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Epigallocatechin‐3‐gallate induces telomere shortening and clastogenic damage in glioblastoma cells

机译:Epigallocatechin-3-gallate诱导端粒缩短和抗植物损伤在胶质母细胞瘤细胞中

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摘要

Epigallocatechingallate (EGCG) is the major polyphenol in green tea, to which many anticancer features, such as antioxidative, antigenotoxic, and antiangiogenetic properties, are attributed. Moreover, it is also well known as a telomerase inhibitor. In this work, we have chronically treated U251 glioblastoma cells with low, physiologically realistic concentrations, of EGCG, in order to investigate its effects both on telomeres and on genome integrity. Inhibition of telomerase activity caused telomere shortening, ultimately leading to senescence and telomere dysfunction at 98?days. Remarkably, we have observed DNA damage through an increase of phosphorylation of γ‐H2AX histone and micronuclei also with doses and at timepoints when telomere shortening was not present. Therefore, we concluded that this DNA damage was not correlated with telomere shortening and that EGCG treatment induced not only an increase of telomere‐shortening‐induced senescence but also telomere‐independent genotoxicity. This study questions the common knowledge about EGCG properties, but confirms the few works that indicated the clastogenic properties of this molecule, probably due to DNA reductive damage and topoisomerase II poisoning. Environ. Mol. Mutagen., 60:683–692, 2019. ? 2019 Wiley Periodicals, Inc.
机译:Epigallocatechingallate(EGCG)是绿茶中的主要多酚,许多抗氧化,抗抗毒性和抗血管生成特性,归因于抗氧化,抗毒性和抗血管生成特征。此外,它也是众所周知的端粒酶抑制剂。在这项工作中,我们在慢性治疗U251胶质母细胞瘤细胞,EGCG的低,生理学上现实浓度,以研究其对端粒和基因组完整性的影响。抑制端粒酶活性导致端粒缩短,最终导致98℃的衰老和端粒功能障碍。值得注意的是,当不存在端粒缩短时,我们通过增加γ-H2AX组蛋白和微核的磷酸化而观察到DNA损伤。因此,我们得出结论,这种DNA损伤与端粒缩短不相关,并且EGCG治疗不仅促进了端粒缩短诱导的衰老而且均有独立的遗传毒性。本研究提出了关于EGCG性质的常识,但确认了指示该分子的抗植物特性的少数作品,可能是由于DNA还原损伤和拓扑异构酶II中毒。环境。摩尔。 mutagen,60:683-692,2019。? 2019 Wiley期刊,Inc。

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