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pmid:37351348

Vasculogenic mimicry score identifies the prognosis and immune landscape of lung adenocarcinoma.

Weichang Yang · Zhouhua Li · Wenjun Wang · Juan Wu · Jinbo Li · Xiaotian Huang · Xinyi Zhang · Xiaoqun Ye

Frontiers in genetics · 2023 doi:10.3389/fgene.2023.1206141

Paper

complete

Experiment

partial

Data

partial

Analysis

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Execution

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title
Vasculogenic mimicry score identifies the prognosis and immune landscape of lung adenocarcinoma.
doi
10.3389/fgene.2023.1206141
pmid
37351348
authors array · 8 items
[0]
Weichang Yang
[1]
Zhouhua Li
[2]
Wenjun Wang
[3]
Juan Wu
[4]
Jinbo Li
[5]
Xiaotian Huang
[6]
Xinyi Zhang
[7]
Xiaoqun Ye
journal
Frontiers in genetics
year
2023
abstract
Background: Lung cancer has a high incidence and mortality rate worldwide. Vasculogenic mimicry (VM) is a specific modality of tumor angiogenesis that could potentially be a new target for tumor therapy. The purpose of this study was to explore the role of VM-related genes in assessing the prognosis and immune landscape of lung cancer. Methods: VM-related genes were obtained from previous studies, and the expression data and clinical data of lung adenocarcinoma (LUAD) patients were obtained from the TCGA database and GEO database. We performed enrichment analysis of 24 VM-related genes and screened hub genes by constructing a protein-protein interaction network and using Cytoscape software. Subsequently, we developed the VM score based on univariate Cox regression analysis and Lasso analysis and validated the VM score on the GSE72094 dataset. In addition, we constructed a nomogram based on the VM score in the TCGA cohort. Finally, we explored the correlation between the VM score and the tumor microenvironment, immune cell infiltration, immune checkpoints, and drug sensitivity. Results: Enrichment analysis revealed that VM-related genes were associated with the HIF signaling pathway and angiogenic pathway. We developed a VM score based on 3 genes (EPHA2, LAMC2 and LOXL2) in LUAD patients. Kaplan-Meier analysis showed that the VM score was associated with poor prognosis in LUAD patients. The receiver operating characteristic curve suggested that the VM score and nomogram are valid predictors for the overall survival of LUAD patients. The VM score was significantly correlated with immune cell infiltration, such as naïve B cells, neutrophils, and eosinophils, and there was a difference in the TME between the high VM score group and the low VM score group. LUAD patients in the high VM score group were more sensitive to antitumor drugs. Conclusion: In summary, the VM score developed in this study is a valuable indicator for evaluating the prognosis and immune landscape of LUAD patients. VM may be a potential target for antitumor therapy in lung cancer.
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The Wilcoxon test, Spearman correlation analysis and survival analysis were used in this study.
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The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
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We developed a VM score based on 3 genes (EPHA2, LAMC2 and LOXL2) in LUAD patients.
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We developed a VM score based on 3 genes (EPHA2, LAMC2 and LOXL2) in LUAD patients.
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null
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15048
taxon
Homo sapiens
title
KRAS mutation-associated gene expression, p53 and STK11 mutations, proliferation and immune surveillance in lung adenocarcinoma
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2026-11-01T15:39:55Z
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identifier_resolution_only_no_download_no_licence_read
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tier
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owned
basis
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tier
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[0]
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GSE36471
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[0]
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
basis
The paper names GSE72094, GSE36471 in GEO database and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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group_comparison_wilcoxon
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null
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[0]
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partial
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minimax
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minimax
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independence
single_reader
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extraction
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paper
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source:pmid:37351348
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data:geo:GSE36471
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GEO GSE36471
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classification
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paper
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source:pmid:37351348
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GEO GSE36471
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agent:corpus-assay-engine
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f2132e96ae6c7a4e
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The Wilcoxon test, Spearman correlation analysis and survival analysis were used in this study.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37351348", "kind": "science-record", "revision": 4, "content_hash": "sha256:8c7bdcea2f3312a8ab2c04e13c1915a036c2633edb22e8b26f66247ed197eb1d", "created_at": "2026-11-01T19:02:05Z", "updated_at": "2026-11-01T22:52:10Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Vasculogenic mimicry score identifies the prognosis and immune landscape of lung adenocarcinoma.", "doi": "10.3389/fgene.2023.1206141", "pmid": "37351348", "authors": ["Weichang Yang", "Zhouhua Li", "Wenjun Wang", "Juan Wu", "Jinbo Li", "Xiaotian Huang", "Xinyi Zhang", "Xiaoqun Ye"], "journal": "Frontiers in genetics", "year": 2023, "abstract": "Background: Lung cancer has a high incidence and mortality rate worldwide. Vasculogenic mimicry (VM) is a specific modality of tumor angiogenesis that could potentially be a new target for tumor therapy. The purpose of this study was to explore the role of VM-related genes in assessing the prognosis and immune landscape of lung cancer. Methods: VM-related genes were obtained from previous studies, and the expression data and clinical data of lung adenocarcinoma (LUAD) patients were obtained from the TCGA database and GEO database. We performed enrichment analysis of 24 VM-related genes and screened hub genes by constructing a protein-protein interaction network and using Cytoscape software. Subsequently, we developed the VM score based on univariate Cox regression analysis and Lasso analysis and validated the VM score on the GSE72094 dataset. In addition, we constructed a nomogram based on the VM score in the TCGA cohort. Finally, we explored the correlation between the VM score and the tumor microenvironment, immune cell infiltration, immune checkpoints, and drug sensitivity. Results: Enrichment analysis revealed that VM-related genes were associated with the HIF signaling pathway and angiogenic pathway. We developed a VM score based on 3 genes (EPHA2, LAMC2 and LOXL2) in LUAD patients. Kaplan-Meier analysis showed that the VM score was associated with poor prognosis in LUAD patients. The receiver operating characteristic curve suggested that the VM score and nomogram are valid predictors for the overall survival of LUAD patients. The VM score was significantly correlated with immune cell infiltration, such as naïve B cells, neutrophils, and eosinophils, and there was a difference in the TME between the high VM score group and the low VM score group. LUAD patients in the high VM score group were more sensitive to antitumor drugs. Conclusion: In summary, the VM score developed in this study is a valuable indicator for evaluating the prognosis and immune landscape of LUAD patients. 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