> Vestitol and neovestitol are bioactive isoflavonoids isolated from Brazilian red propolis, a unique Apis melif'/> Isoflavonoids from Brazilian red propolis down‐regulate the expression of cancer‐related target proteins: A pharmacogenomic analysis
首页> 外文期刊>Phytotherapy research: PTR >Isoflavonoids from Brazilian red propolis down‐regulate the expression of cancer‐related target proteins: A pharmacogenomic analysis
【24h】

Isoflavonoids from Brazilian red propolis down‐regulate the expression of cancer‐related target proteins: A pharmacogenomic analysis

机译:来自巴西红色蜂胶的异黄酮降低调节癌症相关靶蛋白的表达:药物替代科学分析

获取原文
获取原文并翻译 | 示例
           

摘要

> Vestitol and neovestitol are bioactive isoflavonoids isolated from Brazilian red propolis, a unique Apis melifera type of propolis botanically originated from Dalbergia ecastophyllum . Although these molecules have relevant biological effects, including anticancer and immunomodulatory activities, their mechanism(s) of action and the affected pathways remain largely unknown. Here, we carried out a pharmacogenomic analysis to investigate the effects of vestitol and neovestitol on the whole‐genome expression in human tumor cells, particularly cancer‐related target proteins. HeLa cells were exposed to the compounds at IC 20 and genomic information of treated cells was analyzed using the Illumina transcriptome system and GeneGo MetaCore software. Our results showed that vestitol (IC 20 ?=?214.7?μM) reduced the expression of genes enrolled with the alpha tubulin (fold ?3.7), tubulin in microtubules (fold ?3.7), and histone h3 (fold?=??3.03), and that treatment with neovestitol (IC 20 ?=?102.91?μM) downregulated prostaglandin E synthase gene (fold?=??3.12), which are considered ideal targets for anticancer therapy. These data open avenues for the study of vestitol and neovestitol as potential promising candidates for anticancer therapy. Toxicological, non‐clinical, and clinical validation of the findings presented herein is needed.
机译: >甲酚和新福酚是从巴西红色蜂胶中孤立的生物活性异黄酮,一个独特的< Fi> Apis Melifera 蜂胶类型植物学源自达伯利亚eCastophyllum 。虽然这些分子具有相关的生物学作用,但包括抗癌和免疫调节活动,它们的作用机制和受影响的途径仍然很大程度上。在这里,我们进行了药物替代学分析,以研究留意醇和尼福佐醇对人肿瘤细胞,特别是癌症相关靶蛋白的全基因组表达的影响。使用Illumina转录组系统和Genego Metacore软件将HeLa细胞暴露于IC 20 的化合物中,并分析处理细胞的基因组信息。我们的结果表明,留意醇(IC 20 Δ=Δ214.7?μm)降低了用α微管蛋白(折叠α3.7),微管中的小管蛋白(折叠α3.7)和组蛋白H3 (折叠?= ?? 3.03),用新福酚(IC 20 Δ=α102.91≤μm)下调前列腺素E合酶基因(折叠Δ=Δ2.12),这被认为是理想的目标抗癌治疗。这些数据开放途径,用于研究留意醇和尼福茨基酚作为抗癌治疗的潜在有希望的候选人。需要本文所呈现的结果的毒理学,非临床和临床验证。

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