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首页> 外文期刊>Anti-cancer drugs >Isoflavone lupiwighteone induces cytotoxic, apoptotic, and antiangiogenic activities in DU-145 prostate cancer cells
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Isoflavone lupiwighteone induces cytotoxic, apoptotic, and antiangiogenic activities in DU-145 prostate cancer cells

机译:异黄酮黄皮维酮在DU-145前列腺癌细胞中诱导细胞毒性,凋亡和抗血管生成活性

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摘要

Isoflavones constitute a large series of compounds found in many plants. They make up an important part of the diet and have a broad spectrum of biological activities such as cytotoxic and antitumor effects. Lupiwighteone (Lup) is an isoflavone-type compound. It is distributed widely in wild-growing plants such as Glycyrrhiza glabra, Lupinus, and Lotus pedunculatus. On the basis of existing research, Lup shows antioxidant and antimicrobial effects, but its antitumor activity has not been reported as yet. This study aimed to examine the antitumor activity of Lup, explore its antitumor mechanism in a human prostate carcinoma cell line (DU-145), and evaluate its antiangiogenetic activity in the human umbilical vein endothelial cell line (HUVEC). The results showed that Lup could inhibit the growth of DU-145 and HUVEC cells in a concentration-dependent and time-dependent manner by a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay. Flow cytometry analysis indicated that Lup could induce cell cycle arrest, cells apoptosis, mitochondrial membrane potential loss, and an increase in intracellular reactive oxygen species of DU-145 cells. Upregulation of Bax, cytochrome c, caspase-3, and PARP-1 protein expressions and downregulation of Bcl-2, procaspase-9, and p-Akt protein expressions were observed by western blot after the treatment of Lup. Furthermore, the effects of Lup on the cellular behavior of HUVECs were also investigated. Altogether, our data proved the anticancer and antiangiogenesis potential of Lup. Copyright (C) 2015 Wolters Kluwer Health, Inc. All rights reserved.
机译:异黄酮构成许多植物中发现的大量化合物。它们构成饮食的重要组成部分,并具有广泛的生物学活性,例如细胞毒性和抗肿瘤作用。 Lupiwighteone(Lup)是异黄酮类化合物。它广泛分布在野生植物中,如甘草,羽扇豆和荷叶pedunculatus。在现有研究的基础上,Lup具有抗氧化和抗菌作用,但其抗肿瘤活性尚未见报道。这项研究旨在检查Lup的抗肿瘤活性,探索其在人前列腺癌细胞系(DU-145)中的抗肿瘤机制,并评估其在人脐静脉内皮细胞系(HUVEC)中的抗血管生成活性。结果表明,Lup可以通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑测定以浓度依赖性和时间依赖性抑制DU-145和HUVEC细胞的生长。 。流式细胞仪分析表明,Lup可以诱导DU-145细胞的细胞周期停滞,细胞凋亡,线粒体膜电位损失以及细胞内活性氧的增加。 Lup处理后,通过蛋白质印迹观察到Bax,细胞色素c,caspase-3和PARP-1蛋白表达上调,而Bcl-2,procaspase-9和p-Akt蛋白表达下调。此外,还研究了Lup对HUVEC细胞行为的影响。总之,我们的数据证明了Lup的抗癌和抗血管生成潜力。版权所有(C)2015 Wolters Kluwer Health,Inc.保留所有权利。

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