The role of prostanoids in regulatory T cells and their implications in inflammatory diseases and cancers

dc.contributor.authorPrasongtanakij S.
dc.contributor.authorSoontrapa K.
dc.contributor.authorThumkeo D.
dc.contributor.correspondencePrasongtanakij S.
dc.contributor.otherMahidol University
dc.date.accessioned2025-04-10T18:04:24Z
dc.date.available2025-04-10T18:04:24Z
dc.date.issued2025-06-01
dc.description.abstractRegulatory T cells (Tregs) play an important role in the immune system through the regulation of immunological self-tolerance and homeostasis. Furthermore, increasing evidence suggests the potential contribution of Tregs beyond immunity in the process of repairing various injured tissues. Tregs are generally characterised by the constitutive expression of forkhead box protein 3 (FOXP3) transcription factor in the nucleus and high expression levels of CD25 and CTLA-4 on the cell surface. To date, a large number of molecules have been identified as key regulators of Treg differentiation and function. Among these molecules are prostanoids, which are multifaceted lipid mediators. Prostanoids are produced from arachidonic acid through the catalytic activity of the enzyme cyclooxygenase and exert their functions through the 9 cognate receptors, DP1‐2, EP1-EP4, FP, IP and TP. We briefly review previous studies on the regulatory mechanism of Tregs and then discuss recent works on the modulatory role of prostanoids.
dc.identifier.citationEuropean Journal of Cell Biology Vol.104 No.2 (2025)
dc.identifier.doi10.1016/j.ejcb.2025.151482
dc.identifier.eissn16181298
dc.identifier.issn01719335
dc.identifier.scopus2-s2.0-105001543951
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/109452
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.subjectMedicine
dc.titleThe role of prostanoids in regulatory T cells and their implications in inflammatory diseases and cancers
dc.typeReview
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105001543951&origin=inward
oaire.citation.issue2
oaire.citation.titleEuropean Journal of Cell Biology
oaire.citation.volume104
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationGraduate School of Medicine
oairecerif.author.affiliationKyoto University Faculty of Medicine

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