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Microwave ablation of primary breast cancer inhibits metastatic progression in model mice via activation of natural killer cells

Authors :
Lijun Ling
Jiawei Liu
Yue Wang
Mengjia Qian
Li Li
Wenbin Zhou
Hui Xie
Mingjie Zheng
Hong Pan
Yi Zhao
Muxin Yu
Xiaoxiang Guan
Qiang Ding
Shui Wang
Cong Wang
Nan Che
Ge Ma
Source :
Cell Mol Immunol
Publication Year :
2020
Publisher :
Nature Publishing Group UK, 2020.

Abstract

Surgery is essential for controlling the symptoms and complications of stage IV breast cancer. However, locoregional treatment of primary tumors often results in distant progression, including lung metastasis, the most common type of visceral metastasis. As a minimally invasive thermal therapy, microwave ablation (MWA) has been attempted in the treatment of breast cancer, but the innate immune response after MWA has not yet been reported. Using two murine models of stage IV breast cancer, we found that MWA of primary breast cancer inhibited the progression of lung metastasis and improved survival. NK cells were activated after MWA of the primary tumor and exhibited enhanced cytotoxic functions, and the cytotoxic pathways of NK cells were activated. Depletion experiments showed that NK cells but not CD4+ or CD8+ T cells played a pivotal role in prolonging survival. Then, we found that compared with surgery or control treatment, MWA of the primary tumor induced completely different NK-cell-related cytokine profiles. Macrophages were activated after MWA of the primary tumor and produced IL-15 that activated NK cells to inhibit the progression of metastasis. In addition, MWA of human breast cancer stimulated an autologous NK-cell response. These results demonstrate that MWA of the primary tumor in metastatic breast cancer inhibits metastatic progression via the macrophage/IL-15/NK-cell axis. MWA of the primary tumor may be a promising treatment strategy for de novo stage IV breast cancer, although further substantiation is essential for clinical testing.

Details

Language :
English
Database :
OpenAIRE
Journal :
Cell Mol Immunol
Accession number :
edsair.doi.dedup.....58b6bd3e7110689feb0a1e7947b30d41