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Chrysosplenetin 的体外和计算机评估与 DNA 相互作用、拓扑异构酶 I 和 II 抑制特性。

In vitro and in silico assessment of DNA interaction, topoisomerase I and II inhibition properties of chrysosplenetin.

机构信息

Hacettepe University, Faculty of Pharmacy, Department of Pharmacognosy, Sıhhiye, Ankara, TR-06100 Ankara, Turkey.

Karadeniz Technical University, Faculty of Pharmacy, Department of Biochemistry, Trabzon, Turkey.

出版信息

Int J Biol Macromol. 2020 Nov 15;163:1053-1059. doi: 10.1016/j.ijbiomac.2020.07.049. Epub 2020 Jul 13.

Abstract

Chrysosplenetin is a methoxyflavone with reported anti-cancer effect. We tested its cytotoxic effect on the MCF-7 breast cancer cell line, and determined its effect on DNA intercalation and on the activity of topoisomerases I and II. The compound inhibited proliferation MCF-7 with an IC value of 0.29 μM. Chrysosplenetin did not initiate plasmid DNA cleavage but, in a concentration-dependent manner, protected plasmid DNA against damage induced by Fenton reagents. Furthermore, it possessed dual Topoisomerase I and II inhibitory properties. Especially, it inhibited topoisomerase II by 83-96% between the range 12.5-100 μM. In the light of these experimental findings, molecular docking studies were performed to understand binding mode, interactions and affinity of chrysosplenetin with DNA, and with topoisomerases I and II. These studies showed that of 4-chromone core and the hydroxyl and methoxy groups important for both intercalation with DNA and topoisomerase I and II inhibition.

摘要

金合欢素是一种甲氧基黄酮,具有报道的抗癌作用。我们测试了它对 MCF-7 乳腺癌细胞系的细胞毒性作用,并确定了它对 DNA 嵌入和拓扑异构酶 I 和 II 活性的影响。该化合物对 MCF-7 的增殖具有抑制作用,IC 值为 0.29 μM。金合欢素不会引发质粒 DNA 切割,但会以浓度依赖的方式保护质粒 DNA 免受 Fenton 试剂诱导的损伤。此外,它具有双重拓扑异构酶 I 和 II 抑制特性。特别是,它在 12.5-100 μM 范围内抑制拓扑异构酶 II 的作用达 83-96%。根据这些实验结果,进行了分子对接研究,以了解金合欢素与 DNA 以及与拓扑异构酶 I 和 II 的结合模式、相互作用和亲和力。这些研究表明,4-色酮核心以及对与 DNA 嵌入和拓扑异构酶 I 和 II 抑制都很重要的羟基和甲氧基基团。

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