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Updated: May 18, 2026

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Published on: April 7, 2017
Phenotypic plasticity of MDSC in cancers
1Department of Microbiology & Immunology, Virginia Commonwealth University, Massey Cancer Center, Richmond, Virginia 232989, USA. mmanjili@vcu.edu
Myeloid-derived suppressor cells (MDSCs) can suppress or support anti-tumor immunity due to their adaptable nature. Understanding this plasticity is key to manipulating MDSCs for better cancer treatment outcomes.
Area of Science:
- Immunology
- Oncology
- Cell Biology
Background:
- Myeloid-derived suppressor cells (MDSCs) are traditionally known for suppressing adaptive immune responses in cancer and other diseases.
- Recent findings indicate that MDSCs can also exhibit anti-tumor properties, complicating their role in disease pathology.
Purpose of the Study:
- To review the dual functions of MDSCs in the context of immune responses.
- To explore the concept of phenotypic plasticity as the underlying mechanism for these opposing roles.
- To discuss the potential for therapeutic manipulation of MDSCs.
Main Methods:
- This mini-review synthesizes existing research on MDSC function and plasticity.
- Analysis of literature focusing on the phenotypic and functional diversity of myeloid cells.
Main Results:
- MDSC functions are not fixed; they exhibit significant phenotypic plasticity.
- Environmental cues dictate the morphology, physiological state, and function of myeloid cells, including MDSCs.
- This plasticity explains the observed contradictory roles of MDSCs in anti-tumor immunity.
Conclusions:
- The opposing functions of MDSCs stem from their inherent phenotypic plasticity.
- Targeting this plasticity with immune modulators offers a potential strategy to enhance anti-tumor immune responses.
- Further research into MDSC manipulation could lead to novel cancer immunotherapies.
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