Clinical Research Centre, Medical University of Bialystok, 15-276 Bialystok, Poland.
Prof. Wacław Dąbrowski Institute of Agricultural and Food Biotechnology-State Research Institute, 02-532 Warsaw, Poland.
Int J Mol Sci. 2022 Dec 26;24(1):391. doi: 10.3390/ijms24010391.
Anthracyclines currently play a key role in the treatment of many cancers, but the limiting factor of their use is the widespread phenomenon of drug resistance and untargeted toxicity. Flavonoids have pleiotropic, beneficial effects on human health that, apart from antioxidant activity, are currently considered small molecules-starting structures for drug development and enhancers of conventional therapeutics. This paper is a review of the current and most important data on the participation of a selected series of flavonoids: chrysin, apigenin, kaempferol, quercetin and myricetin, which differ in the presence of an additional hydroxyl group, in the formation of a synergistic effect with anthracycline antibiotics. The review includes a characterization of the mechanism of action of flavonoids, as well as insight into the physicochemical parameters determining their bioavailability in vitro. The crosstalk between flavonoids and the molecular activity of anthracyclines discussed in the article covers the most important common areas of action, such as (1) disruption of DNA integrity (genotoxic effect), (2) modulation of antioxidant response pathways, and (3) inhibition of the activity of membrane proteins responsible for the active transport of drugs and xenobiotics. The increase in knowledge about the relationship between the molecular structure of flavonoids and their biological effect makes it possible to more effectively search for derivatives with a synergistic effect with anthracyclines and to develop better therapeutic strategies in the treatment of cancer.
蒽环类药物目前在许多癌症的治疗中发挥着关键作用,但它们的使用受到限制,原因是存在广泛的耐药性和非靶向毒性现象。类黄酮对人类健康具有多种有益作用,除了抗氧化活性外,目前还被认为是药物开发的小分子起始结构和常规治疗的增强剂。本文综述了一系列选定类黄酮(白杨素、芹菜素、山奈酚、槲皮素和杨梅素)参与形成协同作用的最新和最重要数据,这些类黄酮在结构上的差异在于是否存在额外的羟基,从而与蒽环类抗生素形成协同作用。本文综述了类黄酮的作用机制特征,并深入了解了决定其体外生物利用度的物理化学参数。本文讨论了类黄酮与蒽环类抗生素分子活性之间的串扰,涵盖了最重要的共同作用领域,如(1)破坏 DNA 完整性(遗传毒性作用)、(2)调节抗氧化反应途径,以及(3)抑制负责药物和外源性物质主动转运的膜蛋白的活性。关于类黄酮的分子结构与其生物学效应之间关系的知识增加,使得更有效地寻找与蒽环类药物具有协同作用的衍生物并制定更好的癌症治疗策略成为可能。