| Summary: | Identification of molecular-based signatures is one of the critical steps toward finding therapeutic targets in cancer. In this paper, we propose methods to discover prognostic gene signatures under a causal structure learning framework across the whole genome. The causal structures are represented by directed acyclic graphs (DAGs), wherein we construct gene-specific network modules that constitute a gene and its corresponding regulators. The modules are then subsequently used to correlate with survival times, thus, allowing for a network-oriented approach to gene selection to adjust for potential confounders, as opposed to univariate (gene-by-gene) approaches. Our methods are motivated by and applied to a clear cell renal cell carcinoma (ccRCC) study from The Cancer Genome Atlas (TCGA) where we find several prognostic genes associated with cancer progression - some of which are novel while others confirm existing findings.
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