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(-)-Xanthatin 通过抑制拓扑异构酶 IIα 和产生活性氧诱导 MDA-MB-231 乳腺癌细胞中 GADD45γ 肿瘤抑制基因的上调。

(-)-Xanthatin up-regulation of the GADD45γ tumor suppressor gene in MDA-MB-231 breast cancer cells: role of topoisomerase IIα inhibition and reactive oxygen species.

机构信息

Department of Molecular Biology, Daiichi University of Pharmacy, 22-1 Tamagawa-cho, Minami-ku, Fukuoka 815-8511, Japan.

出版信息

Toxicology. 2013 Mar 8;305:1-9. doi: 10.1016/j.tox.2012.12.019. Epub 2013 Jan 8.

DOI:10.1016/j.tox.2012.12.019
PMID:23313378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4030303/
Abstract

Previously, we reported that (-)-xanthatin, a naturally occurring xanthanolide present in the Cocklebur plant, exhibits potent anti-proliferative effects on human breast cancer cells, accompanied by an induction of the growth arrest and DNA damage-inducible gene 45γ (GADD45γ), recognized recently as a novel tumor suppressor gene. However, the mechanisms mediating this activation were unknown. Topoisomerase IIα (Topo IIα) inhibition has been reported to produce a cell death response accompanied by an atypical DNA laddering fragmentation profile, similar to that noted previously for (-)-xanthatin. Therefore we hypothesized that (-)-xanthatin's GADD45γ activation was mediated through the Topo IIα pathway. Here, we identify that (-)-xanthatin does function as a catalytic inhibitor of Topo IIα, promoting DNA damage. In addition, reactive oxygen species (ROS) were elevated in cells treated with this agent. Mechanistically, it was determined that the induced levels of GADD45γ mRNA resulting from (-)-xanthatin exposures were stabilized by coordinately produced ROS, and that the consequent induction of GADD45γ mRNA, GADD45γ protein and ROS generation were abrogated by co-treatment with N-acetyl-l-cysteine. Taken together, the data support the concept that Topo IIα inhibition by (-)-xanthatin is a trigger that stimulates expression of DNA damage-inducible GADD45γ mRNA and that concomitantly produced ROS act downstream to further enhance the GADD45γ mRNA/GADD45γ protein induction process, resulting in breast cancer cell death.

摘要

先前,我们报道了(-)-黄烷酮,一种存在于苍耳植物中的天然黄烷酮醇,对人乳腺癌细胞具有很强的抗增殖作用,同时诱导生长停滞和 DNA 损伤诱导基因 45γ(GADD45γ),最近被认为是一种新型肿瘤抑制基因。然而,介导这种激活的机制尚不清楚。拓扑异构酶 IIα(Topo IIα)抑制已被报道会产生细胞死亡反应,同时伴有非典型的 DNA 梯状片段化谱,与先前报道的(-)-黄烷酮相似。因此,我们假设(-)-黄烷酮的 GADD45γ 激活是通过 Topo IIα 途径介导的。在这里,我们确定(-)-黄烷酮确实可以作为 Topo IIα 的催化抑制剂,促进 DNA 损伤。此外,该药物处理的细胞中活性氧(ROS)水平升高。从机制上讲,确定(-)-黄烷酮暴露导致的 GADD45γ mRNA 水平升高是由协同产生的 ROS 稳定的,并且随后诱导的 GADD45γ mRNA、GADD45γ 蛋白和 ROS 生成被 N-乙酰-L-半胱氨酸共同处理所阻断。总之,这些数据支持这样一种概念,即(-)-黄烷酮对 Topo IIα 的抑制是一种触发因素,可刺激 DNA 损伤诱导的 GADD45γ mRNA 的表达,同时产生的 ROS 则进一步增强 GADD45γ mRNA/GADD45γ 蛋白诱导过程,导致乳腺癌细胞死亡。

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