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pmid:37781711

Comprehensive analysis of Cuproplasia and immune microenvironment in lung adenocarcinoma.

Junjie Kuang · Zemao Zheng · Wen Ma · Shaohui Zeng · Dehua Wu · Xie Weng · Yuming Chen

Frontiers in pharmacology · 2023 doi:10.3389/fphar.2023.1240736

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complete

Experiment

complete

Data

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Analysis

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Execution

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pmid:37781711
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title
Comprehensive analysis of Cuproplasia and immune microenvironment in lung adenocarcinoma.
doi
10.3389/fphar.2023.1240736
pmid
37781711
authors array · 7 items
[0]
Junjie Kuang
[1]
Zemao Zheng
[2]
Wen Ma
[3]
Shaohui Zeng
[4]
Dehua Wu
[5]
Xie Weng
[6]
Yuming Chen
journal
Frontiers in pharmacology
year
2023
abstract
Background: Trace elements such as copper are essential for human health. Recently the journal Nat Rev Cancer has put forward the concept of Cuproplasia, a way of promoting tumor growth through reliance on copper. We attempted to conduct a comprehensive analysis of Cuproplasia-related genes in lung adenocarcinoma (LUAD) to explore the mechanism of action of Cuproplasia-related genes in LUAD. Method: Transcriptome data and clinical information of LUAD were obtained from TCGA-LUAD and GSE31210, and prognostic models of Cuproplasia-related genes were constructed and verified by regression analysis of GSVA, WGCNA, univariate COX and lasso. The signal pathways affected by Cuproplasia-related genes were analyzed by GO, KEGG and hallmarK pathway enrichment methods. Five immunocell infiltration algorithms and IMVIGOR210 data were used to analyze immune cell content and immunotherapy outcomes in the high-low risk group. Results: In the results of WGCNA, BROWN and TURQUOISE were identified as modules closely related to Cuproplasia score. In the end, lasso regression analysis established a Cuproplasia-related signature (CRS) based on 24 genes, and the prognosis of high-risk populations was worse in TCGA-LUAD and GSE31210 datasets. The enrichment analysis showed that copper proliferation was mainly through chromosome, cell cycle, dna replication, g2m checkpoint and other pathways. Immunoinfiltration analysis showed that there were differences in the content of macrophages among the four algorithms. And IMVIGOR210 found that the lower the score, the more effective the immunotherapy was. Conclusion: The Cuproplasia related gene can be used to predict the prognosis and immunotherapy outcome of LUAD patients, and may exert its effect by affecting chromosome-related pathways and macrophages.
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Univariate Cox regression analysis was performed for differential gene expression and overall survival between tumor and normal tissues to screen out prognostic copper proliferating genes.
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Univariate Cox regression analysis was performed for differential gene expression and overall survival between tumor and normal tissues to screen out prognostic copper proliferating genes.
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Lasso regression analysis established a 24-gene Cuproplasia-related signature, and prognosis was worse in the high-risk populations in the TCGA-LUAD and GSE31210 datasets.
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In the end, lasso regression analysis established a Cuproplasia-related signature (CRS) based on 24 genes, and the prognosis of high-risk populations was worse in TCGA-LUAD and GSE31210 datasets.
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Lasso regression analysis established a 24-gene Cuproplasia-related signature, and prognosis was worse in the high-risk populations in the TCGA-LUAD and GSE31210 datasets.
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[1] 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]
Univariate Cox regression analysis was performed for differential gene expression and overall survival between tumor and normal tissues to screen out prognostic copper proliferating genes.
order_basis
consumes_earlier_output
id
assay:2
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37781711", "kind": "science-record", "revision": 3, "content_hash": "sha256:24b4851b63c5bae69b074bcc04661e23bbabec5eb8724332e8644cb5df17a1fa", "created_at": "2026-11-01T19:02:37Z", "updated_at": "2026-11-01T22:10:23Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Comprehensive analysis of Cuproplasia and immune microenvironment in lung adenocarcinoma.", "doi": "10.3389/fphar.2023.1240736", "pmid": "37781711", "authors": ["Junjie Kuang", "Zemao Zheng", "Wen Ma", "Shaohui Zeng", "Dehua Wu", "Xie Weng", "Yuming Chen"], "journal": "Frontiers in pharmacology", "year": 2023, "abstract": "Background: Trace elements such as copper are essential for human health. Recently the journal Nat Rev Cancer has put forward the concept of Cuproplasia, a way of promoting tumor growth through reliance on copper. We attempted to conduct a comprehensive analysis of Cuproplasia-related genes in lung adenocarcinoma (LUAD) to explore the mechanism of action of Cuproplasia-related genes in LUAD. Method: Transcriptome data and clinical information of LUAD were obtained from TCGA-LUAD and GSE31210, and prognostic models of Cuproplasia-related genes were constructed and verified by regression analysis of GSVA, WGCNA, univariate COX and lasso. The signal pathways affected by Cuproplasia-related genes were analyzed by GO, KEGG and hallmarK pathway enrichment methods. Five immunocell infiltration algorithms and IMVIGOR210 data were used to analyze immune cell content and immunotherapy outcomes in the high-low risk group. Results: In the results of WGCNA, BROWN and TURQUOISE were identified as modules closely related to Cuproplasia score. In the end, lasso regression analysis established a Cuproplasia-related signature (CRS) based on 24 genes, and the prognosis of high-risk populations was worse in TCGA-LUAD and GSE31210 datasets. The enrichment analysis showed that copper proliferation was mainly through chromosome, cell cycle, dna replication, g2m checkpoint and other pathways. Immunoinfiltration analysis showed that there were differences in the content of macrophages among the four algorithms. And IMVIGOR210 found that the lower the score, the more effective the immunotherapy was. Conclusion: The Cuproplasia related gene can be used to predict the prognosis and immunotherapy outcome of LUAD patients, and may exert its effect by affecting chromosome-related pathways and macrophages.", "claims": [{"id": "claim-method", "statement": "Univariate Cox regression analysis was performed for differential gene expression and overall survival between tumor and normal tissues to screen out prognostic copper proliferating genes.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37781711", "locator": "sections[7] \"Screening of prognostic related copper proliferating genes\" paragraph 2", "quote": "Univariate Cox regression analysis was performed for differential gene expression and overall survival between tumor and normal tissues to screen out prognostic copper proliferating genes."}], "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:37781711", "locator": "sections[36] \"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": "Lasso regression analysis established a 24-gene Cuproplasia-related signature, and prognosis was worse in the high-risk populations in the TCGA-LUAD and GSE31210 datasets.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37781711", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "In the end, lasso regression analysis established a Cuproplasia-related signature (CRS) based on 24 genes, and the prognosis of high-risk populations was worse in TCGA-LUAD and GSE31210 datasets."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Lasso regression analysis established a 24-gene Cuproplasia-related signature, and prognosis was worse in the high-risk populations in the TCGA-LUAD and GSE31210 datasets.", "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:37781711"], "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:GSE31210"], "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:GSE31210"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37781711", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fphar.2023.1240736", "sha256": "sha256:099a76f4c7e8f84ebc87bc819e21faa8ca164af573f9b6ffa3ac209f414eac45", "bytes": 54357, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fphar.2023.1240736", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC10540310", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE31210", "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=GSE31210", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE31210", "version": null, "note": "The datasets presented in this study can be found in online repositories. 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