TRAIL-induced cytokine production via NFKB2 pathway promotes neutrophil chemotaxis and immune suppression in triple negative breast cancers

Kundu, M.; Greer, Y. E.; Lobanov, A.; Ridnour, L.; Donahue, R. N.; Ng, Y.; Ratnayake, S.; Voeller, D.; Weltz, S.; Chen, Q.; Lockett, S. J.; Cam, M.; Meerzaman, D.; Wink, D. A.; Lipkowitz, S.

doi:10.1101/2024.07.19.604341

bioRxiv · 10.1101/2024.07.19.604341

TRAIL-induced cytokine production via NFKB2 pathway promotes neutrophil chemotaxis and immune suppression in triple negative breast cancers

Kundu, M.·Greer, Y. E.·Lobanov, A.·Ridnour, L.·Donahue, R. N.·Ng, Y.·Ratnayake, S.·Voeller, D.·Weltz, S.·Chen, Q.·Lockett, S. J.·Cam, M.·Meerzaman, D.·Wink, D. A.·Lipkowitz, S.

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Abstract

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is a potential cancer therapeutic that induces apoptosis in cancer cells while sparing the non-malignant cells in preclinical models. However, its efficacy in clinical trials has been limited, suggesting unknown modulatory mechanisms responsible for the lack of TRAIL activity in patients. Here, we hypothesized that TRAIL treatment elicits transcriptional changes in triple negative breast cancer (TNBC) cells that alter the immune milieu. To test this, we performed an RNAseq analysis of MDA-MB-231 cells treated with TRAIL, followed by validation in additional TNBC cell lines. TRAIL significantly induces expression of multiple cytokines such as CXCLs 1, 2, 3, 8,11 and IL-6, which are known to modify neutrophil function. Mechanistically, the induction of these cytokines was predominantly mediated by death receptor 5, caspase 8 (but not caspase 8 enzymatic activity), and the non-canonical NFKB2 pathway. The cytokines produced by the TRAIL-treated TNBC cells enhanced chemotaxis of healthy human donor isolated neutrophils. In vivo, TRAIL treated TNBC murine xenograft tumors showed activation of the NFKB2 pathway, elevated production of CXCLs and IL-6, and increased neutrophil recruitment into the tumors. Moreover, donor isolated neutrophils preincubated in supernatants from TRAIL-treated TNBC cells exhibited impaired cytotoxic effect against TNBC cells. Transcriptomic analysis of neutrophils incubated with either TRAIL alone or supernatant of TRAIL-treated TNBC cells revealed increased expression of inflammatory cytokines, immune modulatory genes, immune checkpoint genes, and genes implicated in delayed neutrophil apoptosis. Functional studies with these neutrophils confirmed their suppressive effect on T cell proliferation and an increase in Treg suppressive phenotype. Collectively, our study demonstrates a novel role of TRAIL-induced NFKB2-dependent cytokine production that promotes neutrophil chemotaxis and immune suppression.

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Kundu, M., Greer, Y. E., Lobanov, A., Ridnour, L., Donahue, R. N., Ng, Y., Ratnayake, S., Voeller, D., Weltz, S., Chen, Q., Lockett, S. J., Cam, M., Meerzaman, D., Wink, D. A., Lipkowitz, S.. 2024-07-23. TRAIL-induced cytokine production via NFKB2 pathway promotes neutrophil chemotaxis and immune suppression in triple negative breast cancers. https://doi.org/10.1101/2024.07.19.604341

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