significant differences in the degree of immune cell infiltration between most of the immune cell types in the disease group and normal controls (P < 0.05). Anoikis-related genes were highly correlated with HLA genes. Based on the expression of Anoikis-related genes, RA patients were divided into two disease subtypes (cluster1 and cluster2). There were 59 differentially expressed Anoikis-related genes found, which exhibited significant differences in functional enrichment, immune cell infiltration degree, and HLA gene expression (P < 0.05). Cluster2 had significantly higher levels in all aspects than cluster1 did. The co-expression network analysis showed that cluster1 had 51 hub differentially expressed genes and cluster2 had 72 hub differentially expressed genes. Among them, three hub genes of cluster1 were interconnected with 187 drugs, and five hub genes of cluster2 were interconnected with 57 drugs. Conclusion: Our study identified a link between Anoikis-related genes and RA, and two distinct subtypes of RA were determined based on Anoikis-related gene expression. Notably, cluster2 may represent a more severe state of RA.", "claims": [{"id": "claim-method", "statement": "Based on the merged data of rheumatoid arthritis, the R package WGCNA was used to construct a weight co-expression network.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38046810", "locator": "sections[16] \"3.6 Identification of key molecules based on co-expression network analysis\" paragraph 2", "quote": "Based on the merged data of rheumatoid arthritis, the R package WGCNA was used to construct a weight co-expression network."}], "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.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38046810", "locator": "sections[20] \"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."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The co-expression network analysis showed that cluster1 had 51 hub differentially expressed genes and cluster2 had 72 hub differentially expressed genes.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:38046810", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The co-expression network analysis showed that cluster1 had 51 hub differentially expressed genes and cluster2 had 72 hub differentially expressed genes."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": "The co-expression network analysis showed that cluster1 had 51 hub differentially expressed genes and cluster2 had 72 hub differentially expressed genes.", "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:38046810"], "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. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE198520"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "blocked", "blocked_on": "method:group_comparison_wilcoxon", "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE198520"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": ["step:run_analysis blocked on method:group_comparison_wilcoxon"]}, "data": {"state": "partial", "assets": [{"id": "source:pmid:38046810", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": 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