Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences, Laboratory for Inorganic Chemical Biology, 75005, Paris, France.
Institut Curie, PSL University, CNRS UMR 144, 75248, Paris, France.
Chemistry. 2020 Apr 16;26(22):4997-5009. doi: 10.1002/chem.201904877. Epub 2020 Mar 26.
Cancer is one of the main causes of death worldwide. Chemotherapy, despite its severe side effects, is to date one of the leading strategies against cancer. Metal-based drugs present several potential advantages when compared to organic compounds and they have gained trust from the scientific community after the approval on the market of the drug cisplatin. Recently, we reported the ruthenium complex (Ru(DIP) (sq) (where DIP is 4,7-diphenyl-1,10-phenantroline and sq is semiquinonate) with a remarkable potential as chemotherapeutic agent against cancer, both in vitro and in vivo. In this work, we analyse a structurally similar compound, namely Ru(DIP) (mal), carrying the flavour-enhancing agent approved by the FDA, maltol (mal). To possess an FDA approved ligand is crucial for a complex, whose mechanism of action might include ligand exchange. Herein, we describe the synthesis and characterisation of Ru(DIP) (mal), its stability in solutions and under conditions that resemble the physiological ones, and its in-depth biological investigation. Cytotoxicity tests on different cell lines in 2D model and on HeLa MultiCellular Tumour Spheroids (MCTS) demonstrated that our compound has higher activity than cisplatin, inspiring further tests. Ru(DIP) (mal) was efficiently internalised by HeLa cells through a passive transport mechanism and severely affected the mitochondrial metabolism.
癌症是全球主要死亡原因之一。化疗是目前对抗癌症的主要策略之一,尽管它有严重的副作用。与有机化合物相比,金属基药物具有若干潜在优势,并且在顺铂(cisplatin)上市获得科学界信任后,金属基药物得到了发展。最近,我们报道了钌配合物([Ru(DIP)(sq)](PF ),其中 DIP 是 4,7-二苯基-1,10-菲咯啉,sq 是半醌)具有作为抗癌药物的显著潜力,无论是在体外还是在体内。在这项工作中,我们分析了一种结构相似的化合物,即[Ru(DIP)(mal)](PF ),它含有 FDA 批准的风味增强剂麦芽酚(mal)。对于一种可能包括配体交换的作用机制的配合物来说,具有 FDA 批准的配体是至关重要的。本文描述了[Ru(DIP)(mal)](PF )的合成和表征,它在溶液中的稳定性以及在类似于生理条件下的稳定性,并对其进行了深入的生物学研究。在 2D 模型和 HeLa 多细胞肿瘤球体(MCTS)上的不同细胞系的细胞毒性测试表明,我们的化合物比顺铂具有更高的活性,激发了进一步的测试。[Ru(DIP)(mal)](PF )通过被动运输机制被 HeLa 细胞有效内化,并严重影响了线粒体代谢。