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一种新型拓扑异构酶I抑制剂DIA-001诱导癌细胞中DNA损伤介导的细胞周期阻滞和凋亡。

A novel topoisomerase I inhibitor DIA-001 induces DNA damage mediated cell cycle arrest and apoptosis in cancer cell.

作者信息

Liu Jiaqi, Geng Guohe, Liang Guang, Wang Ling, Luo Kuntian, Yuan Jian, Zhao Shiguang

机构信息

Department of Neurosurgery, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, China.

School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, China.

出版信息

Ann Transl Med. 2020 Feb;8(4):89. doi: 10.21037/atm.2019.12.138.

Abstract

BACKGROUND

DNA topoisomerase enzyme plays an essential role in controlling the DNA topology structure by binding to DNA and cutting the phosphate backbone of either one or both of the DNA strands. Here, we have identified a small molecule inhibitor, DIA-001, that directly binds to Topoisomerase 1 (Topo I) and promotes the Topo I-DNA adducts.

METHODS

In this study, we investigated the antitumor effects of DIA-001 using MTS assay and colony formation. We examined cell cycle of tumor cells with DIA-001 treatment by flow cytometry. And we investigated DNA damage and cell cycle marker protein after treatment with DIA-001 at different concentration and time point by western blot. Immunofluorescence was performance to detect the nuclear foci. The effects of DIA-001 on Topo I and Topo II activities were examined by DNA relaxation assays.

RESULTS

We demonstrate that DIA-001 inhibit DNA replication and arrest cell cycle progression at the G2/M phase by directly binds to Topo I and promotes the Topo I-DNA adducts. In addition, DIA-001 can activate the DNA damage response signaling cascade, resulting in apoptosis in treated cells.

CONCLUSIONS

Our findings show a novel compound for treatment of cancer cells with the potential as a chemotherapy candidate that is less toxic to normal cells.

摘要

背景

DNA拓扑异构酶通过与DNA结合并切割一条或两条DNA链的磷酸主链,在控制DNA拓扑结构中发挥着至关重要的作用。在此,我们鉴定出一种小分子抑制剂DIA-001,它能直接与拓扑异构酶1(Topo I)结合并促进Topo I-DNA加合物的形成。

方法

在本研究中,我们使用MTS法和集落形成实验来研究DIA-001的抗肿瘤作用。我们通过流式细胞术检测经DIA-001处理的肿瘤细胞的细胞周期。并且我们通过蛋白质免疫印迹法,在不同浓度和时间点用DIA-001处理后,研究DNA损伤和细胞周期标记蛋白。通过免疫荧光检测核灶。通过DNA松弛实验检测DIA-001对Topo I和Topo II活性的影响。

结果

我们证明DIA-001通过直接与Topo I结合并促进Topo I-DNA加合物的形成,抑制DNA复制并使细胞周期进程停滞在G2/M期。此外,DIA-001可激活DNA损伤反应信号级联反应,导致处理后的细胞凋亡。

结论

我们的研究结果显示了一种新型化合物,可用于治疗癌细胞,具有作为化疗候选药物的潜力,且对正常细胞毒性较小。

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