The cyclooxygenase (COX) signaling pathway is frequently dysregulated in cancer, resulting in aberrant production of prostaglandins - a distinct class of bioactive lipids with immunoregulatory functions. One of these factors, prostaglandin E2 (PGE₂), has over the years emerged as one of the predominant COX-derived factors in tumors, with numerous studies exploring its downstream signaling and functional impact across diverse cell types. Recent studies have substantially advanced our understanding of how PGE2 promotes cancer immune evasion through its deleterious effects on tumor-infiltrating immune cells. Here, we summarize some key principles of PGE2-mediated immune regulation in tumors, focusing on current knowledge of PGE2 production mechanisms and recent advances in our understanding of molecular features and functional consequences of PGE2-signaling in tumor-infiltrating immune cells. We further discuss how strategies aimed at disrupting the local activity of prostaglandins in tumors, or interfering with the distinct molecular features characteristic for PGE2 signaling in immune cells, may provide attractive new avenues for cancer therapy.
No takes yet. Share an insight, caveat, or question.
Müller et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: