Natarajan G, Malathi R, Holler E
Department of Genetics, Dr. Alm Post Graduate Institute of Basic Medical Sciences, University of Madras, India.
Biochem Pharmacol. 1999 Nov 15;58(10):1625-9. doi: 10.1016/s0006-2952(99)00250-6.
The molecular mechanism of carboplatin [cis-1,1-cyclobutanedicarboxylatodiammineplatinum(II)] activation is still unresolved. We studied the binding of carboplatin to calf thymus DNA in the presence of thiourea, glutathione, and human breast cancer MCF-7 cell cytoplasmic extracts by measurement of DNA-dependent ethidium bromide fluorescence and atomic absorption spectroscopy. After a 96-hr period of reaction, the decrease in the DNA-dependent fluorescence yield of ethidium bromide due to the formation of platinum (Pt)-DNA adducts increased significantly in the presence of thiourea (6-fold) and glutathione (3- to 4-fold) as compared to the controls in the absence of the nucleophiles. There was also a marked elevation in the levels of platinum incorporated into DNA, measured by atomic absorption spectroscopy (2- to 3-fold and 5- to 7-fold for thiourea and glutathione, respectively). More remarkably, the Pt-DNA adducts formed in the presence of cytoplasmic extracts of MCF-7 human breast cancer cells also showed similar results in a dose-related fashion. Carboplatin, therefore, displayed a characteristic increase in DNA binding/damaging in the presence of the very same S-containing nucleophiles that showed the expected quenching effects in the case of cisplatin [cis-diamminedichloroplatinum (II)]. We propose a nucleophile-facilitated release of the active species of carboplatin prior to binding with DNA.
卡铂[顺式-1,1-环丁烷二羧酸二氨合铂(II)]的激活分子机制仍未得到解决。我们通过测量DNA依赖性溴化乙锭荧光和原子吸收光谱,研究了在硫脲、谷胱甘肽和人乳腺癌MCF-7细胞质提取物存在的情况下,卡铂与小牛胸腺DNA的结合情况。反应96小时后,与不存在亲核试剂的对照组相比,在硫脲(6倍)和谷胱甘肽(3至4倍)存在的情况下,由于铂(Pt)-DNA加合物的形成而导致的溴化乙锭DNA依赖性荧光产率的降低显著增加。通过原子吸收光谱法测量,掺入DNA中的铂水平也有显著升高(硫脲和谷胱甘肽分别为2至3倍和5至7倍)。更值得注意的是,在MCF-7人乳腺癌细胞的细胞质提取物存在的情况下形成的Pt-DNA加合物也以剂量相关的方式显示出类似的结果。因此,卡铂在存在相同的含硫亲核试剂时,其与DNA的结合/损伤表现出特征性增加,而这些亲核试剂在顺铂[顺式二氯二氨合铂(II)]的情况下显示出预期的猝灭效应。我们提出在卡铂与DNA结合之前,亲核试剂促进其活性物种的释放。