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               <dc:title>Analysing metabolic changes in a gastric adenocarcinoma cell line under different drug treatments: a constraint-based modeling approach</dc:title>
               <dc:creator>Benedicto Molina, Xavier</dc:creator>
               <dc:creator>Ponce De Leon, Miguel</dc:creator>
               <dc:subject>Àrees temàtiques de la UPC::Informàtica::Arquitectura de computadors</dc:subject>
               <dc:subject>High performance computing</dc:subject>
               <dc:subject>gastric carcinoma</dc:subject>
               <dc:subject>drug synergies</dc:subject>
               <dc:subject>AGS</dc:subject>
               <dc:subject>metabolic tasks</dc:subject>
               <dc:subject>genome-scale metabolic models</dc:subject>
               <dc:subject>Càlcul intensiu (Informàtica)</dc:subject>
               <dc:description>Gastric carcinoma (GC) is one of the leading causes&#xd;
of cancer death globally. Managing advanced stages of GC&#xd;
necessitates a multifaceted approach, encompassing surgical&#xd;
interventions and comprehensive multidisciplinary strategies&#xd;
such as combinatorial drug treatments, recently emerging as&#xd;
promising avenues. Recent advances in computational biology&#xd;
have facilitated the development of genome-scale metabolic&#xd;
models (GEMs), which offer a comprehensive, mathematical&#xd;
framework for understanding the intricate metabolic dynamics.&#xd;
Integrating these GEMs with high-throughput omics&#xd;
data, GEMs provide a representations of cellular metabolism&#xd;
through metabolic tasks, allowing for the elucidation of complex&#xd;
metabolic phenotypes associated with the effects of combinatorial&#xd;
treatments. Herein, an approach to take advantage of&#xd;
metabolic tasks and high-throughput omics data using the previously&#xd;
described Tasks Inferred from Differential Expression&#xd;
(TIDEs) approach in conjunction with vital genes to metabolic&#xd;
tasks (anchor genes) is presented as ag-TIDEs.&#xd;
The aim of this work is to explore aberrant metabolic&#xd;
phenotypes using different approaches to generate hypotheses&#xd;
on the mechanisms underlying the observed synergies in the&#xd;
combinatorial drug treatments of TAK1, MEK, and PI3K&#xd;
inhibitors on cells from the AGS cell line. Preliminary results&#xd;
propose distinct metabolic alterations induced by the drug&#xd;
treatments as a hypothesis to be further explored.</dc:description>
               <dc:date>2023-05</dc:date>
               <dc:type>Conference report</dc:type>
               <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
               <dc:rights>Open Access</dc:rights>
               <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
               <dc:publisher>Barcelona Supercomputing Center</dc:publisher>
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