Skip to content
2000
Volume 18, Issue 6
  • ISSN: 1574-8936
  • E-ISSN: 2212-392X

Abstract

Introduction: Lung cancer is the leading cancer in terms of morbidity and mortality rate. Its prevalence has been steadily increasing over the world in recent years. An integrated study is unavoidable to analyse the cascading interrelationships between molecular cell components at multiple levels resulting in hidden biological events in cancer. Methods: Multiplex network modeling is a unique methodology that could be used as an integrative method for dealing with diverse interactions. Here, we have employed a multiplex framework to model the lung adenocarcinoma (LUAD) network by incorporating co-expression correlations, methylation relations, and protein physical binding interactions as network layers. Hub nodes identified from the multiplex network utilizing centrality measures, including degree, eigenvector, and random walk with a random jump technique, are considered as biomarker genes. These stage-wise biomarker genes identified for LUAD are investigated using GO enrichment analysis, pathway analysis, and literature evidence to determine their significance in tumor progression. Results: The study has identified a set of stage-specific biomarkers in LUAD. The 31 genes identified from the results of multiple centrality analysis can be targeted as novel diagnostic biomarkers in LUAD. Multiple signaling pathways identified here may be considered as potential targets of interest. Conclusion: Based on the analysis results, patients may be identified by their stage of cancer progression, which can aid in treatment decision-making.

Loading

Article metrics loading...

/content/journals/cbio/10.2174/1574893618666230228112411
2023-07-01
2025-04-22
Loading full text...

Full text loading...

/content/journals/cbio/10.2174/1574893618666230228112411
Loading
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test