4.7 Review

Metabolic heterogeneity and adaptability in brain tumors

Journal

CELLULAR AND MOLECULAR LIFE SCIENCES
Volume 77, Issue 24, Pages 5101-5119

Publisher

SPRINGER BASEL AG
DOI: 10.1007/s00018-020-03569-w

Keywords

Glioma; Tumor microenvironment (TME); Metabolism; Cell communication; Tumor initiating cells; Slow-cycling cells; Immune cells

Funding

  1. American Brain Tumor Association (ABTA) Discovery Grant - Uncle Kory Foundation
  2. MRC [MR/S007709/1]
  3. Florida Center for Brain Tumor Research & Accelerate Brain Cancer Cure [P0058849]
  4. ABTA Discovery Grant [DG1800014]
  5. Pray for Dominic St Baldrick's Research Grant [638733]
  6. UFHCC Cancer Therapeutics & Host Response Research grant [00096885]
  7. Dana-Farber/Harvard Cancer Center (DF/HCC) SPORE in brain cancer DRP Award
  8. MRC [MR/S007709/1] Funding Source: UKRI

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The metabolic complexity and flexibility commonly observed in brain tumors, especially glioblastoma, is fundamental for their development and progression. The ability of tumor cells to modify their genetic landscape and adapt metabolically, subverts therapeutic efficacy, and inevitably instigates therapeutic resistance. To overcome these challenges and develop effective therapeutic strategies targeting essential metabolic processes, it is necessary to identify the mechanisms underlying heterogeneity and define metabolic preferences and liabilities of malignant cells. In this review, we will discuss metabolic diversity in brain cancer and highlight the role of cancer stem cells in regulating metabolic heterogeneity. We will also highlight potential therapeutic modalities targeting metabolic vulnerabilities and examine how intercellular metabolic signaling can shape the tumor microenvironment.

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