Targeting extracellular nutrient dependencies of cancer cells

Javier Garcia-Bermudez, Robert T. Williams, Rohiverth Guarecuco, Kıvanç Birsoy

Research output: Contribution to journalReview articlepeer-review

29 Scopus citations

Abstract

Background: Cancer cells rewire their metabolism to meet the energetic and biosynthetic demands of their high proliferation rates and environment. Metabolic reprogramming of cancer cells may result in strong dependencies on nutrients that could be exploited for therapy. While these dependencies may be in part due to the nutrient environment of tumors, mutations or expression changes in metabolic genes also reprogram metabolic pathways and create addictions to extracellular nutrients. Scope of review: This review summarizes the major nutrient dependencies of cancer cells focusing on their discovery and potential mechanisms by which metabolites become limiting for tumor growth. We further detail available therapeutic interventions based on these metabolic features and highlight opportunities for restricting nutrient availability as an anti-cancer strategy. Major conclusions: Strategies to limit nutrients required for tumor growth using dietary interventions or nutrient degrading enzymes have previously been suggested for cancer therapy. The best clinical example of exploiting cancer nutrient dependencies is the treatment of leukemia with L-asparaginase, a first-line chemotherapeutic that depletes serum asparagine. Despite the success of nutrient starvation in blood cancers, it remains unclear whether this approach could be extended to other solid tumors. Systematic studies to identify nutrient dependencies unique to individual tumor types have the potential to discover targets for therapy.

Original languageEnglish (US)
Pages (from-to)67-82
Number of pages16
JournalMolecular Metabolism
Volume33
DOIs
StatePublished - Mar 2020
Externally publishedYes

Keywords

  • Amino acids
  • Asparaginase
  • Cancer metabolism
  • Diet
  • Metabolic therapy
  • Nutrient dependencies

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

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