Volume 12, Issue 12 p. 1063-1073
Review
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Cyclooxygenase in biology and disease

Raymond N. DuBois

Corresponding Author

Raymond N. DuBois

Departments of Medicine/GI & Cell Biology, Vanderbilt University Medical Center, Nashvillew, Tennessee, 37232 USA

Correspondence: Department of Medicine/GI; MCN C-2104, Vanderbilt University Medical Center, Nashville, TN 37232-2279, USA. E-mail: [email protected]Search for more papers by this author
Steven B. Abramson

Steven B. Abramson

Department of Rheumatology, New York University School of Medicine, Hospital for Joint Diseases, New York, New York, 10003 USA

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Leslie Crofford

Leslie Crofford

Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 48109-0680

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Rajnish A. Gupta

Rajnish A. Gupta

Departments of Medicine/GI & Cell Biology, Vanderbilt University Medical Center, Nashvillew, Tennessee, 37232 USA

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Lee S. Simon

Lee S. Simon

Division of Rheumatology, Harvard Medical School, Beth Israel Deaconness Medical Center, Boston, Massachusetts, 02215 USA

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Leo B. A. van de Putte

Leo B. A. van de Putte

Division of Rheumatology, University Hospital Nijmegen, 6500, HB, Nijmegen, The Netherlands

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Peter E. Lipsky

Peter E. Lipsky

Rheumatic Diseases Division, Harold C. Simmons Arthritis Research Center, The University of Texas Southwestern Medical Center at Dallas, Texas, 75235-8884 USA

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First published: 01 September 1998
Citations: 1,778

ABSTRACT

Cyclooxygenase (COX), the key enzyme required for the conversion of arachidonic acid to prostaglandins was first identified over 20 years ago. Drugs, like aspirin, that inhibit cyclooxygenase activity have been available to the public for about 100 years. In the past decade, however, more progress has been made in understanding the role of cyclooxygenase enzymes in biology and disease than at any other time in history. Two cyclooxygenase isoforms have been identified and are referred to as COX-1 and COX-2. Under many circumstances the COX-1 enzyme is produced constitutively (i.e., gastric mucosa) whereas COX-2 is inducible (i.e., sites of inflammation). Here, we summarize the current understanding of the role of cyclooxygenase-1 and -2 in different physiological situations and disease processes ranging from inflammation to cancer. We have attempted to include all of the most relevant material in the field, but due to the rapid progress in this area of research we apologize that certain recent findings may have been left out.—DuBois, R. N., Abramson, S. B., Crofford, L., Gupta, R. A., Simon, L. S., van de Putte, L. B. A., Lipsky, P. E. Cyclooxygenase in biology and disease. FASEB J. 12, 1063–1073 (1998)