| Literature DB >> 33578936 |
Alessandro Palma1, Marta Iannuccelli1, Ilaria Rozzo1, Luana Licata1, Livia Perfetto1,2, Giorgia Massacci1, Luisa Castagnoli1, Gianni Cesareni1, Francesca Sacco1.
Abstract
High throughput technologies such as deep sequencing and proteomics are increasingly becoming mainstream in clinical practice and support diagnosis and patient stratification. Developing computational models that recapitulate cell physiology and its perturbations in disease is a required step to help with the interpretation of results of high content experiments and to devise personalized treatments. As complete cell-models are difficult to achieve, given limited experimental information and insurmountable computational problems, approximate approaches should be considered. We present here a general approach to modeling complex diseases by embedding patient-specific genomics data into actionable logic models that take into account prior knowledge. We apply the strategy to acute myeloid leukemia (AML) and assemble a network of logical relationships linking most of the genes that are found frequently mutated in AML patients. We derive Boolean models from this network and we show that by priming the model with genomic data we can infer relevant patient-specific clinical features. Here we propose that the integration of literature-derived causal networks with patient-specific data should be explored to help bedside decisions.Entities:
Keywords: Boolean networks; acute myeloid leukemia; logic modelling; signaling
Year: 2021 PMID: 33578936 PMCID: PMC7916657 DOI: 10.3390/jpm11020117
Source DB: PubMed Journal: J Pers Med ISSN: 2075-4426