Targeting myeloid-derived suppressor cells by inhibiting hypoxia-inducible factor 1α could improve tumor progression

被引:1
作者
Xu, Qiying [1 ,2 ,3 ]
Liu, Huifang [1 ,2 ,3 ]
Song, Xiaoyan [1 ,2 ]
Wuren, Tana [1 ,2 ]
Ge, Ri-li [1 ,2 ]
机构
[1] Qinghai Univ, Res Ctr High Altitude Med, Xining, Peoples R China
[2] Qinghai Univ, Key Lab Applicat High Altitude Med, Xining, Peoples R China
[3] Qinghai Univ, Affiliated Hosp, Dept Gynecol, Xining, Peoples R China
来源
ANNALS OF MEDICINE AND SURGERY | 2024年 / 86卷 / 08期
关键词
cancer outcomes; hypoxia-inducible factor 1 alpha; LW-6; myeloid-derived suppressor cells; tumor microenvironment; DISEASE PROGRESSION;
D O I
10.1097/MS9.0000000000002126
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Myeloid-derived suppressor cells (MDSCs) are a subset of immature myeloid cells that inhibit anti-tumor immunity and contribute to poor cancer outcomes. In this study, the authors used multi-color flow cytometry to detect changes in MDSCs in patients with cancer and tumor-bearing mice. Then the authors studied changes in MDSCs ratio and mouse tumors after administration of hypoxia-inducible factor 1 alpha (HIF-1 alpha) inhibitor. The results showed that the ratio of MDSCs, specifically polymorphonuclear MDSCs (PMN-MDSCs), was higher in patients with cancer, and both PMN-MDSCs and monocytic MDSCs (M-MDSCs) ratio were higher in tumor-bearing mice. When provided with the HIF-1 alpha inhibitor LW-6, the ratio of MDSCs decreased in tumor-bearing mice, particularly PMN-MDSCs, and the volume of liver metastases also decreased. The authors' findings suggest that reducing MDSCs by inhibiting hypoxia-inducible factor 1 alpha may slow tumor progression.
引用
收藏
页码:4449 / 4455
页数:7
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