Shaabani Mahmoud, Mousavi Seyed Hadi, Azizi Majid, Ashraf Jafari Ali
Department of Horticulture Science and Agronomy, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Medical Toxicology Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad 917794-8564, Iran.
Avicenna J Phytomed. 2020 Nov-Dec;10(6):594-603.
Glioblastoma multiforme (GBM) is the most aggressive and malignant brain tumor and has a poor prognosis. This study was aimed to investigate the cytotoxic effects of Boiss. ) extracts in GBM U87 cell line.
The extracts of obtained by two different ways of Soxhlet and soaked. The cytotoxic effects of extracts were measured using MTT assay following treatment for different times of exposure (24, 48, and 72 hr) and at different concentrations of extracts. The effects of extracts on cellular oxidative stress were also evaluated by measuring cellular ROS levels. Furthermore, cellular death and apoptosis were studied by sub G1 analysis and Annexin V-FITC/propidium iodide (PI) staining using flow cytometry method, respectively. Characterization of the extracts was carried out using gas chromatography/mass spectrometry (GC/MS) analysis by Agilent GC-MSD system.
Our results indicated that extracts decreased U87 cell viability in a time- and dose-dependent manner. Moreover, treatment with extracted by Soxhlet for 24 and 48 hr significantly increased the levels of cellular ROS and Sub G1 population (p<0.001-0.05 for all cases). Furthermore, GC/MS analysis revealed that essential oils of mainly consisted of β-caryophellene, α-pinene and limonene.
Our findings demonstrated that extracts can exert cytotoxic effects against GBM U87 cell line in a time- and concentration-dependent manner, and these effects may be mediated through intracellular ROS accumulating. However, further studies should be performed to confirm the efficacy and exact mechanism of action of the extracts.
多形性胶质母细胞瘤(GBM)是最具侵袭性和恶性的脑肿瘤,预后较差。本研究旨在探讨[植物名称未完整给出]提取物对GBM U87细胞系的细胞毒性作用。
通过索氏提取法和浸泡法两种不同方式获得[植物名称未完整给出]提取物。在不同暴露时间(24、48和72小时)和不同提取物浓度处理后,使用MTT法测定提取物的细胞毒性作用。还通过测量细胞内活性氧(ROS)水平评估提取物对细胞氧化应激的影响。此外,分别采用流式细胞术通过亚G1期分析和膜联蛋白V-异硫氰酸荧光素/碘化丙啶(PI)染色研究细胞死亡和凋亡情况。使用安捷伦气相色谱-质谱联用(GC/MS)系统通过气相色谱/质谱(GC/MS)分析对提取物进行表征。
我们的结果表明,[植物名称未完整给出]提取物以时间和剂量依赖性方式降低U87细胞活力。此外,用索氏提取法提取的[植物名称未完整给出]处理24和48小时后,细胞内ROS水平和亚G1期细胞比例显著增加(所有情况p<0.001 - 0.05)。此外,GC/MS分析显示,[植物名称未完整给出]的挥发油主要由β-石竹烯、α-蒎烯和柠檬烯组成。
我们的研究结果表明,[植物名称未完整给出]提取物可对GBM U87细胞系产生时间和浓度依赖性的细胞毒性作用,这些作用可能通过细胞内ROS积累介导。然而,应进行进一步研究以证实提取物的疗效和确切作用机制。