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体外评估 OEO 和百里香酚在 2D 和 3D 细胞培养中的凋亡作用,并研究它们与 DNA 的相互作用模式。

In-vitro evaluation of apoptotic effect of OEO and thymol in 2D and 3D cell cultures and the study of their interaction mode with DNA.

机构信息

Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran.

Institute of Biotechnology, Shiraz University, Shiraz, Iran.

出版信息

Sci Rep. 2018 Oct 25;8(1):15787. doi: 10.1038/s41598-018-34055-w.

Abstract

Oliveria decumbens is an Iranian endemic plant used extensively in traditional medicine. Recently, some studies have been performed on biological effects of Oliveria essential oil (OEO). However, to our knowledge, the anticancer activity of OEO has not been reported. Based on our GC/MS analysis, the basic ingredients of OEO are thymol, carvacrol, p-cymene and γ-terpinene. Therefore, we used OEO and its main component, thymol, to explore their effects on cell growth inhibition and anticancer activity. Despite having a limited effect on L929 normal cells, OEO/thymol induced cytotoxicity in MDA-MB231 breast cancer monolayers (2D) and to a lesser extent in MDA-MB231 spheroids (3D). Flow cytometry, caspase-3 activity assay in treated monolayers/spheroids and also fluorescence staining and DNA fragmentation in treated monolayers demonstrated apoptotic death mode. Indeed, OEO/thymol increased the Reactive Oxygen Species (ROS) level leading to mitochondrial membrane potential (MMP, ΔΨm) loss, caspase-3 activation and DNA damage caused S-phase cell cycle arrest. Furthermore, immunoblotting studies revealed the activation of intrinsic and maybe extrinsic apoptosis pathways by OEO/thymol. Additionally, in-vitro experiments, indicated that OEO/thymol interacts with DNA via minor grooves confirmed by docking method. Altogether, our reports underlined the potential of OEO to be considered as a new candidate for cancer therapy.

摘要

倒地铃是一种伊朗特有植物,在传统医学中被广泛应用。最近,一些研究已经对奥利维亚精油(OEO)的生物效应进行了研究。然而,据我们所知,OEO 的抗癌活性尚未被报道。根据我们的 GC/MS 分析,OEO 的基本成分是百里香酚、香芹酚、对伞花烃和γ-萜品烯。因此,我们使用 OEO 和其主要成分百里香酚来探索它们对细胞生长抑制和抗癌活性的影响。尽管对 L929 正常细胞的作用有限,但 OEO/百里香酚在 MDA-MB231 乳腺癌单层(2D)中诱导细胞毒性,在 MDA-MB231 球体(3D)中诱导毒性的程度较小。流式细胞术、处理单层/球体中的 caspase-3 活性测定以及处理单层中的荧光染色和 DNA 片段化显示了细胞凋亡死亡模式。事实上,OEO/百里香酚增加了活性氧物种(ROS)水平,导致线粒体膜电位(MMP,ΔΨm)丧失、caspase-3 激活和 S 期细胞周期停滞引起的 DNA 损伤。此外,免疫印迹研究表明 OEO/百里香酚通过内在和可能的外在凋亡途径激活。此外,体外实验表明,OEO/百里香酚通过对接方法证实通过小沟与 DNA 相互作用。总之,我们的报告强调了 OEO 作为癌症治疗新候选药物的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c320/6202332/a2bced2e5fc5/41598_2018_34055_Fig1_HTML.jpg

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