Prostaglandin receptors are mediators of vascular function in endometrial pathologies

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This paper reviews evidence that prostaglandin receptors mediate vascular function in endometrial pathologies by promoting angiogenesis and influencing tissue phenotypes.

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Abstract

Prostaglandins are bioactive lipids produced from arachidonic acid by cyclooxygenase enzymes and specific terminal prostanoid synthase enzymes. Following biosynthesis, prostaglandins exert an autocrine/paracrine function by coupling to specific prostanoid G protein-coupled receptors to activate intracellular signaling and gene transcription. For many years prostaglandins have been recognised as key molecules in reproductive biology by regulating ovulation, endometrial physiology and proliferation of endometrial glands and menstruation. More recently a role for COX enzymes and prostaglandins has been ascertained in reproductive tract pathology, including dysmenorrhea, endometriosis, menorrhagia and cancer. Emerging evidence supports a role for COX enzymes, prostaglandins and prostaglandin receptor signaling pathways in a multitude of phenotypic changes in reproductive tissues including the promotion of angiogenesis and vascular function. Here we provide an overview of some of the findings from these studies with specific emphasis on the role of cyclooxygenase enzymes, prostaglandins and their receptors in benign and neoplastic pathologies of the human endometrium.

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Condition tags

dysmenorrheaendometriosis

MeSH descriptors

Blood Vessels Endometrium Endometrium Neovascularization, Physiologic Receptors, Prostaglandin Animals Blood Vessels Dysmenorrhea Dysmenorrhea Electron Transport Complex IV Electron Transport Complex IV Endometrial Neoplasms Endometrial Neoplasms Endometriosis Endometriosis Endometrium Female Humans Menorrhagia Menorrhagia

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Source provenance

europepmc
last seen: 2026-08-22T06:09:51.966504+00:00
pubmed
last seen: 2026-05-13T22:15:18.313808+00:00
unpaywall
last seen: 2026-08-22T06:23:50.750314+00:00
License: public-domain-us · commercial use OK · attribution required
Courtesy of the U.S. National Library of Medicine