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pmid:38739634

Identification of potential biomarkers of leprosy: A study based on GEO datasets.

Qun Zhou · Ping Shi · Wei Dong Shi · Jun Gao · Yi Chen Wu · Jing Wan · Li Li Yan · Yi Zheng

PloS one · 2024 doi:10.1371/journal.pone.0302753

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

Execution evidence has not yet been added to this .science file. Explore its methods, data and open questions to plan the next step.
Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:38739634
kind
science-record
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sha256:e194f9c964601ecfdc84715f12b63591d6d68ba77844f7ef3d088ad90206f4a1
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https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
created_at
2026-11-01T19:20:42Z
updated_at
2026-11-01T22:11:51Z
generator object · 2 fields
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corpus-assay-engine
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paper object · 10 fields
state
complete
title
Identification of potential biomarkers of leprosy: A study based on GEO datasets.
doi
10.1371/journal.pone.0302753
pmid
38739634
authors array · 8 items
[0]
Qun Zhou
[1]
Ping Shi
[2]
Wei Dong Shi
[3]
Jun Gao
[4]
Yi Chen Wu
[5]
Jing Wan
[6]
Li Li Yan
[7]
Yi Zheng
journal
PloS one
year
2024
abstract
Leprosy has a high rate of cripplehood and lacks available early effective diagnosis methods for prevention and treatment, thus novel effective molecule markers are urgently required. In this study, we conducted bioinformatics analysis with leprosy and normal samples acquired from the GEO database(GSE84893, GSE74481, GSE17763, GSE16844 and GSE443). Through WGCNA analysis, 85 hub genes were screened(GS > 0.7 and MM > 0.8). Through DEG analysis, 82 up-regulated and 3 down-regulated genes were screened(|Log2FC| > 3 and FDR < 0.05). Then 49 intersection genes were considered as crucial and subjected to GO annotation, KEGG pathway and PPI analysis to determine the biological significance in the pathogenesis of leprosy. Finally, we identified a gene-pathway network, suggesting ITK, CD48, IL2RG, CCR5, FGR, JAK3, STAT1, LCK, PTPRC, CXCR4 can be used as biomarkers and these genes are active in 6 immune system pathways, including Chemokine signaling pathway, Th1 and Th2 cell differentiation, Th17 cell differentiation, T cell receptor signaling pathway, Natural killer cell mediated cytotoxicity and Leukocyte transendothelial migration. We identified 10 crucial gene markers and related important pathways that acted as essential components in the etiology of leprosy. Our study provides potential targets for diagnostic biomarkers and therapy of leprosy.
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Weighted Gene Co-expression Network Analysis(WGCNA) was constructed on the normalized gene expression profiles with R package “WGCNA” [18].
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sections[5] "WGCNA analysis" paragraph 2
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Weighted Gene Co-expression Network Analysis(WGCNA) was constructed on the normalized gene expression profiles with R package “WGCNA” [18].
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sections[19] "Data Availability" paragraph 2
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All relevant data are within the paper and its supporting information files.
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The study identified 10 candidate gene biomarkers and six related immune-system pathways for leprosy.
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sections[0] "Abstract" paragraph 1
quote
We identified 10 crucial gene markers and related important pathways that acted as essential components in the etiology of leprosy.
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complete
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experiment object · 8 fields
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complete
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The study identified 10 candidate gene biomarkers and six related immune-system pathways for leprosy.
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the published estimate and its evidence
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null
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570
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title
Integrated pathways for neutrophil recruitment and inflammation in leprosy
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2026-11-01T20:16:08Z
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570
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Divergence of macrophage phagocytic and antimicrobial programs in leprosy
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2026-11-01T20:16:08Z
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null
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null
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All relevant data are within the paper and its supporting information files.
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All relevant data are within the paper and its supporting information files.
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[0]
GSM6766
[1]
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[2]
GSM6768
[3]
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GSM6770
[5]
GSM6771
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GSM6772
[7]
GSM6773
[8]
GSM6774
[9]
GSM6775
[10]
GSM6776
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11
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null
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null
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8300
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Homo sapiens
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Leprosy lesion gene expression
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2026-11-01T20:16:08Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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null
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null
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null
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GSM1921384
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GSM1921385
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GSM1921386
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GSM1921388
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GSM1921389
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GSM1921390
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GSM1921392
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GSM1921395
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GSM1921396
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GSM1921401
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GSM1921402
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GSM1921403
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GSM1921404
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GSM1921405
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GSM1921406
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GSM1921407
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GSM1921409
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GSM1921410
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GSM1921411
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GSM1921412
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GSM1921413
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GSM1921414
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GSM1921415
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GSM1921416
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GSM1921417
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GSM1921419
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GSM1921420
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GSM1921421
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GSM1921422
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GSM1921423
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GSM1921424
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GSM1921425
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GSM1921426
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GSM1921427
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GSM1921428
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GSM1921429
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GSM1921430
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GSM1921431
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GSM1921432
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GSM1921433
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GSM1921434
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GSM1921435
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GSM1921436
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GSM1921437
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GSM1921440
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GSM1921443
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GSM1921444
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GSM1921445
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GSM1921449
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GSM1921450
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GSM1921451
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GSM1921452
sample_count
76
group_sizes
null
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null
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14550
taxon
Homo sapiens
title
Genome-wide screening of mRNA expression in leprosy patients
resolution_checked_at
2026-11-01T20:16:08Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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data:geo:GSE84893
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All relevant data are within the paper and its supporting information files.
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All relevant data are within the paper and its supporting information files.
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GSM2253651
[5]
GSM2253652
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6
group_sizes
null
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null
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570
taxon
Homo sapiens
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Integration of cell type deconvolution with immune pathways identifies gene networks of host defense and immunopathology in leprosy
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2026-11-01T20:16:08Z
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38739634", "kind": "science-record", "revision": 4, "content_hash": "sha256:e194f9c964601ecfdc84715f12b63591d6d68ba77844f7ef3d088ad90206f4a1", "created_at": "2026-11-01T19:20:42Z", "updated_at": "2026-11-01T22:11:51Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of potential biomarkers of leprosy: A study based on GEO datasets.", "doi": "10.1371/journal.pone.0302753", "pmid": "38739634", "authors": ["Qun Zhou", "Ping Shi", "Wei Dong Shi", "Jun Gao", "Yi Chen Wu", "Jing Wan", "Li Li Yan", "Yi Zheng"], "journal": "PloS one", "year": 2024, "abstract": "Leprosy has a high rate of cripplehood and lacks available early effective diagnosis methods for prevention and treatment, thus novel effective molecule markers are urgently required. In this study, we conducted bioinformatics analysis with leprosy and normal samples acquired from the GEO database(GSE84893, GSE74481, GSE17763, GSE16844 and GSE443). Through WGCNA analysis, 85 hub genes were screened(GS > 0.7 and MM > 0.8). Through DEG analysis, 82 up-regulated and 3 down-regulated genes were screened(|Log2FC| > 3 and FDR < 0.05). Then 49 intersection genes were considered as crucial and subjected to GO annotation, KEGG pathway and PPI analysis to determine the biological significance in the pathogenesis of leprosy. Finally, we identified a gene-pathway network, suggesting ITK, CD48, IL2RG, CCR5, FGR, JAK3, STAT1, LCK, PTPRC, CXCR4 can be used as biomarkers and these genes are active in 6 immune system pathways, including Chemokine signaling pathway, Th1 and Th2 cell differentiation, Th17 cell differentiation, T cell receptor signaling pathway, Natural killer cell mediated cytotoxicity and Leukocyte transendothelial migration. We identified 10 crucial gene markers and related important pathways that acted as essential components in the etiology of leprosy. Our study provides potential targets for diagnostic biomarkers and therapy of leprosy.", "claims": [{"id": "claim-method", "statement": "Weighted Gene Co-expression Network Analysis(WGCNA) was constructed on the normalized gene expression profiles with R package “WGCNA” [18].", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38739634", "locator": "sections[5] \"WGCNA analysis\" paragraph 2", "quote": "Weighted Gene Co-expression Network Analysis(WGCNA) was constructed on the normalized gene expression profiles with R package “WGCNA” [18]."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All relevant data are within the paper and its supporting information files.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38739634", "locator": "sections[19] \"Data Availability\" paragraph 2", "quote": "All relevant data are within the paper and its supporting information files."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The study identified 10 candidate gene biomarkers and six related immune-system pathways for leprosy.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:38739634", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "We identified 10 crucial gene markers and related important pathways that acted as essential components in the etiology of leprosy."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The study identified 10 candidate gene biomarkers and six related immune-system pathways for leprosy.", "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:38739634"], "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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