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pubmed-article:15155382pubmed:abstractTextInducible cyclooxygenase (COX-2) catalyzes the first step in prostanoid biosynthesis and is considered a proinflammatory enzyme. COX-2 and type 1 inducible PGE synthase (mPGES-1) have a role in metalloproteinase (MMP) release leading to plaque rupture. In contrast, lipocalin-type PGD synthase (L-PGDS) has been shown to exert antiinflammatory actions. Thus, in this study we investigated whether a shift from a PGDS-oriented to a PGES-oriented profile in arachidonate metabolism leads to inflammatory activation in rupture-prone plaque macrophages.lld:pubmed
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pubmed-article:15155382pubmed:articleTitleBalance between PGD synthase and PGE synthase is a major determinant of atherosclerotic plaque instability in humans.lld:pubmed
pubmed-article:15155382pubmed:affiliationAtherosclerosis Prevention Center, University of Chieti G D'Annunzio, School of Medicine, Chieti, Italy. fcipollone@unich.itlld:pubmed
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