Department of Chemistry, Imperial College London, White City Campus, London, W12 0BZ, United Kingdom.
Department of Mathematics, Imperial College London, South Kensington Campus, London, SW7 2AZ, United Kingdom.
Chemistry. 2024 Nov 7;30(62):e202402465. doi: 10.1002/chem.202402465. Epub 2024 Oct 16.
Current anticancer therapies suffer from issues such as off-target side effects and the emergence of drug resistance; therefore, the discovery of alternative therapeutic approaches is vital. These can include the development of drugs with different modes of action, and the exploration of new biomolecular targets. For the former, there has been increasing interest in drugs that are activated by an external stimulus (e. g. light irradiation) to generate cytotoxic chemicals such as reactive oxygen species (ROS). For the latter, significant efforts are being directed to explore non-canonical DNA and RNA structures (e. g. guanine-quadruplexes), as alternative biomolecular targets. Herein we report the synthesis of a library of 21 new platinum(II)-Salphen complexes (square planar platinum(II) complexes coordinated to tetradentate O,N,N,O-Schiff base ligands), and the investigation, for all complexes, of their photophysical and photochemical properties, their interactions with duplex and quadruplex DNA, and their cytotoxicity against HeLa cancer cells both in the dark and upon light irradiation. Thanks to the intrinsic phosphorescence of the platinum(II) complexes, confocal microscopy was used for six of the complexes to determine their cellular permeability and localisation in two cancer cell lines (HeLa and U2OS). Altogether, these studies have allowed us to identify two lead platinum(II) complexes with high guanine-quadruplex DNA affinity and selectivity, good cell permeability and nuclear localisation, and high cytotoxicity against HeLa cancer cells upon irradiation with no detected cytotoxicity in the dark.
当前的抗癌疗法存在一些问题,例如靶向副作用和耐药性的出现;因此,发现替代治疗方法至关重要。这些方法可以包括开发具有不同作用模式的药物,以及探索新的生物分子靶标。对于前者,人们越来越关注那些可以被外部刺激(例如光辐射)激活以产生细胞毒性化学物质如活性氧(ROS)的药物。对于后者,人们正在努力探索非典型的 DNA 和 RNA 结构(例如鸟嘌呤四联体)作为替代生物分子靶标。在此,我们报告了 21 种新的铂(II)-Salphen 配合物(配位到四齿 O,N,N,O-Schiff 碱配体的平面正方形铂(II)配合物)的合成,并对所有配合物的光物理和光化学性质、与双链和四链 DNA 的相互作用以及在黑暗和光照下对 HeLa 癌细胞的细胞毒性进行了研究。由于铂(II)配合物的固有磷光性质,我们使用共聚焦显微镜对其中的六种配合物进行了研究,以确定它们在两种癌细胞系(HeLa 和 U2OS)中的细胞通透性和定位。总的来说,这些研究使我们能够确定两种具有高鸟嘌呤四联体 DNA 亲和力和选择性、良好的细胞通透性和核定位以及对 HeLa 癌细胞高细胞毒性的先导铂(II)配合物,在黑暗中没有检测到细胞毒性,在光照下才有。