Zhang Zhuhong, Chen Si, Mei Hu, Xuan Jiekun, Guo Xiaoqing, Couch Letha, Dobrovolsky Vasily N, Guo Lei, Mei Nan
Division of Genetic and Molecular Toxicology, National Center for Toxicological Research, Jefferson, AR 72079, USA.
Division of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, AR 72079, USA.
Sci Rep. 2015 Sep 30;5:14633. doi: 10.1038/srep14633.
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.
美国国家毒理学计划进行的一项为期两年的生物测定表明,银杏叶提取物可增加小鼠肝脏肿瘤的发生率。在本研究中,我们评估了银杏叶提取物及其许多成分对人肝癌HepG2细胞的DNA损伤作用,并确定了其潜在机制。一项分子对接研究表明,银杏叶中的黄酮类成分槲皮素与拓扑异构酶II(Topo II)相互作用的潜力高于银杏叶的其他成分;通过生化分析研究Topo II酶抑制作用,证实了这一计算机模拟预测。此外,通过彗星试验和γ-H2A.X的诱导检测发现,槲皮素是HepG2细胞中最有效的DNA损伤诱导剂,其次是山奈酚和异鼠李素。在Topo II基因敲低的细胞中,银杏叶提取物或槲皮素引发的DNA损伤显著减少,表明DNA损伤与Topo II直接相关。用市售银杏叶提取物产品处理细胞时,也观察到了DNA损伤。我们的研究结果表明,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。