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Ginkgo biloba leaf extract induces DNA damage by inhibiting topoisomerase II activity in human hepatic cells

机译:银杏叶提取物通过抑制人肝细胞中的拓扑异构酶II活性诱导DNA损伤

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摘要

Ginkgo biloba leaf extract has been shown to increase the incidence in liver tumors in mice in a 2-year bioassay conducted by the National Toxicology Program. In this study, the DNA damaging effects of Ginkgo biloba leaf extract and many of its constituents were evaluated in human hepatic HepG2 cells and the underlying mechanism was determined. A molecular docking study revealed that quercetin, a flavonoid constituent of Ginkgo biloba, showed a higher potential to interact with topoisomerase II (Topo II) than did the other Ginkgo biloba constituents; this in silico prediction was confirmed by using a biochemical assay to study Topo II enzyme inhibition. Moreover, as measured by the Comet assay and the induction of γ-H2A.X, quercetin, followed by keampferol and isorhamnetin, appeared to be the most potent DNA damage inducer in HepG2 cells. In Topo II knockdown cells, DNA damage triggered by Ginkgo biloba leaf extract or quercetin was dramatically decreased, indicating that DNA damage is directly associated with Topo II. DNA damage was also observed when cells were treated with commercially available Ginkgo biloba extract product. Our findings suggest that Ginkgo biloba leaf extract- and quercetin-induced in vitro genotoxicity may be the result of Topo II inhibition.
机译:在国家毒理学计划进行的为期2年的生物测定中,银杏叶提取物已显示可增加小鼠肝肿瘤的发生率。在这项研究中,银杏叶提取物及其许多成分对人肝HepG2细胞的DNA破坏作用进行了评估,并确定了其潜在机制。一项分子对接研究表明,槲皮素是银杏叶的一种类黄酮成分,与拓扑异构酶II(Topo II)的相互作用潜力要高于其他银杏叶成分。通过使用生化分析研究Topo II酶抑制作用,证实了这种计算机模拟预测。此外,通过彗星试验和γ-H2A.X的诱导测量,槲皮素,其次是keampferol和异鼠李素,似乎是HepG2细胞中最有效的DNA损伤诱导剂。在Topo II组合式细胞中,由银杏叶提取物或槲皮素触发的DNA损伤显着降低,表明DNA损伤与Topo II直接相关。当用市售的银杏提取物处理细胞时,也观察到DNA损伤。我们的发现表明,银杏叶提取物和槲皮素诱导的体外遗传毒性可能是Topo II抑制的结果。

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