Comparative analyses of gene networks mediating cancer metastatic potentials across lineage types

• Published in: Briefings in bioinformatics Vol. 25; no. 4
• Main Authors: Wang, Sheng, Stroup, Emily K, Wang, Ting-You, Yang, Rendong, Ji, Zhe
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 23.05.2024; Oxford Publishing Limited (England)
• Subjects: Cancer; Cell cycle; Cell Lineage - genetics; Comparative analysis; Correlation coefficient; Correlation coefficients; Gene expression; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Gene Regulatory Networks; Humans; In vivo methods and tests; Metastases; Metastasis; Neoplasm Metastasis; Neoplasms - genetics; Neoplasms - metabolism; Neoplasms - pathology; Networks; Problem Solving Protocol; Protein Interaction Maps - genetics; Proteins; Regression models; Transcriptome; Transcriptomics; lineage types; drug response; gene network; cancer metastasis
• ISSN: 1467-5463; 1477-4054; 1477-4054
• DOI: 10.1093/bib/bbae357

Abstract Studies have identified genes and molecular pathways regulating cancer metastasis. However, it remains largely unknown whether metastatic potentials of cancer cells from different lineage types are driven by the same or different gene networks. Here, we aim to address this question through integrative analyses of 493 human cancer cells’ transcriptomic profiles and their metastatic potentials in vivo. Using an unsupervised approach and considering both gene coexpression and protein–protein interaction networks, we identify different gene networks associated with various biological pathways (i.e. inflammation, cell cycle, and RNA translation), the expression of which are correlated with metastatic potentials across subsets of lineage types. By developing a regularized random forest regression model, we show that the combination of the gene module features expressed in the native cancer cells can predict their metastatic potentials with an overall Pearson correlation coefficient of 0.90. By analyzing transcriptomic profile data from cancer patients, we show that these networks are conserved in vivo and contribute to cancer aggressiveness. The intrinsic expression levels of these networks are correlated with drug sensitivity. Altogether, our study provides novel comparative insights into cancer cells’ intrinsic gene networks mediating metastatic potentials across different lineage types, and our results can potentially be useful for designing personalized treatments for metastatic cancers.