Myeloid-Derived Suppressor Cells in the Tumor Microenvironment

被引:159
|
作者
Dysthe, Matthew [1 ,2 ,3 ]
Parihar, Robin [2 ,3 ,4 ]
机构
[1] Baylor Coll Med, Translat Biol & Mol Med Grad Program, Houston, TX 77030 USA
[2] Houston Methodist Hosp, Texas Childrens Hosp, Ctr Cell & Gene Therapy, Houston, TX 77030 USA
[3] Baylor Coll Med, Houston, TX 77030 USA
[4] Baylor Coll Med, Dept Pediat, Sect Hematol Oncol, Houston, TX 77030 USA
关键词
Myeloid-derived suppressor cells (MDSC); Cancer; Tumor microenvironment (TME); Immunosuppression; Solid tumor; Myelopoiesis; Angiogenesis; Metastasis; Autoimmunity; Therapy resistance; Therapeutic strategies; STAT3; S100A9; Transforming growth factor (TGF)-beta; Arginase-1; Regulatory T cells (Treg); ENDOTHELIAL GROWTH-FACTOR; REGULATORY T-CELLS; TRANS-RETINOIC ACID; BONE-MARROW; ANTITUMOR IMMUNITY; PERIPHERAL-BLOOD; TGF-BETA; GM-CSF; PROGENITOR CELLS; PROSTATE-CANCER;
D O I
10.1007/978-3-030-35723-8_8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Myeloid-derived suppressor cells (MDSCs) represent a heterogenous population of immature myeloid cells capable of modulating immune responses. In the context of cancer, MDSCs are abnormally produced and recruited to the tumor microenvironment (TME) to aid in the establishment of an immunosuppressive TME that facilitates tumor escape. Additionally, MDSCs contribute to non-immunologic aspects of tumor biology, including tumor angiogenesis and metastasis. The clinical significance of MDSCs has recently been appreciated as numerous studies have suggested a correlation between circulating and intratumoral MDSC frequencies and tumor stage, progression, and treatment resistance. In this chapter, we review MDSC characterization, development, expansion, and mechanisms that facilitate immunosuppression and tumor progression. Furthermore, we highlight studies demonstrating the clinical significance of MDSCs in various disease states in addition to strategies that modulate various aspects of MDSC biology for therapeutic gain.
引用
收藏
页码:117 / 140
页数:24
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