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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Safranal, a Crocus sativus L constituent suppresses the growth of K-562 cells of chronic myelogenous leukemia. In silico and in vitro study
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Safranal, a Crocus sativus L constituent suppresses the growth of K-562 cells of chronic myelogenous leukemia. In silico and in vitro study

机译:Safranal,一种番红花L成分,可抑制慢性粒细胞性白血病K-562细胞的生长。计算机和体外研究

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Crocin, a main constituent of Crocus sativus L (saffron), has been found to inhibit the growth of K-562 human chronic myelogenous leukemia (CML) cells expressing Bcr-Abl protein tyrosine kinase activity. The aim of our study is to investigate the ability of the bioactive saffron's constituents, crocin (CRC) and safranal (SFR), to inhibit the Bcr-Abl protein activity employing an in silico approach, as well as the in vitro effect of these compounds on K-562 growth and gene expression of Bcr-Abl. In silica molecular docking studies revealed that mostly SFR can be attached to Bcr-Abl protein, positioned inside the protein's binding cavity at the same place with the drug used in the treatment of CML, imatinib mesylate (IM). The predicted polar interactions and hydrophobic contacts constructing a hydrophobic cavity inside the active site, explain the observed inhibitory activity. Cytotoxicity experiments showed that SFR and CRC mediate cytotoxic response to K562 cells. In vitro studies on the expression of Bcr-Abl gene revealed that SFR and in a lesser degree IM inhibited the expression of the gene, while in contrast CRC induced an increase. The ultimate goal was to evaluate the existence of a potential antitumor activity of saffron's constituents SFR and CRC. (C) 2014 Elsevier Ltd. All rights reserved.
机译:番红花(番红花L(藏红花)的主要成分)已被发现抑制表达Bcr-Abl蛋白酪氨酸激酶活性的K-562人慢性骨髓性白血病(CML)细胞的生长。我们研究的目的是利用计算机方法研究生物活性藏红花成分藏红花红素(CRC)和sa(SFR)抑制Bcr-Abl蛋白活性的能力,以及这些化合物的体外作用。对Bcr-Abl的K-562生长和基因表达的影响在硅胶分子对接研究中发现,大多数SFR可以与Bcr-Abl蛋白连接,该蛋白与治疗CML的药物甲磺酸伊马替尼(IM)位于同一位置,位于蛋白的结合腔内。预测的极性相互作用和在活性位点内部构成疏水腔的疏水接触说明了观察到的抑制活性。细胞毒性实验表明SFR和CRC介导了对K562细胞的细胞毒性反应。对Bcr-Abl基因表达的体外研究表明,SFR和较小程度的IM抑制了该基因的表达,而CRC则诱导了这种表达的增加。最终目的是评估藏红花成分SFR和CRC的潜在抗肿瘤活性。 (C)2014 Elsevier Ltd.保留所有权利。

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