Myeloid-derived suppressor cells in cancer: Current knowledge and future perspectives.
Sunanda Rajkumari1, Jaspreet Singh2, Usha Agrawal3
1ICMR National Institute of Medical Statistics, Ansari Nagar, New Delhi 110029, India.
International Immunopharmacology
|September 5, 2024
Summary
Myeloid-derived suppressor cells (MDSCs) fuel cancer immune evasion and poor prognosis. Targeting MDSCs offers a promising strategy to improve cancer treatment outcomes and immune surveillance.
Area of Science:
- Immunology
- Oncology
- Cancer Research
Background:
- Myeloid-derived suppressor cells (MDSCs) are key players in cancer immune evasion.
- MDSCs accumulate in tumors and blood, suppressing anti-cancer immune cells like T-cells and NK cells.
- They promote tumor growth, angiogenesis, and metastasis, creating a pro-tumorigenic environment.
Purpose of the Study:
- To provide a comprehensive review of myeloid-derived suppressor cells (MDSCs) in cancer.
- To detail the regulation of MDSC development and function.
- To discuss MDSCs as prognostic/predictive biomarkers and explore therapeutic targeting strategies.
Main Methods:
- Literature review of existing research on MDSCs in cancer.
- Analysis of MDSC roles in immune suppression, angiogenesis, and metastasis.
- Examination of current and emerging therapeutic approaches targeting MDSCs.
Main Results:
- MDSC accumulation correlates with poor prognosis and therapeutic resistance in cancer patients.
- MDSCs actively suppress various immune cells, contributing to immune evasion.
- Targeting MDSCs holds potential for enhancing cancer therapy efficacy and immune surveillance.
Conclusions:
- MDSCs are critical mediators of tumor immune escape and represent a significant therapeutic target.
- Understanding MDSC regulation and function is vital for developing effective cancer treatments.
- Targeting MDSCs may improve patient outcomes by overcoming immune suppression and enhancing anti-tumor immunity.
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