Cyclooxygenase-dependent tumor growth through evasion of immunity
journal contributionposted on 23.09.2020, 11:57 by Santiago Zelenay, Annemarthe G van der Veen, Jan P Böttcher, Kathryn J Snelgrove, Neil Rogers, Sophie E Acton, Probir Chakravarty, Maria Romina Girotti, Richard Marais, Sergio A Quezada, Erik Sahai, Caetano Reis e Sousa
The mechanisms by which melanoma and other cancer cells evade anti-tumor immunity remain incompletely understood. Here, we show that the growth of tumors formed by mutant Braf(V600E) mouse melanoma cells in an immunocompetent host requires their production of prostaglandin E2, which suppresses immunity and fuels tumor-promoting inflammation. Genetic ablation of cyclooxygenases (COX) or prostaglandin E synthases in Braf(V600E) mouse melanoma cells, as well as in Nras(G12D) melanoma or in breast or colorectal cancer cells, renders them susceptible to immune control and provokes a shift in the tumor inflammatory profile toward classic anti-cancer immune pathways. This mouse COX-dependent inflammatory signature is remarkably conserved in human cutaneous melanoma biopsies, arguing for COX activity as a driver of immune suppression across species. Pre-clinical data demonstrate that inhibition of COX synergizes with anti-PD-1 blockade in inducing eradication of tumors, implying that COX inhibitors could be useful adjuvants for immune-based therapies in cancer patients.
Adaptive ImmunityAnimalsAntibodies, MonoclonalAntigens, CDAspirinCell Line, TumorDendritic CellsHumansImmunity, InnateImmunotherapyInflammationIntegrin alpha ChainsInterferonsMelanomaMiceNeoplasmsProgrammed Cell Death 1 ReceptorProstaglandin-Endoperoxide SynthasesProstaglandinsProto-Oncogene Proteins B-rafTumor EscapeReis e SousaSahaiCBDevelopmental Biology06 Biological Sciences11 Medical and Health Sciences