Independent component analysis uncovers the landscape of the bladder tumor transcriptome and reveals insights into luminal and basal subtypes

Biton, Anne; Bernard-Pierrot, Isabelle; Lou, Yinjun; Krucker, Clémentine; Chapeaublanc, Elodie; Rubio Pérez, Carlota, 1990-; López Bigas, Núria; Kamoun, Aurélie; Neuzillet, Yann; Gestraud, Pierre; Grieco, Luca; Rebouissou, Sandra; deReyniès, Aurélien; Benhamou, Simone; Lebret, Thierry; Southgate, Jennifer; Barillot, Emmanuel; Allory, Yves; Zinovyev, Andrei; Radvanyi, François

doi:http://dx.doi.org/10.1016/j.celrep.2014.10.035

Independent component analysis uncovers the landscape of the bladder tumor transcriptome and reveals insights into luminal and basal subtypes

Citation

Biton A, Bernard-Pierrot I, Lou Y, Krucker C, Chapeaublanc E, Rubio-Pérez C et al. Independent component analysis uncovers the landscape of the bladder tumor transcriptome and reveals insights into luminal and basal subtypes. Cell Reports. 2014;9(4):1235-45. DOI: 10.1016/j.celrep.2014.10.035

Abstract

Extracting relevant information from large-scale data offers unprecedented opportunities in cancerology. We applied independent component analysis (ICA) to bladder cancer transcriptome data sets and interpreted the components using gene enrichment analysis and tumor-associated molecular, clinicopathological, and processing information. We identified components associated with biological processes of tumor cells or the tumor microenvironment, and other components revealed technical biases. Applying ICA to nine cancer types identified cancer-shared and bladder-cancer-specific components. We characterized the luminal and basal-like subtypes of muscle-invasive bladder cancers according to the components identified. The study of the urothelial differentiation component, specific to the luminal subtypes, showed that a molecular urothelial differentiation program was maintained even in those luminal tumors that had lost morphological differentiation. Study of the genomic alterations associated with this component coupled with functional studies revealed a protumorigenic role for PPARG in luminal tumors. Our results support the inclusion of ICA in the exploitation of multiscale data sets.