Combinatorial effects of nonsteroidal anti-inflammatory drugs and food constituents on production of prostaglandin E2 and tumor necrosis factor-α in RAW264.7 murine macrophages

被引:32
作者
Murakami, A [1 ]
Takahashi, D
Hagihara, K
Koshimizu, K
Ohigashi, H
机构
[1] Kyoto Univ, Grad Sch Agr, Div Food Sci & Biotechnol, Kyoto 6068502, Japan
[2] Kinki Univ, Fac Biol Oriented Sci & Technol, Dept Biotechnol Sci, Wakayama 6496493, Japan
关键词
epigallocatechin gallate; genistein; cyclooxygenase; RAW264.7; cells; inflammation;
D O I
10.1271/bbb.67.1056
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
Combinatorial chemopreventive strategies, in contrast to those with individual agents, show potential in terms of potentially lower toxicity and higher efficacy. In this study, we combined several agents and examined their suppressive effects on the combined lipopolysaccharide (LPS)- and interferon(IFN)-gamma-induced formation of proinflammatory mediators, including prostaglandin (PG) E-2 and tumor necrosis factor (TNF)-alpha, in RAW264.7 murine macrophages. The combinatorial effects of indomethacin/genistein (GEN) and aspirin/GEN were found to be synergistic for PGE(2) suppression, while the nimesulide/GEN combination was antagonistic. Further, while (-)-epigallocatechin gallate (EGCG) alone increased LPS/IFM-gamma-induced production of PGE(2) and TNF-alpha as well as cyclooxygenase-2 expression, the EGCG/GEN combination markedly suppressed these parameters. Our results suggest that certain chemopreventive agents act complexly and that, when used in combination, they affect the intracellular signaling pathways of the paired agents to exert additive, synergistic, or antagonistic effects.
引用
收藏
页码:1056 / 1062
页数:7
相关论文
共 37 条
[1]  
Brenner DE, 2000, J CELL BIOCHEM, P121
[2]   Difluoromethylornithine in combination with tamoxifen in female rats: 13-week oral toxicity study [J].
Brown, AP ;
Morrissey, RL ;
Crowell, JA ;
Levine, BS .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1999, 44 (06) :475-483
[3]   Tyrosine kinase inhibitors prevent cytokine-induced expression of iNOS and COX-2 by human islets [J].
Corbett, JA ;
Kwon, G ;
Marino, MH ;
Rodi, CP ;
Sullivan, PM ;
Turk, J ;
McDaniel, ML .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 270 (06) :C1581-C1587
[4]   Molecular alterations in gastric cancer:: the role of Helicobacter pylori [J].
Ebert, MPA ;
Yu, J ;
Sung, JJ ;
Malfertheiner, P .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2000, 12 (07) :795-798
[5]  
Fujiki H, 2000, CANCER DETECT PREV, V24, P91
[6]   Chemoprevention of N-nitroso-N-methylurea-induced rat mammary cancer by miso and tamoxifen, alone and in combination [J].
Gotoh, T ;
Yamada, K ;
Ito, A ;
Yin, H ;
Kataoka, T ;
Dohi, K .
JAPANESE JOURNAL OF CANCER RESEARCH, 1998, 89 (05) :487-495
[7]   Effects of purified green and black tea polyphenols on cyclooxygenase and lipoxygenase-dependent metabolism of arachidonic acid in human colon mucosa and colon tumor tissues [J].
Hong, JG ;
Smith, TJ ;
Ho, CT ;
August, DA ;
Yang, CS .
BIOCHEMICAL PHARMACOLOGY, 2001, 62 (09) :1175-1183
[8]  
Jacoby RF, 2000, CANCER RES, V60, P1864
[9]   Tumor necrosis factor-α induces the expression of DR6, a member of the TNF receptor family, through activation of NF-κB [J].
Kasof, GM ;
Lu, JJ ;
Liu, DR ;
Speer, B ;
Mongan, KN ;
Gomes, BC ;
Lorenzi, MV .
ONCOGENE, 2001, 20 (55) :7965-7975
[10]   Molecular mechanism of viral hepatocarcinogenesis [J].
Koike, K ;
Tsutsumi, T ;
Fujie, H ;
Shintani, Y ;
Moriya, K .
ONCOLOGY, 2002, 62 :29-37