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pmid:39148085

Identification of HTRA1, DPT and MXRA5 as potential biomarkers associated with osteoarthritis progression and immune infiltration.

Yunchao Sun · Hui Yang · Jiaquan Guo · Jian Du · Shoujiang Han · Xinming Yang

BMC musculoskeletal disorders · 2024 doi:10.1186/s12891-024-07758-7

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:39148085
kind
science-record
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sha256:1c27cefe412dd4fa860cb6232af3bd057df1ee5a3c329a65bf593d3670868f49
schema
https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T20:29:16Z
updated_at
2026-11-01T21:33:43Z
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paper object · 10 fields
state
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title
Identification of HTRA1, DPT and MXRA5 as potential biomarkers associated with osteoarthritis progression and immune infiltration.
doi
10.1186/s12891-024-07758-7
pmid
39148085
authors array · 6 items
[0]
Yunchao Sun
[1]
Hui Yang
[2]
Jiaquan Guo
[3]
Jian Du
[4]
Shoujiang Han
[5]
Xinming Yang
journal
BMC musculoskeletal disorders
year
2024
abstract
BACKGROUND: Our study aimed to identify potential specific biomarkers for osteoarthritis (OA) and assess their relationship with immune infiltration. METHODS: We utilized data from GSE117999, GSE51588, and GSE57218 as training sets, while GSE114007 served as a validation set, all obtained from the GEO database. First, weighted gene co-expression network analysis (WGCNA) and functional enrichment analysis were performed to identify hub modules and potential functions of genes. We subsequently screened for potential OA biomarkers within the differentially expressed genes (DEGs) of the hub module using machine learning methods. The diagnostic accuracy of the candidate genes was validated. Additionally, single gene analysis and ssGSEA was performed. Then, we explored the relationship between biomarkers and immune cells. Lastly, we employed RT-PCR to validate our results. RESULTS: WGCNA results suggested that the blue module was the most associated with OA and was functionally associated with extracellular matrix (ECM)-related terms. Our analysis identified ALB, HTRA1, DPT, MXRA5, CILP, MPO, and PLAT as potential biomarkers. Notably, HTRA1, DPT, and MXRA5 consistently exhibited increased expression in OA across both training and validation cohorts, demonstrating robust diagnostic potential. The ssGSEA results revealed that abnormal infiltration of DCs, NK cells, Tfh, Th2, and Treg cells might contribute to OA progression. HTRA1, DPT, and MXRA5 showed significant correlation with immune cell infiltration. The RT-PCR results also confirmed these findings. CONCLUSIONS: HTRA1, DPT, and MXRA5 are promising biomarkers for OA. Their overexpression strongly correlates with OA progression and immune cell infiltration.
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A gene co-expression network was established using the WGCNA R package with normalized expression data for 16,106 genes in the training set [12].
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sections[4] "WGCNA analysis and module selection" paragraph 2
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A gene co-expression network was established using the WGCNA R package with normalized expression data for 16,106 genes in the training set [12].
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sections[25] "Data availability" paragraph 2
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The data used for analysis in our study are available from GEO database.
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WGCNA identified the blue module as the module most strongly associated with osteoarthritis (R = 0.37, P = 6e-06).
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As shown in Fig. 1C, the blue module showed the strongest association with OA (R = 0.37, P = 6e-06).
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sections[13] "Identification of the key module and enrichment analysis" paragraph 2
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As shown in Fig. 1C, the blue module showed the strongest association with OA (R = 0.37, P = 6e-06).
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WGCNA identified the blue module as the module most strongly associated with osteoarthritis (R = 0.37, P = 6e-06).
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Identification of transcription factors responsible for dysregulated networks in human osteoarthritis cartilage by global gene expression analysis
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Transcriptome comparison of cartilage from patients with and without osteoarthritis
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Homo sapiens
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Genome-wide Expression Profiles of Subchondral Bone in Osteoarthritis
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Gene expression profiles from joint-matched macroscopically intact and OA affected cartilage of patients undergoing joint replacement surgery due to end-stage OA
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A gene co-expression network was established using the WGCNA R package with normalized expression data for 16,106 genes in the training set [12].
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[1]
asset:data:geo:GSE114007 not downloaded
[2]
asset:data:geo:GSE117999 licence not read
[3]
asset:data:geo:GSE117999 not downloaded
[4]
asset:data:geo:GSE51588 licence not read
[5]
asset:data:geo:GSE51588 not downloaded
[6]
asset:data:geo:GSE57218 licence not read
[7]
asset:data:geo:GSE57218 not downloaded
[8]
execution.not_run
[9]
method.reader_named_unmapped
[10]
review.human_critique
[11]
review.independent_reader
[12]
review.machine_critique
Complete file
{"sci_version": "1.0", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39148085", "kind": "science-record", "revision": 2, "content_hash": "sha256:1c27cefe412dd4fa860cb6232af3bd057df1ee5a3c329a65bf593d3670868f49", "created_at": "2026-11-01T20:29:16Z", "updated_at": "2026-11-01T21:33:43Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of HTRA1, DPT and MXRA5 as potential biomarkers associated with osteoarthritis progression and immune infiltration.", "doi": "10.1186/s12891-024-07758-7", "pmid": "39148085", "authors": ["Yunchao Sun", "Hui Yang", "Jiaquan Guo", "Jian Du", "Shoujiang Han", "Xinming Yang"], "journal": "BMC musculoskeletal disorders", "year": 2024, "abstract": "BACKGROUND: Our study aimed to identify potential specific biomarkers for osteoarthritis (OA) and assess their relationship with immune infiltration.\nMETHODS: We utilized data from GSE117999, GSE51588, and GSE57218 as training sets, while GSE114007 served as a validation set, all obtained from the GEO database. First, weighted gene co-expression network analysis (WGCNA) and functional enrichment analysis were performed to identify hub modules and potential functions of genes. We subsequently screened for potential OA biomarkers within the differentially expressed genes (DEGs) of the hub module using machine learning methods. The diagnostic accuracy of the candidate genes was validated. Additionally, single gene analysis and ssGSEA was performed. Then, we explored the relationship between biomarkers and immune cells. Lastly, we employed RT-PCR to validate our results.\nRESULTS: WGCNA results suggested that the blue module was the most associated with OA and was functionally associated with extracellular matrix (ECM)-related terms. Our analysis identified ALB, HTRA1, DPT, MXRA5, CILP, MPO, and PLAT as potential biomarkers. Notably, HTRA1, DPT, and MXRA5 consistently exhibited increased expression in OA across both training and validation cohorts, demonstrating robust diagnostic potential. The ssGSEA results revealed that abnormal infiltration of DCs, NK cells, Tfh, Th2, and Treg cells might contribute to OA progression. HTRA1, DPT, and MXRA5 showed significant correlation with immune cell infiltration. The RT-PCR results also confirmed these findings.\nCONCLUSIONS: HTRA1, DPT, and MXRA5 are promising biomarkers for OA. 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE114007"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "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:GSE114007"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:39148085", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1186/s12891-024-07758-7", "sha256": 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"GSM1248807", "GSM1248808"], "sample_count": 50, "group_sizes": null, "group_sizes_basis": null, "platform": "13497", "taxon": "Homo sapiens", "title": "Genome-wide Expression Profiles of Subchondral Bone in Osteoarthritis", "resolution_checked_at": "2026-11-01T15:39:54Z", "resolution_check": "identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}, {"id": "data:geo:GSE57218", "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=GSE57218", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE57218", "version": null, "note": "The data used for analysis in our study are available from GEO database.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The data used for analysis in our study are available from 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