Tissue-colonizing disseminated tumor cells secrete prostaglandin E2 to promote NK cell dysfunction and evade anti-metastatic immunity

Natural killer (NK) cells are critical for anti-metastatic immunity and can eliminate metastasizing tumor cells within circulation and sites of metastatic seeding. Here, we show that disseminated tumor cells (DTCs) colonizing the mouse lung secrete prostaglandin E2 (PGE<sub>2</sub>) to locally induce NK cell dysfunction, allowing outgrowing metastases to escape immune control and establish metastatic disease. Mechanistically, PGE<sub>2</sub> signaling through its receptors EP2 and EP4 mediates NK cell dysfunction, which leads to reprogramming of NK cell gene expression and results in impaired production of anti-metastatic cytokines. In human cancer patients, the PGE<sub>2</sub>-EP2/EP4 axis is associated with NK cell dysfunction within distant organ metastases. Disabling EP2/EP4 signaling in NK cells prevents their dysfunction in DTC-colonized lungs and achieves effective NK cell-mediated control of metastatic disease. Our findings reveal a suppressive signaling axis exploited by metastasizing tumor cells to escape immune control in distant organs that could be targeted for metastatic cancer therapy.

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Publication Details

Journal
Cell Reports
Published
2024-11-01
DOI
https://doi.org/10.1016/j.celrep.2024.114855
Citations
13
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
3.13

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article

Tissue-colonizing disseminated tumor cells secrete prostaglandin E2 to promote NK cell dysfunction and evade anti-metastatic immunity

Simon Grassmann, Anna Hirschberger, Christine Klement, Tobias Bald et al.
13 citations
Cell Reports
Immune Cell Function and Interaction
3.13
article

Tissue-colonizing disseminated tumor cells secrete prostaglandin E2 to promote NK cell dysfunction and evade anti-metastatic immunity

Simon Grassmann, Anna Hirschberger, Christine Klement, Tobias Bald, Hyunu Kim, Jan P. Böttcher, Gabriela M. Wiedemann, Joseph A. Trapani, Bastian Höchst, Rupert Öllinger, Daniel Hartmann, Norbert Hüser, Joseph C. Sun, Tobias Baumann, Alfred Zippelius, Anna‐Marie Pedde, Sainitin Donakonda, Roland Rad, Felix Bayerl, Philippa Meiser, Melanie Laschinger
article en
13 citations

Abstract

Natural killer (NK) cells are critical for anti-metastatic immunity and can eliminate metastasizing tumor cells within circulation and sites of metastatic seeding. Here, we show that disseminated tumor cells (DTCs) colonizing the mouse lung secrete prostaglandin E2 (PGE<sub>2</sub>) to locally induce NK cell dysfunction, allowing outgrowing metastases to escape immune control and establish metastatic disease. Mechanistically, PGE<sub>2</sub> signaling through its receptors EP2 and EP4 mediates NK cell dysfunction, which leads to reprogramming of NK cell gene expression and results in impaired production of anti-metastatic cytokines. In human cancer patients, the PGE<sub>2</sub>-EP2/EP4 axis is associated with NK cell dysfunction within distant organ metastases. Disabling EP2/EP4 signaling in NK cells prevents their dysfunction in DTC-colonized lungs and achieves effective NK cell-mediated control of metastatic disease. Our findings reveal a suppressive signaling axis exploited by metastasizing tumor cells to escape immune control in distant organs that could be targeted for metastatic cancer therapy.

Cell ReportsVol. 43(11)
Memorial Sloan Kettering Cancer Center (US), University Hospital of Basel (CH), Technical University of Munich (DE)
Deutsche Forschungsgemeinschaft, Deutsche Krebshilfe, Elitenetzwerk Bayern
Openalex Percentile: Top 8%
Immune Cell Function and Interaction
3.13
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