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Biology subjects

Ewing, R.

Publications and source records attributed to Ewing, R..

2 recordsLinked to original sources

iOmicsPASS: a novel method for integration of multi-omics data over biological networks and discovery of predictive subnetworks

We developed iOmicsPASS, an intuitive method for network-based multi-omics data integration and detection of biological subnetworks for phenotype prediction. The method converts abundance measurements into co-expression scores of biological networks and uses a powerful phenotype prediction method adapted for network-wise analysis. Simulation studies show that the proposed data integration approach considerably improves the quality of predictions. We illustrate iOmicsPASS through the integration of quantitative multi-omics data using transcription factor regulatory network and protein-protein interaction network for cancer subtype prediction. Our analysis of breast cancer data identifies network signatures surrounding established markers of molecular subtypes. The analysis of colorectal cancer data highlights a protein interactome surrounding key proto-oncogenes as predictive features of subtypes, rendering them more biologically interpretable than the approaches integrating data without a priori relational information. However, the results indicate that current molecular subtyping is overly dependent on transcriptomic data and crude integrative analysis fails to account for molecular heterogeneity in other -omics data. The analysis also suggest that tumor subtypes are not mutually exclusive and future subtyping should therefore consider multiplicity in assignments.\n\nAvailability: https://github.com/cssblab/iOmicsPASS

systems biology

The PTPRT pseudo-phosphatase domain is a denitrase

Protein tyrosine nitration occurs under both physiological and pathological conditions1. However, enzymes that remove this protein modification have not yet been identified. Here we report that the pseudo-phosphatase domain of protein tyrosine receptor T (PTPRT) is a denitrase that removes nitro-groups from tyrosine residues in paxillin. PTPRT normally functions as a tumor suppressor and is frequently mutated in a variety of human cancers including colorectal cancer2,3. We demonstrate that some of the tumor-derived mutations located in the pseudophosphatase domain impair the denitrase activity. Moreover, PTPRT mutant mice that inactivate the denitrase activity are susceptible to carcinogen-induced colon tumor formation. This study uncovers a novel enzymatic activity that is involved in tumor suppression.

cancer biology