Bi-directional metabolic reprogramming between cancer cells and T cells reshapes the anti-tumor immune response
Cancer cells and T cells engage in dynamic crosstalk within the tumor microenvironment (TME), shaping tumor progression and anti-tumor immunity. While cancer cells reprogram metabolism to support growth and immune evasion, T cells must adapt their metabolic states to maintain effector functions. Tumor-driven metabolic perturbations, such as nutrient depletion and accumulation of immunosuppressive metabolites, profoundly impair T cell function and fate. Conversely, metabolically reprogrammed T cells can modulate the TME and influence tumor growth. This reciprocal metabolic crosstalk represents both metabolic competition and intercellular communication, offering promising therapeutic targets.
Authors
- Guideng Li (ORCID: https://orcid.org/0000-0003-0840-7262)
- Hongcheng Cheng
- Yajing Qiu (ORCID: https://orcid.org/0000-0002-2628-254X)
- Xinyuan Ding (ORCID: https://orcid.org/0000-0002-8982-6807)
- Congcong Zhao
- Yihan Xu (ORCID: https://orcid.org/0000-0001-6537-0326)
Institutions
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Suzhou Municipal Hospital (CN)
- Suzhou Institute of Systems Medicine (CN)
Publication Details
- Journal
- PLoS Biology
- Published
- 2025-07-14
- DOI
- https://doi.org/10.1371/journal.pbio.3003284
- Citations
- 7
- Primary Topic
- Cancer, Hypoxia, and Metabolism
- Type
- article
- Field-Weighted Citation Impact
- 6.55
Funders
- National Natural Science Foundation of China
- Natural Science Foundation of Jiangsu Province