ZR-75-1 human breast cancer cells: expression of inducible nitric oxide synthase and effect of tamoxifen and phorbol ester on nitric oxide production

被引:24
作者
Alalami, O [1 ]
Martin, JHJ [1 ]
机构
[1] Wolverhampton Univ, Sch Hlth Sci, Div Biomed Sci, Wolverhampton WV1 1DJ, England
关键词
breast cancer; nitric oxide synthase; tamoxifen; phorbol ester;
D O I
10.1016/S0304-3835(97)00404-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The existence of the L-arginine-nitric oxide pathway was investigated in ZR-75-1 human breast cancer cells. The presence of inducible nitric oxide synthase in these cells was confirmed by staining with an anti-iNOS antibody. ZR-75-1 cells spontaneously produced nitric oxide (NO) and this production could be significantly (P < 0.001) enhanced by L-arginine (0.01-10 mM) and was inhibited by L-NAME (2 mM). Stimulating the cells with phorbol 12-myristate 13-acetate (PMA) (200-1000 nM) resulted in a significant (P < 0.001) increase in NO; secreted into the medium. Although treatment of the same cells with tamoxifen (10-(10)-10(-6) M) had no effect on NO production, tamoxifen was able to significantly (P < 0.001) downregulate PMA-enhanced nitrite production. Our results suggest that tamoxifen could play a role in the biology of nitric oxide in breast tumours. (C) 1998 Elsevier Science Ireland Ltd.
引用
收藏
页码:99 / 105
页数:7
相关论文
共 28 条
[1]   INHIBITORS OF NITRIC-OXIDE SYNTHASE SELECTIVELY REDUCE FLOW IN TUMOR-ASSOCIATED NEOVASCULATURE [J].
ANDRADE, SP ;
HART, IR ;
PIPER, PJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1992, 107 (04) :1092-1095
[2]  
BANI D, 1995, CANCER RES, V55, P5272
[3]   NITRIC-OXIDE - A PHYSIOLOGICAL MESSENGER MOLECULE [J].
BREDT, DS ;
SNYDER, SH .
ANNUAL REVIEW OF BIOCHEMISTRY, 1994, 63 :175-195
[4]   Inflammatory mediators stimulate arginine transport and arginine-derived nitric oxide production in a murine breast cancer cell line [J].
Cendan, JC ;
Topping, DL ;
Pruitt, J ;
Snowdy, S ;
Copeland, EM ;
Lind, DS .
JOURNAL OF SURGICAL RESEARCH, 1996, 60 (02) :284-288
[5]  
DONG ZY, 1994, CANCER RES, V54, P789
[6]   MURINE CYTOTOXIC ACTIVATED MACROPHAGES INHIBIT ACONITASE IN TUMOR-CELLS - INHIBITION INVOLVES THE IRON-SULFUR PROSTHETIC GROUP AND IS REVERSIBLE [J].
DRAPIER, JC ;
HIBBS, JB .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 78 (03) :790-797
[7]  
ENGEL LW, 1978, CANCER RES, V38, P3352
[8]   ISOFORMS OF NITRIC-OXIDE SYNTHASE - PROPERTIES, CELLULAR-DISTRIBUTION AND EXPRESSIONAL CONTROL [J].
FORSTERMANN, U ;
GATH, I ;
SCHWARZ, P ;
CLOSS, EI ;
KLEINERT, H .
BIOCHEMICAL PHARMACOLOGY, 1995, 50 (09) :1321-1332
[9]   ANALYSIS OF NITRATE, NITRITE, AND [N-15]-LABELED NITRATE IN BIOLOGICAL-FLUIDS [J].
GREEN, LC ;
WAGNER, DA ;
GLOGOWSKI, J ;
SKIPPER, PL ;
WISHNOK, JS ;
TANNENBAUM, SR .
ANALYTICAL BIOCHEMISTRY, 1982, 126 (01) :131-138
[10]   INHIBITION OF PROTEIN-KINASE-C MEDIATED SIGNAL TRANSDUCTION BY TAMOXIFEN - IMPORTANCE FOR ANTITUMOR-ACTIVITY [J].
HORGAN, K ;
COOKE, E ;
HALLETT, MB ;
MANSEL, RE .
BIOCHEMICAL PHARMACOLOGY, 1986, 35 (24) :4463-4465