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Increased inflammatory lipid metabolism and anaplerotic mitochondrial activation follow acquired resistance to vemurafenib in BRAF-mutant melanoma cells.

Teresa Delgado-GoñiTeresa Casals GalobartSlawomir WantuchDeimante NormantaiteMartin O LeachSteven R WhittakerMounia Beloueche-Babari
Published in: British journal of cancer (2019)
Altogether, our data highlight heterogeneity in metabolic adaptations during acquired resistance to vemurafenib in BRAF-mutant melanoma, potentially uncovering key clinically-relevant mechanisms for combinatorial therapeutic targeting.
Keyphrases
  • wild type
  • oxidative stress
  • metastatic colorectal cancer
  • electronic health record
  • high intensity
  • cancer therapy
  • fatty acid