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Neural hijacking in cancer metabolism: from nutrients to organelles.

Trends in cancer 2026 Vol.12(3) p. 221-234

Shin S, Myoung SY, Cho HJ, Kim S, Lee N, Park SJ

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Tumors dynamically interact with the central and peripheral nervous systems, hijacking neural plasticity and reprogramming metabolism in a bidirectional manner to drive cancer progression.

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APA Shin S, Myoung SY, et al. (2026). Neural hijacking in cancer metabolism: from nutrients to organelles.. Trends in cancer, 12(3), 221-234. https://doi.org/10.1016/j.trecan.2025.11.006
MLA Shin S, et al.. "Neural hijacking in cancer metabolism: from nutrients to organelles.." Trends in cancer, vol. 12, no. 3, 2026, pp. 221-234.
PMID 41318256

Abstract

Tumors dynamically interact with the central and peripheral nervous systems, hijacking neural plasticity and reprogramming metabolism in a bidirectional manner to drive cancer progression. Neural inputs reshape the metabolism of cancer cells and their microenvironment - glycolysis, oxidative phosphorylation, and lipid metabolism - while tumors exploit neuronal nutrients and mitochondria to thrive under metabolic stress. This review explores neurocancer metabolic crosstalk through multiple mechanisms by three principal modes of interaction, highlighting how targeting these metabolic interdependencies could disrupt tumor progression. By integrating cancer metabolism and neuroscience, it offers a conceptual framework for understanding neural-tumor metabolic circuits in malignancy and identifies potential therapeutic vulnerabilities.

MeSH Terms

Humans; Neoplasms; Tumor Microenvironment; Mitochondria; Glycolysis; Nutrients; Animals; Lipid Metabolism; Oxidative Phosphorylation; Neuronal Plasticity; Neurons; Energy Metabolism

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