Cyclooxygenases: structural, cellular, and molecular biology.

Article Details

Citation

Smith WL, DeWitt DL, Garavito RM

Cyclooxygenases: structural, cellular, and molecular biology.

Annu Rev Biochem. 2000;69:145-82.

PubMed ID
10966456 [ View in PubMed
]
Abstract

The prostaglandin endoperoxide H synthases-1 and 2 (PGHS-1 and PGHS-2; also cyclooxygenases-1 and 2, COX-1 and COX-2) catalyze the committed step in prostaglandin synthesis. PGHS-1 and 2 are of particular interest because they are the major targets of nonsteroidal anti-inflammatory drugs (NSAIDs) including aspirin, ibuprofen, and the new COX-2 inhibitors. Inhibition of the PGHSs with NSAIDs acutely reduces inflammation, pain, and fever, and long-term use of these drugs reduces fatal thrombotic events, as well as the development of colon cancer and Alzheimer's disease. In this review, we examine how the structures of these enzymes relate mechanistically to cyclooxygenase and peroxidase catalysis, and how differences in the structure of PGHS-2 confer on this isozyme differential sensitivity to COX-2 inhibitors. We further examine the evidence for independent signaling by PGHS-1 and PGHS-2, and the complex mechanisms for regulation of PGHS-2 gene expression.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Prostaglandin G/H synthase 1P23219Details
Prostaglandin G/H synthase 2P35354Details