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Chimera and Tandem-Repeat Type Galectins: The New Targets for Cancer Immunotherapy
Frankie Chi Fat Ko1, Sheng Yan1, Ka Wai Lee2
1Department of Medicine, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Queen Mary Hospital, 102 Pokfulam Road, Hong Kong, China.
Galectins regulate immune responses in the tumor microenvironment. Inhibitors like GB1211 and LYT-200 show promise in clinical trials, potentially enhancing cancer immunotherapy by modulating immune cells.
Area of Science:
- Immunology
- Oncology
- Molecular Biology
Background:
- Galectins are a family of 12 proteins in humans with diverse intracellular and extracellular functions.
- They critically influence the tumor microenvironment (TME) by modulating immune cell infiltration and function.
- Cancer cells can exploit the pro-tumorigenic activities of immune cells, highlighting the need for targeted therapies.
Purpose of the Study:
- To review the biological functions of human galectins, focusing on their roles in cancer immunity.
- To discuss the therapeutic potential of galectin inhibitors, such as GB1211 and LYT-200, in clinical trials.
- To explore the combined use of galectin inhibitors with immune checkpoint inhibitors (ICIs) for enhanced anti-cancer effects.
Main Methods:
- Comprehensive literature review of galectin functions in cancer immunology.
- Analysis of current clinical trial data for galectin inhibitors GB1211 and LYT-200.
- Discussion of downstream effects of galectin inhibition on various immune cell populations.
Main Results:
- Galectins modulate immune responses, affecting T cells, macrophages, and neutrophils within the TME.
- Galectin-3 and -9 inhibitors (GB1211, LYT-200) are advancing in clinical trials for cancer treatment.
- Inhibition of galectins demonstrates broad effects on immune cells, including enhancing cytotoxic T cell activity and reducing T cell exhaustion.
Conclusions:
- Galectins are key regulators of anti-tumor immunity, offering therapeutic targets.
- Galectin inhibitors represent a promising strategy, particularly in combination with ICIs.
- Further research into galectin biology and inhibitor limitations is crucial for optimizing clinical applications.
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