School of Chemistry and Biosciences, University of Bradford, BD7 1DP, Bradford, UK.
Institute of Cancer Therapeutics, University of Bradford, BD7 1DP, Bradford, UK.
Chembiochem. 2022 Sep 16;23(18):e202200259. doi: 10.1002/cbic.202200259. Epub 2022 Aug 3.
The synthesis, characterisation, and evaluation of the in vitro cytotoxicity of five maleonitriledithiolate-based ruthenium metal complexes bearing various phosphine ligands towards two ovarian cancer cell lines (A2780 and A2780cisR), one non-small-cell lung cancer cell line (H460) and one normal prostate cell line (PNT2) are presented herein. These 18-electron complexes were designed with four water-soluble phosphine ligands to increase the water-solubility character of the corresponding electron-deficient ruthenium complex which showed great in vitro promises, and triphenylphosphine for comparison. The complexes with triphenylphosphine-3,3',3''-trisulfonic acid and triphenylphosphine present similar cytotoxicity compared to the 16-electron precursor, with equal cytotoxicity to both A2780 and A2780cisR. Hints at the mechanism of action suggest an apoptotic pathway based on reactive oxygen species (ROS) production. No toxicity was observed in preliminary in vivo pilot studies for these two complexes in subcutaneous A2780 and A2780cisR xenograft models, with some evidence of tumour growth delay.
本文介绍了五种基于马来二腈二硫醇的钌金属配合物的合成、表征和体外细胞毒性评价,这些配合物具有不同的膦配体,针对两种卵巢癌细胞系(A2780 和 A2780cisR)、一种非小细胞肺癌细胞系(H460)和一种正常前列腺细胞系(PNT2)进行了研究。这些 18 电子配合物设计了四个水溶性膦配体,以增加相应缺电子钌配合物的水溶性特征,这些配合物具有很大的体外应用前景,并与三苯基膦进行了比较。带有三苯基膦-3,3',3''-三磺酸和三苯基膦的配合物与 16 电子前体相比具有相似的细胞毒性,对 A2780 和 A2780cisR 的细胞毒性相等。作用机制的提示表明基于活性氧(ROS)产生的凋亡途径。在皮下 A2780 和 A2780cisR 异种移植模型中进行的这两种配合物的初步体内试验中未观察到毒性,有一些肿瘤生长延迟的证据。