| Literature DB >> 31835202 |
Bao-Hua Li1, Malgorzata A Garstka2, Zong-Fang Li3.
Abstract
Myeloid-derived suppressor cells (MDSCs) expand in tumor-bearing host. They suppress anti-tumor immune response and promote tumor growth. Chemokines play a vital role in recruiting MDSCs into tumor tissue. They can also induce the generation of MDSCs in the bone marrow, maintain their suppressive activity, and promote their proliferation and differentiation. Here, we review CCL2/CCL12-CCR2, CCL3/4/5-CCR5, CCL15-CCR1, CX3CL1/CCL26-CX3CR1, CXCL5/2/1-CXCR2, CXCL8-CXCR1/2, CCL21-CCR7, CXCL13-CXCR5 signaling pathways, their role in MDSCs recruitment to tumor tissue, and their correlation with tumor development, metastasis and prognosis. Targeting chemokines and their receptors may serve as a promising strategy in immunotherapy, especially combined with other strategies such as chemotherapy, cyclin-dependent kinase or immune checkpoints inhibitors.Entities:
Keywords: Cancer immunotherapy; Chemo-attractant cytokines; Immunosuppression; MDSCs; Therapeutic targeting; Tumor microenvironment
Mesh:
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Year: 2019 PMID: 31835202 DOI: 10.1016/j.molimm.2019.11.014
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407