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臭椿树皮中2-二氢苦木素对U251的抗肿瘤活性

Antitumour activity of 2-dihydroailanthone from the bark of Ailanthus altissima against U251.

作者信息

Wang Ruxing, Xu Qian, Liu Lei, Liang Xiujun, Cheng Luyang, Zhang Manli, Shi Qingwen

机构信息

a Department of Medicinal Natural Product Chemistry , School of Pharmaceutical Sciences, Hebei Medical University , Shijiazhuang Hebei Province , China ;

b Hebei Province Key Laboratory of Research and Development for Chinese Medicine , Institute of Chinese Materia Medica, Chengde Medical College , Chengde , Hebei Province China ;

出版信息

Pharm Biol. 2016 Sep;54(9):1641-8. doi: 10.3109/13880209.2015.1110827. Epub 2016 Mar 9.

Abstract

Context The bark of Ailanthus altissima (Mill.) Swingle (Simaroubaceae) is traditionally used to treat ascariasis, diarrhoea, spermatorrhoea, bleeding and gastrointestinal diseases. Objective The objective of this study is to investigate the antitumour activity and mechanism of 2-dihydroailanthone isolated from A. altissima. Materials and methods The U251 cells were treated with 1.00, 4.00 and 8.00 μg/mL of 2-dihydroailanthone for 48 h and the normal cells treated with 20.00 μg/mL of 2-dihydroailanthone were tested as well. Proliferation inhibition of 2-dihydroailanthone on the cells was tested by MTT. Apoptosis and cell-cycle distribution in U251 cells with 1.00, 3.00 and 5.80 μg/mL of 2-dihydroailanthone for 48 h were determined by flow cytometry, respectively. The expression of the apoptosis-related genes and proteins was analysed by RT-PCR and Western blot method, respectively. Results MTT assay revealed that 2-dihydroailanthone inhibited U251 cells proliferation. The cell viability of U251 cells was 62.82, 31.34 and 25.58%, and that of three normal cells was 72.75, 82.74 and 44.92%, respectively. Flow cytometry assay showed that 2-dihydroailanthone induced apoptosis and G0/G1 phase cycle arrest towards U251 cells. The late apoptotic cells were 11.37, 21.73 and 33.83%, and the cells cycle distributed in the G0/G1 accounted for 48.85, 62.77 and 64.40%, respectively. The Western blot and RT-PCR assay showed that up-regulation of pro-apoptotic bax protein and down-regulation of anti-apoptotic bcl-2 protein as well as their mRNA on U251 cells might be related to the apoptosis induction and proliferation inhibition. Conclusion An important bioactive component, 2-dihydroailanthone, has antitumour effects, enlightening a novel source of phytomedicines in tumour therapy.

摘要

背景 臭椿(苦木科)的树皮传统上用于治疗蛔虫病、腹泻、遗精、出血和胃肠道疾病。目的 本研究旨在探讨从臭椿中分离得到的2-二氢臭椿酮的抗肿瘤活性及其作用机制。材料与方法 用1.00、4.00和8.00μg/mL的2-二氢臭椿酮处理U251细胞48小时,并以20.00μg/mL的2-二氢臭椿酮处理正常细胞作为对照。采用MTT法检测2-二氢臭椿酮对细胞增殖的抑制作用。分别用流式细胞术检测1.00、3.00和5.80μg/mL的2-二氢臭椿酮处理U251细胞48小时后的凋亡及细胞周期分布情况。分别采用RT-PCR和Western blot法分析凋亡相关基因和蛋白的表达。结果 MTT法显示2-二氢臭椿酮抑制U251细胞增殖。U251细胞的存活率分别为62.82%、31.34%和25.58%,三种正常细胞的存活率分别为72.75%、82.74%和(44.92%)。流式细胞术检测显示2-二氢臭椿酮诱导U251细胞凋亡并使其停滞于G0/G1期。晚期凋亡细胞分别为1(1.37%)、2(1.73%)和3(3.83%),细胞周期分布于G0/G1期的分别占4(8.85%)、6(2.77%)和6(4.40%)。Western blot和RT-PCR检测显示,U251细胞上促凋亡蛋白bax上调、抗凋亡蛋白bcl-2及其mRNA下调,这可能与诱导凋亡和抑制增殖有关。结论 2-二氢臭椿酮是一种重要的生物活性成分,具有抗肿瘤作用,为肿瘤治疗中的植物药提供了新的来源。

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