Activity of [1,2-di(cyclopentadienyl)-1,2-di(p-N,N-domethylaminophenyl)-ethanediyl] titanium dichloride against tumor colony-forming units

被引:49
|
作者
Oberschmidt, O
Hanauske, AR
Rehmann, FJK
Strohfeldt, K
Sweeney, N
Tacke, M
机构
[1] Allgemeines Krankenhaus St Georg, D-20099 Hamburg, Germany
[2] Univ Coll Dublin, Ctr Synth & Chem Biol, Dept Chem, Conway Inst Biomol & Biomed Res, Dublin 2, Ireland
关键词
anti-cancer drug; titanocene dichloride; clonogenic growth; human tumors;
D O I
10.1097/00001813-200511000-00005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
[1,2-di(cyclopentadienyl)-1,2-di(p-N,N-dimethylamino-phenyl)-ethanediyl] titanium dichloride is a newly synthesized transition metal-based anti-cancer drug. We studied the anti-tumor activity of this drug (final concentrations: 25, 250 and 2500 mu mol/l) against freshly explanted human tumors, using an in vitro soft agar cloning system. A total of eight tumor samples were evaluated using 1-h exposures. Additionally, the breast carcinoma cell line MCF-7 was examined with regard to sensitivity. The tested compound was markedly active against one renal cancer sample, whereas other renal tumors were resistant. Concentration-dependent anti-tumor activity was demonstrated for all samples except for melanoma. At concentrations of 250 mu mol/l or less, the compound was less active than cisplatin or equally active at 0.2 mu g/ml, whereas at 2500 mu mol/l it showed a significant cytotoxic activity against a wide spectrum of tumor types. The highest activity was observed against renal carcinomas (three of three tumor specimens inhibited at 2500 mu mol/l). Sensitivity was also highly remarkable in the breast cancer cell line MCF-7 inhibited in a range of 25-2500 mu mol/l, whereas melanoma cells seemed to be profoundly resistant. Further clinical development of this drug appears warranted because of the broad cytotoxic activity shown.
引用
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页码:1071 / 1073
页数:3
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