Lu Q-B, Kalantari S, Wang C-R
Department of Physics, University of Waterloo, 200 University Avenue West, Waterloo, Ontario, N2L 3G1, Canada.
Mol Pharm. 2007 Jul-Aug;4(4):624-8. doi: 10.1021/mp070040a. Epub 2007 Jun 9.
The cytotoxicity of cisplatin as a very effective chemotherapeutic anticancer drug is known to arise from its capacity to damage DNA. However, the mechanism of action of cisplatin at the molecular level, in particular, the reaction dynamics of cisplatin with DNA, remains elusive, and the reason why cisplatin binds to the guanine bases rather than to S-donor ligands available in cells remains a mystery. Using time-resolved femtosecond laser spectroscopy, for the first time, we reveal the high reactivity of cisplatin with electrons and its preferential electron-transfer reaction with the DNA guanine base. The results not only provide a molecular mechanistic understanding of cisplatin in cancer therapy but may have far-reaching significance for understanding the role of polar molecules such as NH3 and NH2 in biological reactions.
顺铂作为一种非常有效的化疗抗癌药物,其细胞毒性已知源于其损伤DNA的能力。然而,顺铂在分子水平上的作用机制,特别是顺铂与DNA的反应动力学,仍然难以捉摸,并且顺铂与鸟嘌呤碱基结合而不是与细胞中可用的硫供体配体结合的原因仍然是个谜。我们首次使用时间分辨飞秒激光光谱法揭示了顺铂与电子的高反应性及其与DNA鸟嘌呤碱基的优先电子转移反应。这些结果不仅提供了对顺铂在癌症治疗中的分子机制的理解,而且对于理解诸如NH3和NH2等极性分子在生物反应中的作用可能具有深远的意义。