Authors
Ibrahim, M., Bhoite, R., Lakshmanan, M., Raman, K.
Abstract
Cancer cells rapidly rewire their metabolism, from efficient energy production toward anabolic processes, to sustain uncontrolled growth. Decoding such metabolic shifts is essential for uncovering novel therapeutic targets. To map systems-level metabolic changes across cancer types, we built context-specific genome-scale metabolic models for eight tissues (lung, thyroid, stomach, prostate, liver, kidney, colon, and breast) using gene expression data from The Cancer Genome Atlas (TCGA). Applying constraint-based modelling, we then identified differentially regulated pathways through flux enrichment analysis, revealing tissue-specific rewiring: branched chain amino acid metabolism was suppressed in breast cancer; sphingolipid metabolism was downregulated in colon, kidney, and thyroid but upregulated in breast. We further propose a model-driven pipeline to identify and characterise metabolic vulnerabilities. We first identify synthetic lethal reactions in normal tissues and their corresponding single lethal counterparts in cancers, thereby enabling the identification of metabolic "collateral lethal" reaction pairs for each cancer. Model-predicted collateral lethal gene pairs, including CMPK1-AK in colon, ALDOA-PGD in prostate, and SLC25A26-UQCRB in liver models, were supported through computational validation using DepMap data on gene essentiality. Subsequently, we show how to interpret metabolic rewiring in cancer tissues while accounting for any collateral lethal pairs. In summary, our results establish a systemic framework for decoding metabolic rewiring and synthetic lethal vulnerabilities in cancer.
Preprint server:
bioRxiv
The authors list and abstract were imported from bioRxiv on 22 Aug 2026.
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