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黄酮类化合物对 DNA 拓扑异构酶的作用:癌症治疗的最新进展和未来展望。

Flavonoids acting on DNA topoisomerases: recent advances and future perspectives in cancer therapy.

机构信息

Laboratory of Systems Approaches and Non Communicable Diseases, IRCCS San Raffaele Pisana, Via di Valcannuta, 247, I-00166 Roma, Italia.

出版信息

Curr Med Chem. 2012;19(31):5287-93. doi: 10.2174/092986712803833272.

Abstract

Flavonoids, secondary metabolites ubiquitously produced in the plant kingdom, are low molecular weight polyphenolic molecules. They are characterized by variable chemical structures and show a vast array of biological activities (i.e... antiviral, antiinflammatory, antitumor, antimicrobial, estrogenic, antiestrogenic, antioxidant, mutagenic and antimutagenic) targeting different pathways. Some of these compounds such as Genistein, Daidzein or its synthetic derivative Phenoxodiol as well as Luteolin and Quercetin are able to inhibit DNA topoisomerases. This review discusses that Flavonoids targeting DNA topoisomerases may lead to novel drug development with anticancer potential.

摘要

类黄酮是植物界中普遍存在的次生代谢物,是一类低分子量的多酚类分子。它们的化学结构多变,表现出广泛的生物活性(如抗病毒、抗炎、抗肿瘤、抗菌、雌激素、抗雌激素、抗氧化、致突变和抗突变),针对不同的途径。其中一些化合物,如染料木黄酮、大豆苷元和其合成衍生物 Phenoxodiol 以及木犀草素和槲皮素,能够抑制 DNA 拓扑异构酶。这篇综述讨论了靶向 DNA 拓扑异构酶的类黄酮可能会导致具有抗癌潜力的新型药物开发。

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