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pmid:35398839

A novel classification method for NSCLC based on the background interaction network and the edge-perturbation matrix.

Yuan Tian · Caiqing Zhang · Wanru Ma · Alan Huang · Mei Tian · Junyan Zhao · Qi Dang · Yuping Sun

Aging · 2022 doi:10.18632/aging.204004

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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pmid:35398839
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science-record
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title
A novel classification method for NSCLC based on the background interaction network and the edge-perturbation matrix.
doi
10.18632/aging.204004
pmid
35398839
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Yuan Tian
[1]
Caiqing Zhang
[2]
Wanru Ma
[3]
Alan Huang
[4]
Mei Tian
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Junyan Zhao
[6]
Qi Dang
[7]
Yuping Sun
journal
Aging
year
2022
abstract
The biological functional network of tumor tissues is relatively stable for a period of time and under different conditions, so the impact of tumor heterogeneity is effectively avoided. Based on edge perturbation, functional gene interaction networks were used to reveal the pathological environment of patients with non-small cell carcinoma at the individual level, and to identify cancer subtypes with the same or similar status, and then a multi-dimensional and multi-omics comprehensive analysis was put into practice. Two edge perturbation subtypes were identified through the construction of the background interaction network and the edge-perturbation matrix (EPM). Further analyses revealed clear differences between those two clusters in terms of prognostic survival, stemness indices, immune cell infiltration, immune checkpoint molecular expression, copy number alterations, mutation load, homologous recombination defects (HRD), neoantigen load, and chromosomal instability. Additionally, a risk prediction model based on TCGA for lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC) was successfully constructed and validated using the independent data set (GSE50081).
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According to the Kruskal-Wallis test, the difference of the edge disturbance matrix between the normal and the cancer sample was calculated, and the top 30,000 different edges would be selected according to the level of significant difference
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sections[5] "Construction of the background interaction network and edge-perturbation matrix" paragraph 10
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According to the Kruskal-Wallis test, the difference of the edge disturbance matrix between the normal and the cancer sample was calculated, and the top 30,000 different edges would be selected according to the level of significant difference
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Two edge perturbation subtypes were identified through the construction of the background interaction network and the edge-perturbation matrix (EPM).
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Two edge perturbation subtypes were identified through the construction of the background interaction network and the edge-perturbation matrix (EPM).
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Complete file
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Based on edge perturbation, functional gene interaction networks were used to reveal the pathological environment of patients with non-small cell carcinoma at the individual level, and to identify cancer subtypes with the same or similar status, and then a multi-dimensional and multi-omics comprehensive analysis was put into practice. Two edge perturbation subtypes were identified through the construction of the background interaction network and the edge-perturbation matrix (EPM). Further analyses revealed clear differences between those two clusters in terms of prognostic survival, stemness indices, immune cell infiltration, immune checkpoint molecular expression, copy number alterations, mutation load, homologous recombination defects (HRD), neoantigen load, and chromosomal instability. 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