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Unveiling the role of taurine and SLC6A6 in tumor immune evasion: Implications for gastric cancer therapy.
- Source :
-
International Journal of Biochemistry & Cell Biology . Nov2024, Vol. 176, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- Metabolic changes are key drivers of tumor progression. Understanding how metabolic reprogramming promotes tumor development and identifying key metabolic activities are essential for improving tumor diagnosis and treatment. Among the numerous transporters in the body, solute carriers (SLCs) are particularly significant, often overexpressed in cancer cells to meet the tumor's demand for nutrients and energy. While the role of SLCs in nutrient absorption within the gastrointestinal tract is well-established, their specific role in gastric cancer (GC) remains unclear. Recently, Xiaodi Zhao's team investigated the critical role of taurine and its transporter, SLC6A6, in anti-tumor immunity and clinical outcomes. Notably, this research marks the first instance of taurine exhibiting a dual role. It promotes tumor growth in immunodeficient mice while inhibiting it in immunocompetent mice. The study found that taurine exerts its anti-cancer effects by modulating CD8+ T cells rather than directly inhibiting tumor cells, revealing the SP1-SLC6A6 axis as a key mechanism behind chemotherapy-induced immune evasion. Our work further explored the potential, advantages, and challenges of using taurine and SLC6A6 as biomarkers and therapeutic targets in gastric cancer. We aim to underscore their importance in both basic research and clinical applications, providing valuable insights and guidance for future investigations. [ABSTRACT FROM AUTHOR]
- Subjects :
- *METABOLIC reprogramming
*STOMACH cancer
*T cells
*TAURINE
*TUMOR growth
Subjects
Details
- Language :
- English
- ISSN :
- 13572725
- Volume :
- 176
- Database :
- Academic Search Index
- Journal :
- International Journal of Biochemistry & Cell Biology
- Publication Type :
- Academic Journal
- Accession number :
- 180585284
- Full Text :
- https://doi.org/10.1016/j.biocel.2024.106661