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pmid:37784081

A macrophage related signature for predicting prognosis and drug sensitivity in ovarian cancer based on integrative machine learning.

Bo Zhao · Lipeng Pei

BMC medical genomics · 2023 doi:10.1186/s12920-023-01671-z

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title
A macrophage related signature for predicting prognosis and drug sensitivity in ovarian cancer based on integrative machine learning.
doi
10.1186/s12920-023-01671-z
pmid
37784081
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[0]
Bo Zhao
[1]
Lipeng Pei
journal
BMC medical genomics
year
2023
abstract
BACKGROUND: Ovarian cancer ranks the leading cause of gynecologic cancer-related death in the United States and the fifth most common cause of cancer-related mortality among American women. Increasing evidences have highlighted the vital role of macrophages M2/M1 proportion in tumor progression, prognosis and immunotherapy. METHODS: Weighted gene co-expression network analysis (WGCNA) was performed to identify macrophages related markers. Integrative procedure including 10 machine learning algorithms were performed to develop a prognostic macrophage related signature (MRS) with TCGA, GSE14764, GSE140082 datasets. The role of MRS in tumor microenvironment (TME) and therapy response was evaluated with the data of CIBERSORT, MCPcounter, QUANTISEQ, XCELL, CIBERSORT-ABS, TIMER and EPIC, GSE91061 and IMvigor210 dataset. RESULTS: The optimal MRS developed by the combination of CoxBoost and StepCox[forward] algorithm served as an independent risk factor in ovarian cancer. Compared with stage, grade and other established prognostic signatures, the current MRS had a better performance in predicting the overall survival rate of ovarian cancer patients. Low risk score indicated a higher TME score, higher level of immune cells, higher immunophenoscore, higher tumor mutational burden, lower TIDE score and lower IC50 value in ovarian cancer. The survival prediction nomogram had a good potential for clinical application in predicting the 1-, 3-, and 5-year overall survival rate of ovarian cancer patients. CONCLUSION: All in all, the current study constructed a powerful prognostic MRS for ovarian cancer patients using 10 machine learning algorithms. This MRS could predict the prognosis and drug sensitivity in ovarian cancer.
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Weighted gene co-expression network analysis (WGCNA) was performed to identify macrophages related markers.
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The analyzed data sets generated during the study were sourced from the TCGA database (https://portal.gdc.cancer.gov/repository) and GEO database (https://www.ncbi.nlm.nih.gov/geo).
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The optimal prognostic macrophages-related signature combined CoxBoost and StepCox[forward] and achieved the highest average C-index of 0.63.
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sections[14] "Integrative machine learning algorithms constructed a prognostic MRS" paragraph 2
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Finally, the model constructed by the combination of CoxBoost and StepCox[forward] was suggested as the optimal model with the highest average C-index of 0.63 (Fig. 3B).
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[79]
GSM368740
sample_count
80
group_sizes
null
group_sizes_basis
null
platform
96
taxon
Homo sapiens
title
A Prognostic Gene Expression Index in Ovarian Cancer
resolution_checked_at
2026-11-01T17:30:42Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
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[0]
asset:data:geo:GSE140082 not downloaded
[1]
asset:data:geo:GSE140082 licence not read
[2]
asset:data:geo:GSE14764 not downloaded
[3]
asset:data:geo:GSE14764 licence not read
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partial
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method-1
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survival_analysis
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cox_proportional_hazards
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Survival analysis
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cox_ph
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parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
1
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verbatim
quote
Weighted gene co-expression network analysis (WGCNA) was performed to identify macrophages related markers.
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id
method-2
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group_comparison
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student_t_test
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Group comparison
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missing_operations array · 1 item
[0]
student_t
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parameters object · 0 fields
data_shapes array · 1 item
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two_or_more_groups_continuous
evidence object · 3 fields
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quote
student T test
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group_comparison
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label
Group comparison
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missing_operations array · 1 item
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two_or_more_groups_continuous
evidence object · 3 fields
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quote
Wilcoxon
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method-4
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survival_analysis
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Survival analysis
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survival_km
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
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0.8
band
high
quote
Kaplan-Meier
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method-5
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survival_analysis
specific
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label
Survival analysis
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[0]
logrank_test
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time_to_event_with_censoring
evidence object · 3 fields
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method.reader_differs_from_extractor
capability object · 3 fields
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capability:computational_analysis
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Computational analysis platform
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[8]
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candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
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complete
tier
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cox_ph
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards.
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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
reachable
true
accessions array · 2 items
[0]
GSE14764
[1]
GSE140082
resolved_accessions array · 2 items
[0]
GSE14764
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GSE140082
statements array · 1 item
[0]
The analyzed data sets generated during the study were sourced from the TCGA database (https://portal.gdc.cancer.gov/repository) and GEO database (https://www.ncbi.nlm.nih.gov/geo).
basis
The paper names GSE14764, GSE140082 in GEO database 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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cox_ph
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source:pmid:37784081
[1]
data:geo:GSE140082
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run_analysis
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data:geo:GSE140082
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review object · 5 fields
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partial
machine_critique object · 5 fields
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extraction_review
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MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T18:54:55Z
independence
single_reader
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method
verbatim
availability
verbatim
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9599
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128
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[0] object · 4 fields
id
extraction
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complete
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MiniMax-M3.1-Flash
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minimax
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review.independent_reader
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review.human_critique
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absent
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not_run
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null
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execution.not_run
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pmid:37784081
type
paper
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pmid:37784081
[1] object · 3 fields
id
source:pmid:37784081
type
manuscript
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PMID 37784081 full text
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data:geo:GSE140082
type
dataset
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GEO GSE140082
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activity-reading-sci-2026-11-01
type
classification
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pmid:37784081
type
paper
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pmid:37784081
[1] object · 3 fields
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source:pmid:37784081
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manuscript
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PMID 37784081 full text
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id
data:geo:GSE140082
type
dataset
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GEO GSE140082
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agent:corpus-assay-engine
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id
activity-read-37784081
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extraction
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source:pmid:37784081
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agent:minimax-reader
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activity-resolve-GSE140082
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accession_resolution
used array · 1 item
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data:geo:GSE140082
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agent:corpus-assay-engine
agents array · 2 items
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agent:corpus-assay-engine
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software
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Corpus assay engine
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agent:minimax-reader
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MiniMax literature reader
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dsl_catalogue_fingerprint
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capability_table_fingerprint
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lineage object · 4 fields
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evidence array · 1 item
[0]
, QUANTISEQ, XCELL, CIBERSORT-ABS, TIMER and EPIC, GSE91061 and IMvigor210 dataset. RESULTS: T
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dsl_catalogue
f2132e96ae6c7a4e
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Weighted gene co-expression network analysis (WGCNA) was performed to identify macrophages related markers.
order_basis
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37784081", "kind": "science-record", "revision": 3, "content_hash": "sha256:81a47938e756851455beb5c5408b49188230cdd326ee23fe5f9feff589fc1626", "created_at": "2026-11-01T19:02:38Z", "updated_at": "2026-11-01T22:10:23Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A macrophage related signature for predicting prognosis and drug sensitivity in ovarian cancer based on integrative machine learning.", "doi": "10.1186/s12920-023-01671-z", "pmid": "37784081", "authors": ["Bo Zhao", "Lipeng Pei"], "journal": "BMC medical genomics", "year": 2023, "abstract": "BACKGROUND: Ovarian cancer ranks the leading cause of gynecologic cancer-related death in the United States and the fifth most common cause of cancer-related mortality among American women. Increasing evidences have highlighted the vital role of macrophages M2/M1 proportion in tumor progression, prognosis and immunotherapy.\nMETHODS: Weighted gene co-expression network analysis (WGCNA) was performed to identify macrophages related markers. Integrative procedure including 10 machine learning algorithms were performed to develop a prognostic macrophage related signature (MRS) with TCGA, GSE14764, GSE140082 datasets. The role of MRS in tumor microenvironment (TME) and therapy response was evaluated with the data of CIBERSORT, MCPcounter, QUANTISEQ, XCELL, CIBERSORT-ABS, TIMER and EPIC, GSE91061 and IMvigor210 dataset.\nRESULTS: The optimal MRS developed by the combination of CoxBoost and StepCox[forward] algorithm served as an independent risk factor in ovarian cancer. Compared with stage, grade and other established prognostic signatures, the current MRS had a better performance in predicting the overall survival rate of ovarian cancer patients. Low risk score indicated a higher TME score, higher level of immune cells, higher immunophenoscore, higher tumor mutational burden, lower TIDE score and lower IC50 value in ovarian cancer. The survival prediction nomogram had a good potential for clinical application in predicting the 1-, 3-, and 5-year overall survival rate of ovarian cancer patients.\nCONCLUSION: All in all, the current study constructed a powerful prognostic MRS for ovarian cancer patients using 10 machine learning algorithms. This MRS could predict the prognosis and drug sensitivity in ovarian cancer.", "claims": [{"id": "claim-method", "statement": "Weighted gene co-expression network analysis (WGCNA) was performed to identify macrophages related markers.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37784081", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Weighted gene co-expression network analysis (WGCNA) was performed to identify macrophages related markers."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The analyzed data sets generated during the study were sourced from the TCGA database (https://portal.gdc.cancer.gov/repository) and GEO database (https://www.ncbi.nlm.nih.gov/geo).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37784081", "locator": "sections[30] \"notes\" paragraph 1", "quote": "The analyzed data sets generated during the study were sourced from the TCGA database (https://portal.gdc.cancer.gov/repository) and GEO database (https://www.ncbi.nlm.nih.gov/geo)."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The optimal prognostic macrophages-related signature combined CoxBoost and StepCox[forward] and achieved the highest average C-index of 0.63.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37784081", "locator": "sections[14] \"Integrative machine learning algorithms constructed a prognostic MRS\" paragraph 2", "quote": "Finally, the model constructed by the combination of CoxBoost and StepCox[forward] was suggested as the optimal model with the highest average C-index of 0.63 (Fig. 3B)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The optimal prognostic macrophages-related signature combined CoxBoost and StepCox[forward] and achieved the highest average C-index of 0.63.", "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:37784081"], "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:GSE140082"], "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:GSE140082"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37784081", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1186/s12920-023-01671-z", "sha256": "sha256:6aae36ef6e7cf26067add4c129c4eea5179e4b2679ebe6234022c9220db51120", "bytes": 32907, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1186/s12920-023-01671-z", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC10544447", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE140082", "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=GSE140082", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE140082", "version": null, "note": "The analyzed data sets generated during the study were sourced from the TCGA database 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