» Articles » PMID: 38191922

Myeloid-derived Suppressor Cells in Cancer and Cancer Therapy

Overview
Specialty Oncology
Date 2024 Jan 9
PMID 38191922
Authors
Affiliations
Soon will be listed here.
Abstract

Anticancer agents continue to dominate the list of newly approved drugs, approximately half of which are immunotherapies. This trend illustrates the considerable promise of cancer treatments that modulate the immune system. However, the immune system is complex and dynamic, and can have both tumour-suppressive and tumour-promoting effects. Understanding the full range of immune modulation in cancer is crucial to identifying more effective treatment strategies. Myeloid-derived suppressor cells (MDSCs) are a heterogeneous population of myeloid cells that develop in association with chronic inflammation, which is a hallmark of cancer. Indeed, MDSCs accumulate in the tumour microenvironment, where they strongly inhibit anticancer functions of T cells and natural killer cells and exert a variety of other tumour-promoting effects. Emerging evidence indicates that MDSCs also contribute to resistance to cancer treatments, particularly immunotherapies. Conversely, treatment approaches designed to eliminate cancer cells can have important additional effects on MDSC function, which can be either positive or negative. In this Review, we discuss the interplay between MDSCs and various other cell types found in tumours as well as the mechanisms by which MDSCs promote tumour progression. We also discuss the relevance and implications of MDSCs for cancer therapy.

Citing Articles

Harnessing myeloid cells in cancer.

Park S, Pylaeva E, Bhuria V, Gambardella A, Schiavoni G, Mougiakakos D Mol Cancer. 2025; 24(1):69.

PMID: 40050933 PMC: 11887392. DOI: 10.1186/s12943-025-02249-2.


Cell-intrinsic PD-L1 signaling drives immunosuppression by myeloid-derived suppressor cells through IL-6/Jak/Stat3 in PD-L1-high lung cancer.

Jeong H, Koh J, Kim S, Yim J, Song S, Kim H J Immunother Cancer. 2025; 13(3).

PMID: 40050048 PMC: 11887297. DOI: 10.1136/jitc-2024-010612.


Myeloid cells: key players in tumor microenvironments.

Hua Q, Li Z, Weng Y, Wu Y, Zheng L Front Med. 2025; .

PMID: 40048137 DOI: 10.1007/s11684-025-1124-8.


The epigenetic hallmarks of immune cells in cancer.

Ji Y, Xiao C, Fan T, Deng Z, Wang D, Cai W Mol Cancer. 2025; 24(1):66.

PMID: 40038722 PMC: 11881328. DOI: 10.1186/s12943-025-02255-4.


Advances in Antibody-Based Immune-Stimulating Drugs: Driving Innovation in Cancer Therapy.

Zhao R, Fan X Int J Mol Sci. 2025; 26(4).

PMID: 40003906 PMC: 11855211. DOI: 10.3390/ijms26041440.


References
1.
Dunn G, Bruce A, Ikeda H, Old L, Schreiber R . Cancer immunoediting: from immunosurveillance to tumor escape. Nat Immunol. 2002; 3(11):991-8. DOI: 10.1038/ni1102-991. View

2.
Condamine T, Mastio J, Gabrilovich D . Transcriptional regulation of myeloid-derived suppressor cells. J Leukoc Biol. 2015; 98(6):913-22. PMC: 4661041. DOI: 10.1189/jlb.4RI0515-204R. View

3.
Hicks K, Tyurina Y, Kagan V, Gabrilovich D . Myeloid Cell-Derived Oxidized Lipids and Regulation of the Tumor Microenvironment. Cancer Res. 2021; 82(2):187-194. PMC: 8770601. DOI: 10.1158/0008-5472.CAN-21-3054. View

4.
Gabrilovich D, Bronte V, Chen S, Colombo M, Ochoa A, Ostrand-Rosenberg S . The terminology issue for myeloid-derived suppressor cells. Cancer Res. 2007; 67(1):425. PMC: 1941787. DOI: 10.1158/0008-5472.CAN-06-3037. View

5.
Bronte V, Brandau S, Chen S, Colombo M, Frey A, Greten T . Recommendations for myeloid-derived suppressor cell nomenclature and characterization standards. Nat Commun. 2016; 7:12150. PMC: 4935811. DOI: 10.1038/ncomms12150. View