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Metabolic networks in the tumor microenvironment: roles of amino acid and lipid metabolism pathways in cancer progression and therapy

  • 작성자

    Jung Min Han
  • 작성일자

    2026-07-24
  • 조회수

    484
Jung Min Han Jung Min Han (jhan74@yonsei.ac.kr)
2002-2008 Principal Investigator, Imagene, Co. Ltd.
2008-2011 Research assistant professor, Research Institute of Pharmaceutical Sciences, Seoul National University
2011-2013 Research associate professor, Medicinal Bioconvergence Research Center, Seoul National University
2011-2013 Principal Investigator/Drug Screening group leader, Medicinal Bioconvergence Research Center, Seoul National University
2015-2017 Bioconvergence major chair, Integrated Science and Engineering Field, Underwood International College, Yonsei University
2013-2020 Associate professor, College of Pharmacy, Yonsei University
2013-2020 Associate professor, WCU Integrated OMICS for Biomedical Science, Yonsei University
2020-present Professor, College of Pharmacy, Yonsei University
2020-present Professor, WCU Integrated OMICS for Biomedical Science, Yonsei University
2024-present Professor, Department of Integrated Biotechnology, Yonsei University
2021-2025 Affiliate faculty, POSTECH Biotech Center, POSTECH
2024-2026 Associate Dean, College of Pharmacy, Yonsei University
2026-present Head, Graduate Program in Pharmacy, College of Pharmacy, Yonsei University

Metabolic networks in the tumor microenvironment: roles of amino acid and lipid metabolism pathways in cancer progression and therapy

Metabolic rewiring, a defining hallmark of cancer, sustains cell proliferation and biosynthesis while coordinating adaptive interactions within the tumor microenvironment (TME). Recent advances reveal that metabolism in the TME-comprising stromal, immune and endothelial components forms a complex metabolic network in which intercellular competition, cooperation and plasticity profoundly influence tumor progression and therapeutic responses. Here we integrate emerging evidence on the organizational principles of amino acid and lipid metabolism within the TME, emphasizing how nutrient fluxes shape immune evasion, therapeutic resistance and metabolic symbiosis. We highlight key mechanisms through which cancer and nonmalignant cells engage in reciprocal nutrient manipulation, focusing on glutamine, arginine, tryptophan, branched-chain amino acids and lipids. The dual roles of these metabolites in immune regulation and tumor growth reveal the limitations of traditional single-pathway targeting and advocate for a network-centric therapeutic approach. We further discuss how metabolite-derived signaling and epigenetic regulation reinforce cell state transitions and immune suppression. Current and emerging therapeutic strategies, including multitarget combinations and immune-metabolic synergies, are evaluated alongside translational challenges. Finally, we underscore the need for spatial metabolomics, liquid biopsy platforms and artificial intelligence-driven modeling to map nutrient competition and cooperative exchange within the TME, offering new opportunities for precision metabolic interventions.

Exp Mol Med. 2026 Apr;58(4):1128-1148. doi: 10.1038/s12276-026-01697-0
https://pubmed.ncbi.nlm.nih.gov/41826648/