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Multi-omics-constrained kinetic models quantify pathway rewiring and predict metabolic vulnerabilities in BRCA1-deficient ovarian cancer

Cell Systems · By Ilias Toumpe, Maria Masid, Vassily Hatzimanikatis & Ljubisa Miskovic ·

The Brief

  • Toumpe et al. built multi-omics-constrained, near-genome-scale kinetic ensembles for BRCA1-associated ovarian cancer metabolism.
  • The models prioritize 28 enzyme-mediated vulnerabilities.
  • The models predict target- and physiology-specific metabolic responses and identify a shared pathway-level pattern.

Why it matters

The study offers a computational framework for linking multi-omics data to kinetic models of cancer metabolism, which could help researchers choose enzyme targets for BRCA1-deficient ovarian cancer to test experimentally.

Who’s affected

  • cancer biologists and metabolism researchers
  • systems biologists working on kinetic modelling

Toumpe et al. construct multi-omics-constrained, near-genome-scale kinetic ensembles for BRCA1-associated ovarian cancer metabolism. The models prioritize 28 enzyme-mediated vulnerabilities, predict target- and physiology-specific metabolic responses, identify a shared…

Timeline

  1. Study published in Cell Systems

  2. cell.com

    Multi-omics-constrained kinetic models quantify pathway rewiring and predict metabolic vulnerabilities in BRCA1-deficient ovarian cancer

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