Myeloid-derived suppressor cells and tumor: Current knowledge and future perspectives.
Elahe Safari1, Sajjad Ghorghanlu2, Homayoun Ahmadi-Khiavi3
1Department of Immunology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Myeloid-derived suppressor cells (MDSCs) promote cancer progression and immunotherapy resistance. Targeting MDSC development and infiltration offers a promising therapeutic strategy for various cancers.
Area of Science:
- Immunology
- Oncology
- Cancer Research
Background:
- Tumor lesions exhibit immunosuppressive properties, hindering effective cancer immunotherapy.
- Chronic inflammation, driven by stromal and tumor cells, generates immunosuppressive factors.
- These factors induce myeloid-derived suppressor cells (MDSCs), key mediators of tumor immunosuppression.
Purpose of the Study:
- To review recent findings on the role of MDSCs in tumor progression.
- To discuss potential therapeutic strategies targeting MDSCs for cancer treatment.
Main Methods:
- Literature review of studies on MDSCs in cancer progression and immunotherapy.
- Analysis of clinical data correlating MDSC frequency with cancer stage and therapeutic response.
Main Results:
- MDSCs are crucial for tumor immunosuppression, requiring direct cell-to-cell contact for function.
- Peripheral blood MDSC frequency correlates with clinical stage and treatment outcomes in various cancers.
- MDSCs contribute to chemoresistance in cancer settings.
Conclusions:
- Blocking the cycle of MDSC development and infiltration is a rational therapeutic approach.
- Targeting MDSCs holds potential for future clinical trials to improve cancer therapy.
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