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Chahley, N.

Publications and source records attributed to Chahley, N..

2 recordsLinked to original sources

Higher-Order Biomarkers Through Network Motif Mining: A COVID-19 Case Study

We introduce a novel approach for analyzing expression data by integrating patient-level expression profiles with a Protein-Protein interaction network from the STRING database. Our pipeline leverages motif mining to identify recurring sets (motifs) of interacting biomolecules characterized by specific expression patterns, providing deeper insights into underlying biological processes. We applied our method to a publicly available dataset of plasma protein measurements from patients with mild/moderate COVID-19 and compared the motif features to those found by conventional differential expression analysis. Motif features demonstrated better performance in classification models and hierarchical clustering. Of note, they were able to resolve interpatient variability during clustering, while traditional features failed to do so. Interestingly, these discriminatory performances were achieved using a smaller and largely different set of proteins. Motif mining is a highly flexible method with capacity to integrate multiple modes of data and presents an exciting line of analysis for biomarker discovery as well as general biology.

bioinformatics↗

Beyond Conventional Models: Recreating the Initiation, Evolution, and Genome of GBM

BackgroundImagining ways to prevent or treat glioblastoma (GBM) have been hindered by a lack of understanding of its pathogenesis. Although PDGF-AA overexpression may be an early event, critical details of the core biology are lacking. Existing PDGF-driven models replicate its microscopic appearance but not the genomic architecture characteristic of the human disease. Here we report a new model of GBM that overcomes this barrier to authenticity. MethodsUsing a method developed to study neural stem cells, we investigated the effects of PDGF-AA on subventricular zone (SVZ) cells, the putative cell of origin of GBM. We micro-dissected SVZ tissue from p53-null and wild-type adult mice, established primary cultures in media supplemented with PDGF-AA, and assessed cell viability, proliferation, genome stability, and tumour forming potential. ResultsCounterintuitive to its canonical role as a growth factor, we observed immediate and massive death of SVZ cells in PDGF-AA. Wild-type cells did not survive in PDGF-AA. However, a small fraction of null cells evaded apoptosis, displayed attenuated proliferation, gradually accumulated whole chromosome gains and losses, and, signalled by sudden rapid proliferation and growth factor independence, became tumorigenic in immune-competent syngeneic mice. Transformed cells had an OPC-like profile, were resistant to PDGFR- inhibition, and harboured highly abnormal karyotypes similar to those seen in human GBMs. ConclusionThis model associates genome instability in SVZ cells with chronic exposure to PDGF-AA; it is the first model to replicate the genomic landscape of GBM and first in which the earliest phases of GBM can be directly observed. IMPORTANCE OF STUDYWe have developed a mouse model in which the initiation, evolution and genomic landscape of GBM can be thoroughly studied thus paving the way for ideas about how this deadly brain cancer might be prevented, interrupted at an occult stage, or treated with very different therapies.

cancer biology↗