Prostaglandin E2 production in ovarian cancer cell lines is regulated by cyclooxygenase-1, not cyclooxygenase-2

被引:35
作者
Kino, Y
Kojima, F
Kiguchi, K
Igarashi, R
Ishizuka, B
Kawai, S
机构
[1] Toho Univ, Sch Med, Dept Internal Med,Div Rheumatol, Ota Ku, Tokyo 1438541, Japan
[2] St Marianna Univ, Sch Med, Inst Med Sci, Miyamae Ku, Kawasaki, Kanagawa 2168512, Japan
[3] St Marianna Univ, Sch Med, Dept Obstet & Gynecol, Miyamae Ku, Kawasaki, Kanagawa 2168512, Japan
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 2005年 / 73卷 / 02期
关键词
D O I
10.1016/j.plefa.2005.04.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The significance of cyclooxygenase-2 (COX-2) expression in ovarian cancer has been discussed. In this study, we found increased expression of COX-1 mRNA and protein in three out of 10 ovarian cancer cell lines. Prostaglandin E-2 (PGE(2)) production was elevated in these three cell lines, but not in other seven cell lines. COX-2 protein was not detected in any of the cell lines. Cytosolic prostaglandin E synthase (cPGES) mRNA and protein were detected in all 10 cell lines. Membrane-associated PGES-1 (mPGES-1) was detected in some of the ovarian cell lines, but its presence did not correspond with PGE(2) production. In contrast, mPGES-2 mRNA and protein were detected in all 10 cell lines. A nonselective COX inhibitor (indometacin) and a selective COX-1 inhibitor (SC-560) strongly inhibited PGE(2) production by the three cell lines, while selective COX-2 inhibitors (NS-398 and rofecoxib) did not inhibit PGE(2) production. In addition, increased expression of COX-1, not COX-2 protein was observed in the mass of ovarian cancer tissues from 22 patients when compared with that in normal tissue. These findings suggest that COX-1 might be a major enzyme regulating PGE(2) production in ovarian cancer cells. (C) 2005 Elsevier Ltd. All rights reserved.
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页码:103 / 111
页数:9
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