Dpt de Química Inorgànica i Orgànica, Secció de Química Inorgànica, Facultat de Química, Universitat de Barcelona, Martí i Franquès 1-11, 08028, Barcelona, Spain.
Dpt. of Biochemistry and Molecular Biomedicine, Faculty of Biology, Universitat de Barcelona, Av. Diagonal, 643, 08028, Barcelona, Spain.
Chemistry. 2020 Feb 11;26(9):1947-1952. doi: 10.1002/chem.201905325. Epub 2020 Jan 30.
Platinum-based chemotherapy persists to be the only effective therapeutic option against a wide variety of tumours. Nevertheless, the acquisition of platinum resistance is utterly common, ultimately cornering conventional platinum drugs to only palliative in many patients. Thus, encountering alternatives that are both effective and non-cross-resistant is urgent. In this work, we report the synthesis, reduction studies, and luminescent properties of a series of cyclometallated (C,N,N')Pt compounds derived from amine-imine ligands, and their remarkable efficacy at the high nanomolar range and complete lack of cross-resistance, as an intrinsic property of the platinacycle, against multiplatinum-resistant colorectal cancer (CRC) and castration-resistant prostate cancer (CRPC) metastatic cell lines generated for this work. We have also determined that the compounds are effective and selective for a broader cancer panel, including breast and lung cancer. Additionally, selected compounds have been further evaluated, finding a shift in their antiproliferative mechanism towards more cytotoxic and less cytostatic than cisplatin against cancer cells, being also able to oxidize cysteine residues and inhibit topoisomerase II, thereby holding great promise as future improved alternatives to conventional platinum drugs.
铂类化疗仍然是对抗多种肿瘤的唯一有效治疗选择。然而,获得铂耐药性是非常常见的,最终使传统的铂类药物在许多患者中仅具有姑息作用。因此,迫切需要寻找既有效又非交叉耐药的替代药物。在这项工作中,我们报告了一系列源自胺-亚胺配体的环金属化(C,N,N')Pt 化合物的合成、还原研究和发光性质,以及它们在高纳摩尔范围内的显著疗效和完全缺乏交叉耐药性,这是固有铂环的特性,对为这项工作生成的多铂耐药结直肠癌(CRC)和去势抵抗性前列腺癌(CRPC)转移性细胞系具有显著疗效。我们还确定,这些化合物对更广泛的癌症谱有效且具有选择性,包括乳腺癌和肺癌。此外,还进一步评估了选定的化合物,发现它们对癌细胞的增殖抑制作用与顺铂相比,更倾向于细胞毒性而非细胞静止性,并且能够氧化半胱氨酸残基并抑制拓扑异构酶 II,因此有望成为未来改善传统铂类药物的替代药物。