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pmid:36059959

Integrated bioinformatics analysis uncovers characteristic genes and molecular subtyping system for endometriosis.

Zhaowei Wang · Jia Liu · Miaoli Li · Lishan Lian · Xiaojie Cui · Tai-Wei Ng · Maoshu Zhu

Frontiers in pharmacology · 2022 doi:10.3389/fphar.2022.932526

Paper

complete

Experiment

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Data

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Analysis

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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:36059959
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science-record
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2026-11-01T18:15:15Z
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title
Integrated bioinformatics analysis uncovers characteristic genes and molecular subtyping system for endometriosis.
doi
10.3389/fphar.2022.932526
pmid
36059959
authors array · 7 items
[0]
Zhaowei Wang
[1]
Jia Liu
[2]
Miaoli Li
[3]
Lishan Lian
[4]
Xiaojie Cui
[5]
Tai-Wei Ng
[6]
Maoshu Zhu
journal
Frontiers in pharmacology
year
2022
abstract
Objective: Endometriosis is a chronic inflammatory estrogen-dependent disease with the growth of endometrial tissues outside the uterine cavity. Nevertheless, the etiology of endometriosis is still unclear. Integrated bioinformatics analysis was implemented to reveal the molecular mechanisms underlying this disease. Methods: A total of four gene expression datasets (GSE7305, GSE11691, GSE23339, and GSE25628) were retrieved from the GEO, which were merged into a meta-dataset, followed by the removal of batch effects via the sva package. Weighted gene co-expression network analysis (WGCNA) was implemented, and endometriosis-related genes were screened under normal and endometriosis conditions. Thereafter, characteristic genes were determined via Lasso analysis. The diagnostic performance was estimated via receiver operating characteristic curves, and epigenetic and post-transcriptional modifications were analyzed. Small molecular compounds were predicted. Unsupervised clustering analysis was conducted via non-negative matrix factorization algorithm. The enriched pathways were analyzed via gene set enrichment analysis or GSVA. Immune features were evaluated according to immune-checkpoints, HLA, receptors, chemokines, and immune cells. Results: In total, four characteristic genes (BGN, AQP1, ELMO1, and DDR2) were determined for endometriosis, all of which exhibited the favorable efficacy in diagnosing endometriosis. Their aberrant levels were modulated by epigenetic and post-transcriptional modifications. In total, 51 potential drugs were predicted against endometriosis. The characteristic genes exhibited remarkable associations with immunological function. Three subtypes were classified across endometriosis, with different mechanisms and immune features. Conclusion: Our study reveals the characteristic genes and novel molecular subtyping of endometriosis, contributing to the early diagnosis and intervention in endometriosis.
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Through Lasso Cox regression algorithm, over-fitting risk was minimized with the glmnet package. The alteration trajectory of each variable was assessed and 10-fold cross-validated.
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sections[6] "Screening characteristic genes" paragraph 2
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Through Lasso Cox regression algorithm, over-fitting risk was minimized with the glmnet package. The alteration trajectory of each variable was assessed and 10-fold cross-validated.
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sections[29] "Data availability statement" paragraph 2
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The AUCs (95%CI) of AQP1, BGN, DDR2, and ELMO1 were 0.96 (1.00–0.89), 0.98 (1.00–0.95), 1.00 (1.00–0.99), and 0.99 (1.00–0.98), respectively, demonstrating that each characteristic gene enabled to diagnose endometriosis accurately and sensitively (Figures 4D–G).
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The AUCs (95%CI) of AQP1, BGN, DDR2, and ELMO1 were 0.96 (1.00–0.89), 0.98 (1.00–0.95), 1.00 (1.00–0.99), and 0.99 (1.00–0.98), respectively, demonstrating that each characteristic gene enabled to diagnose endometriosis accurately and sensitively (Figures 4D–G).
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sections[17] "Identification of four characteristic genes in endometriosis" paragraph 2
quote
Through Lasso algorithm, four characteristic genes were determined among the shared endometriosis-related genes, containing BGN, AQP1, ELMO1, and DDR2 (Figures 4A,B).
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sections[17] "Identification of four characteristic genes in endometriosis" paragraph 2
quote
The AUCs (95%CI) of AQP1, BGN, DDR2, and ELMO1 were 0.96 (1.00–0.89), 0.98 (1.00–0.95), 1.00 (1.00–0.99), and 0.99 (1.00–0.98), respectively, demonstrating that each characteristic gene enabled to diagnose endometriosis accurately and sensitively (Figures 4D–G).
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The AUCs (95%CI) of AQP1, BGN, DDR2, and ELMO1 were 0.96 (1.00–0.89), 0.98 (1.00–0.95), 1.00 (1.00–0.99), and 0.99 (1.00–0.98), respectively, demonstrating that each characteristic gene enabled to diagnose endometriosis accurately and sensitively (Figures 4D–G).
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Differentially expressed genes in HEECs of eutopic endometrium of patients with endometriosis compared with control
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accession_resolution
used array · 1 item
[0]
data:geo:GSE11691
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
label
Corpus assay engine
[1] object · 3 fields
id
agent:minimax-reader
type
software
label
MiniMax literature reader
source_run_id
reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
2cb3e42f047d2ecf
snapshot_id
ba34b49490d9bfaf
lineage object · 4 fields
parent_id
pmid:36059959
parent_hash
sha256:8c63ac4b13065bc4f0fef32693724c9b2b24297cd6a6b2a7e9aa69cb22a9344e
fork_of
null
gaps array · 15 items
[0]
asset:data:geo:GSE11691 licence not read
[1]
asset:data:geo:GSE11691 not downloaded
[2]
asset:data:geo:GSE23339 licence not read
[3]
asset:data:geo:GSE23339 not downloaded
[4]
asset:data:geo:GSE25628 licence not read
[5]
asset:data:geo:GSE25628 not downloaded
[6]
asset:data:geo:GSE7305 licence not read
[7]
asset:data:geo:GSE7305 not downloaded
[8]
asset:data:geo:GSE7846 licence not read
[9]
asset:data:geo:GSE7846 not downloaded
[10]
execution.not_run
[11]
method.reader_differs_from_extractor
[12]
review.human_critique
[13]
review.independent_reader
[14]
review.machine_critique
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
survival_analysis
definition_version
f2132e96ae6c7a4e
required_operations array · 1 item
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cox_ph
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
Through Lasso Cox regression algorithm, over-fitting risk was minimized with the glmnet package. The alteration trajectory of each variable was assessed and 10-fold cross-validated.
order_basis
analysis_only
id
assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36059959", "kind": "science-record", "revision": 4, "content_hash": "sha256:ff2fb360b23d8ee7f561b3b51b237db9f8ed111bed17effbf210b8ebf8a9a7a8", "created_at": "2026-11-01T18:15:15Z", "updated_at": "2026-11-01T22:07:27Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Integrated bioinformatics analysis uncovers characteristic genes and molecular subtyping system for endometriosis.", "doi": "10.3389/fphar.2022.932526", "pmid": "36059959", "authors": ["Zhaowei Wang", "Jia Liu", "Miaoli Li", "Lishan Lian", "Xiaojie Cui", "Tai-Wei Ng", "Maoshu Zhu"], "journal": "Frontiers in pharmacology", "year": 2022, "abstract": "Objective: Endometriosis is a chronic inflammatory estrogen-dependent disease with the growth of endometrial tissues outside the uterine cavity. Nevertheless, the etiology of endometriosis is still unclear. Integrated bioinformatics analysis was implemented to reveal the molecular mechanisms underlying this disease. Methods: A total of four gene expression datasets (GSE7305, GSE11691, GSE23339, and GSE25628) were retrieved from the GEO, which were merged into a meta-dataset, followed by the removal of batch effects via the sva package. Weighted gene co-expression network analysis (WGCNA) was implemented, and endometriosis-related genes were screened under normal and endometriosis conditions. Thereafter, characteristic genes were determined via Lasso analysis. The diagnostic performance was estimated via receiver operating characteristic curves, and epigenetic and post-transcriptional modifications were analyzed. Small molecular compounds were predicted. Unsupervised clustering analysis was conducted via non-negative matrix factorization algorithm. The enriched pathways were analyzed via gene set enrichment analysis or GSVA. Immune features were evaluated according to immune-checkpoints, HLA, receptors, chemokines, and immune cells. Results: In total, four characteristic genes (BGN, AQP1, ELMO1, and DDR2) were determined for endometriosis, all of which exhibited the favorable efficacy in diagnosing endometriosis. Their aberrant levels were modulated by epigenetic and post-transcriptional modifications. In total, 51 potential drugs were predicted against endometriosis. The characteristic genes exhibited remarkable associations with immunological function. Three subtypes were classified across endometriosis, with different mechanisms and immune features. Conclusion: Our study reveals the characteristic genes and novel molecular subtyping of endometriosis, contributing to the early diagnosis and intervention in endometriosis.", "claims": [{"id": "claim-method", "statement": "Through Lasso Cox regression algorithm, over-fitting risk was minimized with the glmnet package. The alteration trajectory of each variable was assessed and 10-fold cross-validated.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36059959", "locator": "sections[6] \"Screening characteristic genes\" paragraph 2", "quote": "Through Lasso Cox regression algorithm, over-fitting risk was minimized with the glmnet package. The alteration trajectory of each variable was assessed and 10-fold cross-validated."}], "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:36059959", "locator": "sections[29] \"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": "The AUCs (95%CI) of AQP1, BGN, DDR2, and ELMO1 were 0.96 (1.00–0.89), 0.98 (1.00–0.95), 1.00 (1.00–0.99), and 0.99 (1.00–0.98), respectively, demonstrating that each characteristic gene enabled to diagnose endometriosis accurately and sensitively (Figures 4D–G).", "kind": "quantitative", "target": {"value": 95.0, "unit": "per cent", "tolerance": null, "source": "The AUCs (95%CI) of AQP1, BGN, DDR2, and ELMO1 were 0.96 (1.00–0.89), 0.98 (1.00–0.95), 1.00 (1.00–0.99), and 0.99 (1.00–0.98), respectively, demonstrating that each characteristic gene enabled to diagnose endometriosis accurately and sensitively (Figures 4D–G)."}, "evidence": [{"asset": "source:pmid:36059959", "locator": "sections[17] \"Identification of four characteristic genes in endometriosis\" paragraph 2", "quote": "Through Lasso algorithm, four characteristic genes were determined among the shared endometriosis-related genes, containing BGN, AQP1, ELMO1, and DDR2 (Figures 4A,B)."}, {"asset": "source:pmid:36059959", "locator": "sections[17] \"Identification of four characteristic genes in endometriosis\" paragraph 2", "quote": "The AUCs (95%CI) of AQP1, BGN, DDR2, and ELMO1 were 0.96 (1.00–0.89), 0.98 (1.00–0.95), 1.00 (1.00–0.99), and 0.99 (1.00–0.98), respectively, demonstrating that each characteristic gene enabled to diagnose endometriosis accurately and sensitively (Figures 4D–G)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The AUCs (95%CI) of AQP1, BGN, DDR2, and ELMO1 were 0.96 (1.00–0.89), 0.98 (1.00–0.95), 1.00 (1.00–0.99), and 0.99 (1.00–0.98), respectively, demonstrating that each characteristic gene enabled to diagnose endometriosis accurately and sensitively (Figures 4D–G).", "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:36059959"], "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:GSE11691"], "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:GSE11691"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:36059959", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fphar.2022.932526", "sha256": "sha256:8ff347379d8218a8656fc27abf1144c411f8e1af14099b41e1a3d863d402a10c", "bytes": 35330, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fphar.2022.932526", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC9428290", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE11691", "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=GSE11691", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE11691", "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": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The datasets presented in this study can be found in online repositories. 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