Protein-protein interaction and gene regulatory networks are likely to be locked in a state corresponding to a disease by the behavior of one or more bistable circuits exhibiting switch-like behavior. Sets of genes could be over-expressed or repressed when anomalies due to disease appear, and the circuits responsible for this over- or under-expression might persist for as long as the disease state continues. This paper shows how a large-scale analysis of network bistability for various human cancers can identify genes that can potentially serve as drug targets or diagnosis biomarkers. © 2010 Shiraishi et al.
CITATION STYLE
Shiraishi, T., Matsuyama, S., & Kitano, H. (2010). Large-scale analysis of network bistability for human cancers. PLoS Computational Biology, 6(7), 26. https://doi.org/10.1371/journal.pcbi.1000851
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