TRAIL-dependent apoptosis of peritoneal mesothelial cells by NK cells promotes ovarian cancer invasion

• Published in: iScience Vol. 26; no. 12; p. 108401
• Main Authors: Steitz, Anna Mary, Schröder, Clarissa, Knuth, Isabel, Keber, Corinna U., Sommerfeld, Leah, Finkernagel, Florian, Jansen, Julia M., Wagner, Uwe, Müller-Brüsselbach, Sabine, Worzfeld, Thomas, Huber, Magdalena, Beutgen, Vanessa M., Graumann, Johannes, Pogge von Strandmann, Elke, Müller, Rolf, Reinartz, Silke
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 15-12-2023; Elsevier
• Subjects: Cancer; Immunology; Microenvironment; Immunology; Microenvironment; Cancer
• ISSN: 2589-0042; 2589-0042
• DOI: 10.1016/j.isci.2023.108401

A crucial requirement for metastasis formation in ovarian high-grade serous carcinoma (HGSC) is the disruption of the protective peritoneal mesothelium. Using co-culture systems of primary human cells, we discovered that tumor-associated NK cells induce TRAIL-dependent apoptosis in mesothelial cells via death receptors DR4 and DR5 upon encounter with activated T cells. Upregulation of TRAIL expression in NK cells concomitant with enhanced cytotoxicity toward mesothelial cells was driven predominantly by T-cell-derived TNFα, as shown by affinity proteomics-based analysis of the T cell secretome in conjunction with functional studies. Consistent with these findings, we detected apoptotic mesothelial cells in the peritoneal fluid of HGSC patients. In contrast to mesothelial cells, HGSC cells express negligible levels of both DR4 and DR5 and are TRAIL resistant, indicating cell-type-selective killing by NK cells. Our data point to a cooperative action of T and NK in breaching the mesothelial barrier in HGSC patients.
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•Cancer-associated NK cells induce TRAIL-dependent apoptosis in mesothelial cells•Induction of apoptosis by NK cells is mainly driven by T-cell-derived TNFα•NK-cell-mediated mesothelial cell death promotes ovarian cancer cell invasion•Low TRAIL receptor levels on cancer cells contribute to their TRAIL resistance
Microenvironment; Immunology; Cancer