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暹罗牛油果种子提取物中的山竹子素E/BB对K562白血病细胞系中威尔姆斯瘤1蛋白表达的抑制作用。

Inhibitory effect of mammea E/BB from Mammea siamensis seed extract on Wilms' tumour 1 protein expression in a K562 leukaemic cell line.

作者信息

Rungrojsakul Methee, Saiai Aroonchai, Ampasavate Chadarat, Anuchapreeda Songyot, Okonogi Siriporn

机构信息

a Department of Pharmaceutical Science , Faculty of Pharmacy, Chiang Mai University , Chiang Mai 50200 , Thailand.

b Department of Chemistry , Faculty of Science, Chiang Mai University , Chiang Mai 50200 , Thailand.

出版信息

Nat Prod Res. 2016;30(4):443-7. doi: 10.1080/14786419.2015.1017491. Epub 2015 Mar 4.

Abstract

Mammea siamensis is used in traditional Thai medicine. This study was designed to extract and isolate an active compound from the M. siamensis seeds and to investigate its activity on Wilms' tumour 1 (WT1) protein expression in K562 cells. WT1 is a transcription factor that stimulates cell proliferation. The ethanol saraphi seed (ESS) extract was fractionated using n-hexane, ethyl acetate, n-butanol and water to obtain n-hexane saraphi seed (HSS), ethyl acetate saraphi seed (EASS), n-butanol saraphi seed (BSS), and water saraphi seed (WSS) extracts, respectively. The ESS, HSS and EASS extracts had strong cytotoxic effects on K562 cells in the MTT assay. All three fractions decreased WT1 protein levels and decreased total cell numbers. The HSS extract decreased the WT1 protein levels in a time- and dose-dependent manner. HPLC and NMR analyses indicated that the active compound of HSS was mammea E/BB. M. siamensis seeds are thus identified as a promising source of bioactive compounds for potential inhibition of WT1 protein expression.

摘要

暹罗山竹子在泰国传统医学中有所应用。本研究旨在从暹罗山竹子种子中提取并分离出一种活性化合物,并研究其对K562细胞中威尔姆斯瘤1(WT1)蛋白表达的影响。WT1是一种刺激细胞增殖的转录因子。使用正己烷、乙酸乙酯、正丁醇和水对乙醇提取的山竹子种子(ESS)提取物进行分级分离,分别获得正己烷提取的山竹子种子(HSS)、乙酸乙酯提取的山竹子种子(EASS)、正丁醇提取的山竹子种子(BSS)和水提取的山竹子种子(WSS)提取物。在MTT试验中,ESS、HSS和EASS提取物对K562细胞具有较强的细胞毒性作用。这三个组分均降低了WT1蛋白水平并减少了细胞总数。HSS提取物以时间和剂量依赖的方式降低了WT1蛋白水平。高效液相色谱(HPLC)和核磁共振(NMR)分析表明,HSS的活性化合物是山竹子素E/BB。因此,暹罗山竹子种子被确定为一种有前景的生物活性化合物来源,可能对WT1蛋白表达具有抑制作用。

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