Non platinum metal complexes as anti-cancer drugs

被引:564
作者
Ott, Ingo [1 ]
Gust, Ronald [1 ]
机构
[1] Free Univ Berlin, Inst Pharm, D-1000 Berlin, Germany
关键词
anti-tumour; cobalt; gold; metal complexes; ruthenium;
D O I
10.1002/ardp.200600151
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The development of metal complexes with platinum central atoms such as cisplatin or carboplatin had an enormous impact on current cancer chemotherapy. However, the spectrum of cancers that can be treated with platinum agents is narrow and treatment efficacy suffers from side effects and resistance phenomena. These unresolved problems in platinum-based anti-cancer therapy have stimulated increased research efforts in the search for novel non platinum-containing metal species as cytostatic agents. Preclinical and clinical investigations showed that the development of new metal agents with modes of action different from cisplatin is possible. Thus, complexes with iron, cobalt, or gold central atoms have shown promising results in preclinical studies and compounds with titanium, ruthenium, or gallium central atoms have already been evaluated in phase I and phase II trials. This review covers some relevant examples of preclinical and clinical research on novel non platinum metal complexes.
引用
收藏
页码:117 / 126
页数:10
相关论文
共 131 条
[1]   Radiolytic and cellular reduction of a novel hypoxia-activated cobalt(III) prodrug of a chloromethylbenzindoline DNA minor groove alkylator [J].
Ahn, G-One ;
Botting, K. Jane ;
Patterson, Adam V. ;
Ware, David C. ;
Tercel, Moana ;
Wilson, William R. .
BIOCHEMICAL PHARMACOLOGY, 2006, 71 (12) :1683-1694
[2]   Optimization of the auxiliary ligand shell of cobalt(III)(8-hydroxyquinoline) complexes as model hypoxia-selective radiation-activated prodrugs [J].
Ahn, GO ;
Ware, DC ;
Denny, WA ;
Wilson, WR .
RADIATION RESEARCH, 2004, 162 (03) :315-325
[3]   Ruthenium antimetastatic agents [J].
Alessio, E ;
Mestroni, G ;
Bergamo, A ;
Sava, G .
CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2004, 4 (15) :1525-1535
[4]  
Alessio E, 2004, MET IONS BIOL SYST, V42, P323
[5]   Development of organometallic (organo-transition metal) pharmaceuticals [J].
Allardyce, CS ;
Dorcier, A ;
Scolaro, C ;
Dyson, PJ .
APPLIED ORGANOMETALLIC CHEMISTRY, 2005, 19 (01) :1-10
[6]   INVIVO INHIBITION OF TUMOR-GROWTH BY RUTHENIUM RED - ITS RELATIONSHIP WITH METABOLISM OF CALCIUM IN TUMOR [J].
ANGHILERI, LJ .
ZEITSCHRIFT FUR KREBSFORSCHUNG UND KLINISCHE ONKOLOGIE, 1975, 83 (03) :213-217
[7]  
[Anonymous], COORD CHEM REV
[8]   Thioredoxin reductase as a pathophysiological factor and drug target [J].
Becker, K ;
Gromer, S ;
Schirmer, RH ;
Müller, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (20) :6118-6125
[9]  
Bergamo A, 2002, INT J ONCOL, V21, P1331
[10]  
BERNERSPRICE SJ, 1986, CANCER RES, V46, P5486