Abstract
Toxicogenomics studies typically reveal a group of genes relevant to the pathophysiology of drug-induced organ injury. In recent years, network-based methods have become an attractive analytical approach as they can capture not only the global changes of regulatory gene networks but also the relationships between their components. Among them, a causal reasoning approach additionally depicts the mechanisms of regulation that connect upstream regulators in signaling networks towards their downstream gene targets.
In this work, we applied CARNIVAL, a causal network contextualisation tool, to infer upstream regulatory signaling networks based on gene expression microarray data from the TG-GATEs database. We focussed on six compounds that induce observable histopathologies linked to drug-induced liver injury (DILI) from repeated dosing experiments in rats. We compared responses in vitro and in vivo to identify potential cross-platform concordances in rats as well as network preservations between rat and human. Our results showed similarities of enriched pathways and network motifs between compounds. These pathways and motifs induce the same pathology in rats but not in humans. In particular, the causal interactions “LCK activates SOCS3, which in turn inhibits TFDP1” was commonly identified as a regulatory path among the fibrosis-inducing compounds. This potential pathology-inducing regulation illustrates the value of our approach to generate hypotheses that can be further validated experimentally.
Competing Interest Statement
The authors have declared no competing interest.
