A novel approach to topological network analysis for the identification of metrics and signatures in non-small cell lung cancer

Non-small cell lung cancer (NSCLC), the primary histological form of lung cancer, accounts for about 25%-the highest-of all cancer deaths. As NSCLC is often undetected until symptoms appear in the late stages, it is imperative to discover more effective tumor-associated biomarkers for early diagnosis. Topological data analysis is one of the most powerful methodologies applicable to biological networks. However, current studies fail to consider the biological significance of their quantitative methods and utilize popular scoring metrics without verification, leading to low performance. To extract meaningful insights from genomic data, it is essential to understand the relationship between geometric correlations and biological function mechanisms. Through bioinformatics and network analyses, we propose a novel composite selection index, the C-Index, that best captures significant pathways and interactions in gene networks to identify biomarkers with the highest efficiency and accuracy. Furthermore, we establish a 4-gene biomarker signature that serves as a promising therapeutic target for NSCLC and personalized medicine. The C-Index and biomarkers discovered were validated with robust machine learning models. The methodology proposed for finding top metrics can be applied to effectively select biomarkers and early diagnose many diseases, revolutionizing the approach to topological network research for all cancers.

Automated summary

This article investigates the early diagnosis and treatment of non-small cell lung cancer (NSCLC) and proposes a novel composite selection index (C-Index) to identify effective biomarkers. Through topological data analysis and validation with machine learning models, they discovered a 4-gene biomarker signature that holds promise for the treatment and personalized medicine of NSCLC.