
Long non-coding RNAs (lncRNAs) play key roles in diverse biological processes. Moreover, the development and progression of cancer often involves the combined actions of several lncRNAs. Here we propose a multi-step method for constructing lncRNA-lncRNA functional synergistic networks (LFSNs) through co-regulation of functional modules having three features: common coexpressed genes of lncRNA pairs, enrichment in the same functional category and close proximity within protein interaction networks. Applied to three cancers, we constructed cancer-specific LFSNs and found that they exhibit a scale free and modular architecture. In addition, cancer-associated lncRNAs tend to be hubs and are enriched within modules. Although there is little synergistic pairing of lncRNAs across cancers, lncRNA pairs involved in the same cancer hallmarks by regulating same or different biological processes. Finally, we identify prognostic biomarkers within cancer lncRNA expression datasets using modules derived from LFSNs. In summary, this proof-of-principle study indicates synergistic lncRNA pairs can be identified through integrative analysis of genome-wide expression data sets and functional information.
Male, Ovarian Neoplasms, Models, Genetic, Gene Expression Profiling, Prostatic Neoplasms, Prognosis, Gene Expression Regulation, Neoplastic, Gene Ontology, Neoplasms, Humans, Female, Gene Regulatory Networks, RNA, Long Noncoding, RNA, Messenger, Glioblastoma, Algorithms
Male, Ovarian Neoplasms, Models, Genetic, Gene Expression Profiling, Prostatic Neoplasms, Prognosis, Gene Expression Regulation, Neoplastic, Gene Ontology, Neoplasms, Humans, Female, Gene Regulatory Networks, RNA, Long Noncoding, RNA, Messenger, Glioblastoma, Algorithms
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