Resistance to natural killer cell immunosurveillance confers a selective advantage to polyclonal metastasis
Autor: | Hin Ching Lo, Hai Wang, Weijie Zhang, Jeffrey M. Rosen, Bradley Pingel, Jun Liu, Silke Paust, Zhan Xu, Xiang Zhang, Srikanth Kodali, Ik Sun Kim, Joel R. Neilson, Sarah Hein, Sergio Aguirre, Alexander S. Krupnick, Aaron M. Muscarella |
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Rok vydání: | 2019 |
Předmět: |
Cancer Research
Lung Neoplasms biology Mesenchymal stem cell Cell Cell Count Neoplastic Cells Circulating Natural killer cell Immunosurveillance Killer Cells Natural Mice Cell killing medicine.anatomical_structure Circulating tumor cell Oncology Polyclonal antibodies Monitoring Immunologic Monoclonal medicine biology.protein Cancer research Animals |
Zdroj: | Nature cancer. 1(7) |
ISSN: | 2662-1347 |
Popis: | Polyclonal metastases frequently arise from clusters of circulating tumor cells (CTCs). CTC clusters metastasize better than single CTCs, but the underlying molecular mechanisms are poorly understood. Here, we show that polyclonal metastatic seeds exhibit higher resistance to natural killer (NK) cell killing. Using breast cancer models, we observed higher proportions of polyclonal lung metastasis in immunocompetent mice compared with mice lacking NK cells. Depleting NK cells selectively increased monoclonal but not polyclonal metastases, suggesting that CTC clusters are less sensitive to NK-mediated suppression. Transcriptional analyses revealed that clusters have elevated expression of cell–cell adhesion and epithelial genes, which is associated with decreased expression of NK cell activating ligands. Furthermore, perturbing tumor cell epithelial status altered NK ligand expression and sensitivity to NK-mediated killing. Collectively, our findings show that NK cells can determine the fate of CTCs of different epithelial and mesenchymal states, and impact metastatic clonal evolution by favoring polyclonal seeding. Zhang and colleagues report that multicellular clusters of circulating tumor cells are more resistant to killing by natural killer (NK) cells through altered NK ligand expression, resulting in polyclonal metastases. |
Databáze: | OpenAIRE |
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