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一种致命组合:一种具有DNA损伤活性的胸苷酸合成酶抑制剂。

A fatal combination: a thymidylate synthase inhibitor with DNA damaging activity.

作者信息

Ligasová Anna, Strunin Dmytro, Friedecký David, Adam Tomáš, Koberna Karel

机构信息

Institute of Molecular and Translational Medicine, Faculty of Medicine, Palacký University, Olomouc, 779 00, Czech Republic.

出版信息

PLoS One. 2015 Feb 11;10(2):e0117459. doi: 10.1371/journal.pone.0117459. eCollection 2015.

Abstract

2'-Deoxy-5-ethynyluridine (EdU) has been previously shown to be a cell poison whose toxicity depends on the particular cell line. The reason is not known. Our data indicates that different efficiency of EdU incorporation plays an important role. The EdU-mediated toxicity was elevated by the inhibition of 2'-deoxythymidine 5'-monophosphate synthesis. EdU incorporation resulted in abnormalities of the cell cycle including the slowdown of the S phase and a decrease in DNA synthesis. The slowdown but not the cessation of the first cell division after EdU administration was observed in all of the tested cell lines. In HeLa cells, a 10 μM EdU concentration led to the cell death in the 100% of cells probably due to the activation of an intra S phase checkpoint in the subsequent S phase. Our data also indicates that this EdU concentration induces interstrand DNA crosslinks in HeLa cells. We suppose that these crosslinks are the primary DNA damage resulting in cell death. According to our results, the EdU-mediated toxicity is further increased by the inhibition of thymidylate synthase by EdU itself at its higher concentrations.

摘要

2'-脱氧-5-乙炔基尿苷(EdU)先前已被证明是一种细胞毒素,其毒性取决于特定的细胞系。原因尚不清楚。我们的数据表明,EdU掺入效率的差异起着重要作用。2'-脱氧胸苷5'-单磷酸合成的抑制会提高EdU介导的毒性。EdU掺入导致细胞周期异常,包括S期减慢和DNA合成减少。在所有测试的细胞系中均观察到EdU给药后第一次细胞分裂减慢但未停止。在HeLa细胞中,10μM的EdU浓度导致100%的细胞死亡,这可能是由于随后S期内S期检查点的激活所致。我们的数据还表明,该EdU浓度会在HeLa细胞中诱导链间DNA交联。我们推测这些交联是导致细胞死亡的主要DNA损伤。根据我们的结果,在较高浓度下,EdU自身对胸苷酸合成酶的抑制会进一步增加EdU介导的毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/883b/4324964/3f1b5562bd1e/pone.0117459.g001.jpg

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