...
首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Chemical markers' knockout coupled with UHPLC-HRMS-based metabolomics reveals anti-cancer integration effects of the curcuminoids of turmeric (Curcuma longa L.) on lung cancer cell line
【24h】

Chemical markers' knockout coupled with UHPLC-HRMS-based metabolomics reveals anti-cancer integration effects of the curcuminoids of turmeric (Curcuma longa L.) on lung cancer cell line

机译:化学标志物'敲除与基于UHPLC-HRMS的代谢组学揭示姜黄(Curcuma Longa L.)姜黄素对肺癌细胞系的抗癌酰胺效果

获取原文
获取原文并翻译 | 示例
           

摘要

Turmeric (Curcuma longa L, Zingiberaceae) rhizomes exhibit versatile biological activities including the significant anti-cancer property. As an herbal medicine, the therapeutic effects of turmeric may be expressed by multi-components which have complicated integration effects on multi-targets. Therefore, having previously found three A549 cell-binding curcuminoids (curcumin, Cur; demethoxycurcumin, DMcur; bisdemethoxycurcumin, BMcur) from turmeric, studies were undertaken in this paper to determine the anti-cancer mechanism and integration effects of these curcuminoids by using chemical markers' knockout and UHPLC-LTQOrbitrap MS-based metabolomics. Four curcuminoid-containing fractions including a mixture of 3 cell-binding curcuminoids (CE), and three individual curcuminoids with natural proportion in turmeric were prepared by chemical markers' knockout method. CE, Cur, DMcur and BMcur fractions showed significant anti-cancer activity on A549 cells. The activities of CE, Cur and BMcur fractions were comparative with the turmeric crude extract (TcE). In the metabolomics study, CE and three individual curcuminoid fractions changed the expression of 25 metabolites in A549 cells, which were involved in glycerophospholipid catabolism, sphingolipid metabolism and fatty acid metabolism, etc. Among them, glycerophospholipid catabolism was disordered greatly in CE group, while sphingolipid metabolism was suggested to be closely related to DMcur and BMcur activity. Furthermore, the metabolomics data showed that three curcuminoids existed synergistic and antagonistic actions and the use of multi-curcuminoids is more powerful than use of single curcuminoid on the metabolic alterations of A549 cells. (C) 2019 Elsevier B.V. All rights reserved.
机译:姜黄(Curcuma Longa L,Zingiberaceae)根茎表现出多功能的生物活性,包括显着的抗癌性能。作为草药,姜黄的治疗效果可以通过多组分表达,这对多目标具有复杂的整合效应。因此,先前发现了三种A549细胞结合姜黄素(姜黄素,Cur; Demethoxycurcumin,DMCur;双甲氧基尿蛋白,BMCUR)在本文中进行了研究,以确定通过使用化学标记的抗癌机制和这些姜黄素的整合效应'基于敲除和UHPLC-LTQITRAP MS的代谢组。通过化学标记物的敲除法制制备包括3个细胞结合姜黄素(Ce)的混合物的含四种含丁烷的含量,以及具有自然比例的三种单独的姜黄素。 CE,Ce,DMCur和BMCur级分在A549细胞上显示出显着的抗癌活性。 Ce,Cre和Bmcur级分的活性与姜黄粗提物(TCE)对比。在代谢组科研究中,Ce和三种单独的姜黄素级分在A549细胞中改变了25个代谢物的表达,其参与甘油磷脂分解代谢,鞘脂代谢和脂肪酸代谢等,在CE组中甘油磷脂分解代谢大大紊乱。提出鞘脂代谢与DMCUR和BMCUR活动密切相关。此外,代谢组合数据显示,存在三种姜黄素的协同和拮抗作用,并且使用多姜黄素的使用比使用单仙姜黄素的使用更强大于A549细胞的代谢改变。 (c)2019 Elsevier B.v.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号