Organometallic Chemistry Laboratory for the Design of Catalysts and Therapeutics, INRS-Centre Armand-Frappier Santé Biotechnologie, Université du Québec, Laval, QC H7V 1B7, Canada.
Molecules. 2020 Jan 9;25(2):265. doi: 10.3390/molecules25020265.
Since the discovery of the anticancer potential of ruthenium-based complexes, several species were reported as promising candidates for the treatment of breast cancer, which accounts for the greatest number of new cases in women every year worldwide. Among these ruthenium complexes, species containing bioactive ligand(s) have attracted increasing attention due to their potential multitargeting properties, leading to anticancer drug candidates with a broader range of cellular targets/modes of action. This review of the literature aims at providing an overview of the rationally designed ruthenium-based complexes that have been reported to date for which ligands were carefully selected for the treatment of hormone receptor positive breast cancers (estrogen receptor (ER+) or progesterone receptor (PR+)). In addition, this brief survey highlights some of the most successful examples of ruthenium complexes reported for the treatment of triple negative breast cancer (TNBC), a highly aggressive type of cancer, regardless of if their ligands are known to have the ability to achieve a specific biological function.
自发现钌基配合物的抗癌潜力以来,已有多种物质被报道为治疗乳腺癌的有前途的候选物,乳腺癌是全球每年新发病例数最多的癌症。在这些钌配合物中,由于其潜在的多靶点特性,含有生物活性配体的物质引起了越来越多的关注,从而产生了具有更广泛细胞靶点/作用模式的抗癌药物候选物。本文对文献的综述旨在提供一个概述,即迄今为治疗激素受体阳性乳腺癌(雌激素受体 (ER+) 或孕激素受体 (PR+))而精心选择配体的合理设计的基于钌的配合物。此外,这个简要的调查突出了一些报道的治疗三阴性乳腺癌 (TNBC) 的最成功的钌配合物的例子,无论其配体是否具有实现特定生物学功能的能力,TNBC 是一种高度侵袭性的癌症。