New insights into the role of COX 2 in inflammation

被引:103
作者
Gilroy, DW
Colville-Nash, PR
机构
[1] Univ Texas, Houston Med Sch, Vasc Biol Res Ctr, Houston, TX 77030 USA
[2] Univ Texas, Houston Med Sch, Div Hematol, Houston, TX 77030 USA
[3] Univ London St Bartholomews Hosp Med Coll, Dept Expt Pathol, London EC1M 6BQ, England
[4] Royal London Sch Med & Dent, London EC1M 6BQ, England
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2000年 / 78卷 / 03期
关键词
cyclo-oxygenase; nonsteroidal anti-inflammatory drugs; inflammation; peroxisome proliferator-activated receptor; cyclopentenone prostaglandins; stress proteins;
D O I
10.1007/s001090000094
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cyclo-oxygenase (COX) is responsible for the synthesis of bioactive prostanoids, the inhibition of which serves as the basis for the mode of action of clinically used nonsteroidal anti-inflammatory drugs. While there were suggestions as early as the 1970s that an inducible isoform of COX exists, it was only in the early 1990s that COX 2 was identified, cloned and sequenced. Not surprisingly, this new isoform was expressed at sites of inflammation and reported to contribute to the inflammatory response. Recently, however, evidence is emerging to suggest that COX 2 also has anti-inflammatory properties. In this review, the two faces of COX 2 are examined, with emphasis on its role in regulating inflammatory resolution, including possible mechanisms of action.
引用
收藏
页码:121 / 129
页数:9
相关论文
共 88 条
[11]   ANGIOGENESIS AND RHEUMATOID-ARTHRITIS - PATHOGENIC AND THERAPEUTIC IMPLICATIONS [J].
COLVILLENASH, PR ;
SCOTT, DL .
ANNALS OF THE RHEUMATIC DISEASES, 1992, 51 (07) :919-925
[12]   Inhibition of poliovirus replication by prostaglandins A and J human cells [J].
Conti, C ;
Mastromarino, P ;
Tomao, P ;
DeMarco, A ;
Pica, F ;
Santoro, MG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (02) :367-372
[13]   The PPAR alpha-leukotriene B-4 pathway to inflammation control [J].
Devchand, PR ;
Keller, H ;
Peters, JM ;
Vazquez, M ;
Gonzalez, FJ ;
Wahli, W .
NATURE, 1996, 384 (6604) :39-43
[14]   RENAL ABNORMALITIES AND AN ALTERED INFLAMMATORY RESPONSE IN MICE LACKING CYCLOOXYGENASE-II [J].
DINCHUK, JE ;
CAR, BD ;
FOCHT, RJ ;
JOHNSTON, JJ ;
JAFFEE, BD ;
COVINGTON, MB ;
CONTEL, NR ;
ENG, VM ;
COLLINS, RJ ;
CZERNIAK, PM ;
GORRY, SA ;
TRZASKOS, JM .
NATURE, 1995, 378 (6555) :406-409
[15]   Induction of ferritin and heat shock proteins by prostaglandin A1 in human monocytes -: Evidence for transcriptional and post-transcriptional regulation [J].
Elia, G ;
Polla, B ;
Rossi, A ;
Santoro, MG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 264 (03) :736-745
[16]   The organization, promoter analysis, and expression of the human PPAR gamma gene [J].
Fajas, L ;
Auboeuf, D ;
Raspe, E ;
Schoonjans, K ;
Lefebvre, AM ;
Saladin, R ;
Najib, J ;
Laville, M ;
Fruchart, JC ;
Deeb, S ;
VidalPuig, A ;
Flier, J ;
Briggs, MR ;
Staels, B ;
Vidal, H ;
Auwerx, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (30) :18779-18789
[17]   15-DEOXY-DELTA(12,14)-PROSTAGLANDIN J(2) IS A LIGAND FOR THE ADIPOCYTE DETERMINATION FACTOR PPAR-GAMMA [J].
FORMAN, BM ;
TONTONOZ, P ;
CHEN, J ;
BRUN, RP ;
SPIEGELMAN, BM ;
EVANS, RM .
CELL, 1995, 83 (05) :803-812
[18]   Peroxisome proliferator-activated receptor-alpha activators regulate genes governing lipoprotein metabolism, vascular inflammation and atherosclerosis [J].
Fruchart, JC ;
Duriez, P ;
Staels, B .
CURRENT OPINION IN LIPIDOLOGY, 1999, 10 (03) :245-257
[19]   NS-398, A NEW ANTIINFLAMMATORY AGENT, SELECTIVELY INHIBITS PROSTAGLANDIN-G/H SYNTHASE CYCLOOXYGENASE (COX-2) ACTIVITY IN-VITRO [J].
FUTAKI, N ;
TAKAHASHI, S ;
YOKOYAMA, M ;
ARAI, I ;
HIGUCHI, S ;
OTOMO, S .
PROSTAGLANDINS, 1994, 47 (01) :55-59
[20]   NS-398, A NOVEL NONSTEROIDAL ANTIINFLAMMATORY DRUG WITH POTENT ANALGESIC AND ANTIPYRETIC EFFECTS, WHICH CAUSES MINIMAL STOMACH LESIONS [J].
FUTAKI, N ;
YOSHIKAWA, K ;
HAMASAKA, Y ;
ARAI, I ;
HIGUCHI, S ;
IIZUKA, H ;
OTOMO, S .
GENERAL PHARMACOLOGY, 1993, 24 (01) :105-110