Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Avenida Professor Egas Moniz, 1649-028 Lisboa, Portugal.
iBB-Institute for Bioengineering and Biosciences, Departmento de Bioengenharia, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa, Portugal.
Metallomics. 2020 Jun 24;12(6):974-987. doi: 10.1039/d0mt00064g.
The anticancer, antimicrobial and antiplasmodial activities of six gold(iii) bis(dithiolene) complexes were studied. Complexes 1-6 showed relevant anticancer properties against A2780/A2780cisR ovarian cancer cells (IC50 values of 0.08-2 μM), also being able to overcome cisplatin resistance in A2780cisR cells. Complex 1 also exhibited significant antimicrobial activity against Staphylococcus aureus (minimum inhibitory concentration (MIC) values of 12.1 ± 3.9 μg mL-1) and both Candida glabrata and Candida albicans (MICs of 9.7 ± 2.7 and 19.9 ± 2.4 μg mL-1, respectively). In addition, all complexes displayed antiplasmodial activity against the Plasmodium berghei parasite liver stages, even exhibiting better results than the ones obtained using primaquine, an anti-malarial drug. Mechanistic studies support the idea that thioredoxin reductase, but not DNA, is a possible target of these complexes. Complex 1 is stable under biological conditions, which would be important if this compound is ever to be considered as a drug. Overall, the results obtained evidenced the promising biological activity of complex 1, which might have potential as a novel anticancer, antimicrobial and antiplasmodial agent to be used as an alternative to current therapeutics.
六种金(III)双二硫烯配合物的抗癌、抗菌和抗疟原虫活性研究。配合物 1-6 对 A2780/A2780cisR 卵巢癌细胞具有相关的抗癌特性(IC50 值为 0.08-2 μM),并且能够克服 A2780cisR 细胞中的顺铂耐药性。配合物 1 还对金黄色葡萄球菌(最小抑菌浓度(MIC)值为 12.1 ± 3.9 μg mL-1)和光滑假丝酵母和白色假丝酵母(MIC 值分别为 9.7 ± 2.7 和 19.9 ± 2.4 μg mL-1)表现出显著的抗菌活性。此外,所有配合物对疟原虫伯氏疟原虫肝期均表现出抗疟原虫活性,甚至比使用抗疟药物伯氨喹的效果更好。机制研究支持这样一种观点,即硫氧还蛋白还原酶而不是 DNA 是这些配合物的可能靶标。配合物 1 在生物条件下稳定,如果该化合物被认为是一种药物,这将是很重要的。总的来说,研究结果证明了配合物 1 具有有前途的生物学活性,它可能具有作为一种新型抗癌、抗菌和抗疟原虫药物的潜力,可作为当前治疗方法的替代。