[1,2-BIS(2-HYDROXYPHENYL)ETHYLENEDIAMINE]DICHLOROPLATINUM(II), A NEW COMPOUND FOR THE THERAPY OF OVARIAN-CANCER .3. DETAILED EVALUATION OF THE ANTITUMOR-ACTIVITY OF THE ENANTIOMERIC COMPLEXES ON THE HUMAN NIH-OVCAR-3 OVARIAN-CANCER CELL-LINE

被引:4
作者
BERNHARDT, G [1 ]
GUST, R [1 ]
REILE, H [1 ]
VOMORDE, HD [1 ]
MULLER, R [1 ]
KELLER, C [1 ]
SPRUSS, T [1 ]
SCHONENBERGER, H [1 ]
BURGEMEISTER, T [1 ]
MANNSCHRECK, A [1 ]
RANGE, KJ [1 ]
KLEMENT, U [1 ]
机构
[1] UNIV REGENSBURG,INST ORGAN CHEM,SONDERFORSCHUNGSBEREICH 234,W-8400 REGENSBURG,GERMANY
关键词
STEREOISOMERIC [1,2-BIS(2-HYDROXYPHENYL)ETHYLENEDIAMINE]DICHLOROPLATINUM(II); EVALUATION ON NIH-OVCAR-3 OVARIAN CANCER CELL LINE; COMBINATION WITH BUTHIONINE SULFOXIMINE;
D O I
10.1007/BF01410136
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The stereoisomeric [1,2-bis(2-hydroxyphenyl) ethylenediamine]dichloroplatinum(II) complexes were thoroughly tested on the cisplatin-resistant human NIH: OVCAR-3 ovarian cancer cell line. The racemate and its enantiomers produced cytocidal effects at a concentration of 2.5-mu-M (incubation time 256 h). The meso form, however, was merely cytostatically active. Differences between the enantiomers became evident after a short drug incubation time (1 h) followed by an incubation in drug-free medium (243 h). The S,S-configurated enantiomer (-)-3-PtCl2 proved to be the most active compound. To achieve cytocidal effects concentrations of 2.5-5.0-mu-M and incubation times of about 3 h were necessary for (-)-3-PtCl2. This compound is also sufficiently stable under test conditions as shown by the preincubation in cell-free medium for 3 h. These results and the augmentation of its antitumor activity by buthionine sulfoximine recommend the further preclinical development of (-)-3-PtCl2 for clinical use.
引用
收藏
页码:209 / 215
页数:7
相关论文
共 23 条
[1]   [1,2-BIS(2-HYDROXYPHENYL)ETHYLENEDIAMINE]DICHLOROPLATINUM(II), A NEW COMPOUND FOR THE THERAPY OF OVARIAN-CANCER .2. SYNTHESIS AND PRELIMINARY TESTING OF THE ENANTIOMERIC COMPLEXES [J].
BERNHARDT, G ;
GUST, R ;
REILE, H ;
VOMORDE, HD ;
MULLER, R ;
KELLER, C ;
SPRUSS, T ;
SCHONENBERGER, H ;
BURGEMEISTER, T ;
MANNSCHRECK, A ;
RANGE, KJ ;
KLEMENT, U .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1992, 118 (03) :201-208
[2]   STANDARDIZED KINETIC MICROASSAY TO QUANTIFY DIFFERENTIAL CHEMOSENSITIVITY ON THE BASIS OF PROLIFERATIVE ACTIVITY [J].
BERNHARDT, G ;
REILE, H ;
BIRNBOCK, H ;
SPRUSS, T ;
SCHOENENBERGER, H .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1992, 118 (01) :35-43
[3]  
GRIFFITH OW, 1979, J BIOL CHEM, V254, P7558
[4]   COMPLEXES OF PLATINUM(II) WITH CHIRAL DIAMINES AND GUANOSINE - STEREOCHEMICAL INVESTIGATION RELATED TO THE MECHANISM OF THE ANTI-TUMOR ACTIVITY OF CIS-BIS(AMINE)PLATINUM(II) TYPE COMPLEXES [J].
GULLOTTI, M ;
PACCHIONI, G ;
PASINI, A ;
UGO, R .
INORGANIC CHEMISTRY, 1982, 21 (05) :2006-2014
[5]   ENANTIOMERIC CISPLATIN ANALOGS - AN INVESTIGATION ON THEIR ACTIVITY TOWARDS TUMORS IN MICE [J].
GULLOTTI, M ;
PASINI, A ;
UGO, R .
INORGANICA CHIMICA ACTA-BIOINORGANIC CHEMISTRY, 1984, 91 (03) :223-227
[6]   AQUA[1-(2,6-DICHLORO-4-HYDROXYPHENYL)-2-PHENYLETHYLENEDIAMINE](SULFATO)PLATINUM-(II) COMPLEXES WITH VARIABLE SUBSTITUENTS IN THE 2-PHENYL RING .1. SYNTHESIS AND ANTITUMOR AND ESTROGENIC PROPERTIES [J].
GUST, R ;
BURGEMEISTER, T ;
MANNSCHRECK, A ;
SCHONENBERGER, H .
JOURNAL OF MEDICINAL CHEMISTRY, 1990, 33 (09) :2535-2544
[7]  
HAMILTON TC, 1983, CANCER RES, V43, P5379
[8]   INHIBITORY EFFECTS OF ANTI-TUMOR PLATINUM COMPOUNDS ON DNA, RNA AND PROTEIN SYNTHESES IN MAMMALIAN CELLS IN-VITRO [J].
HARDER, HC ;
ROSENBERG, B .
INTERNATIONAL JOURNAL OF CANCER, 1970, 6 (02) :207-+
[9]   THE SEED STOCK CONCEPT AND QUALITY-CONTROL FOR CELL-LINES [J].
HAY, RJ .
ANALYTICAL BIOCHEMISTRY, 1988, 171 (02) :225-237
[10]   CIS-DICHLORODIAMMINEPLATINUM (II) - PERSISTENT AND SELECTIVE INHIBITION OF DEOXYRIBONUCLEIC ACID SYNTHESIS IN-VIVO [J].
HOWLE, JA ;
GALE, GR .
BIOCHEMICAL PHARMACOLOGY, 1970, 19 (10) :2757-&