首页> 美国卫生研究院文献>other >Natural Plants Compounds as Modulators of Epithelial-to-Mesenchymal Transition
【2h】

Natural Plants Compounds as Modulators of Epithelial-to-Mesenchymal Transition

机译:天然植物化合物作为上皮向间充质转化的调节剂

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Epithelial-to-mesenchymal transition (EMT) is a self-regulated physiological process required for tissue repair that, in non-controled conditions may lead to fibrosis, angiogenesis, loss of normal organ function or cancer. Although several molecular pathways involved in EMT regulation have been described, this process does not have any specific treatment. This article introduces a systematic review of effective natural plant compounds and their extract that modulates the pathological EMT or its deleterious effects, through acting on different cellular signal transduction pathways both in vivo and in vitro. Thereby, cryptotanshinone, resveratrol, oxymatrine, ligustrazine, osthole, codonolactone, betanin, tannic acid, gentiopicroside, curcumin, genistein, paeoniflorin, gambogic acid and Cinnamomum cassia extracts inhibit EMT acting on transforming growth factor-β (TGF-β)/Smads signaling pathways. Gedunin, carnosol, celastrol, black rice anthocyanins, Duchesnea indica, cordycepin and Celastrus orbiculatus extract downregulate vimectin, fibronectin and N-cadherin. Sulforaphane, luteolin, celastrol, curcumin, arctigenin inhibit β-catenin signaling pathways. Salvianolic acid-A and plumbagin block oxidative stress, while honokiol, gallic acid, piperlongumine, brusatol and paeoniflorin inhibit EMT transcription factors such as SNAIL, TWIST and ZEB. Plectranthoic acid, resveratrol, genistein, baicalin, polyphyllin I, cairicoside E, luteolin, berberine, nimbolide, curcumin, withaferin-A, jatrophone, ginsenoside-Rb1, honokiol, parthenolide, phoyunnanin-E, epicatechin-3-gallate, gigantol, eupatolide, baicalin and baicalein and nitidine chloride inhibit EMT acting on other signaling pathways (SIRT1, p38 MAPK, NFAT1, SMAD, IL-6, STAT3, AQP5, notch 1, PI3K/Akt, Wnt/β-catenin, NF-κB, FAK/AKT, Hh). Despite the huge amount of preclinical data regarding EMT modulation by the natural compounds of plant, clinical translation is poor. Additionally, this review highlights some relevant examples of clinical trials using natural plant compounds to modulate EMT and its deleterious effects. Overall, this opens up new therapeutic alternatives in cancer, inflammatory and fibrosing diseases through the control of EMT process.
机译:上皮-间充质转变(EMT)是组织修复所需的自我调节的生理过程,在不受控制的情况下,可能导致纤维化,血管生成,正常器官功能丧失或癌症。尽管已描述了涉及EMT调节的几种分子途径,但该过程没有任何特定的处理方法。本文介绍了有效的天然植物化合物及其提取物的系统综述,该化合物通过在体内和体外作用于不同的细胞信号转导途径来调节病理性EMT或其有害作用。因此,隐丹参酮,白藜芦醇,氧化苦参碱,川li嗪,蛇床子素,香豆内酯,甜菜碱,单宁酸,龙胆苦味苦苷,姜黄素,染料木黄酮,pa药苷,藤黄酸和肉桂肉桂提取物抑制EMT作用于转化生长因子-β(TGF-β)。途径。葛根素,香诺酚,celastrol,黑米花色苷,印度洋Du草,虫草素和orbitulatus提取物下调vimectin,纤连蛋白和N-cadherin。萝卜硫素,木犀草素,celastrol,姜黄素,artigeninin抑制β-catenin信号通路。丹酚酸-A和羽扇豆蛋白可阻断氧化应激,而厚朴酚,没食子酸,哌隆明碱,鼠李糖醇和pa药苷可抑制EMT转录因子,如SNAIL,TWIST和ZEB。偏花酸,白藜芦醇,染料木黄酮,黄ical苷,多叶绿素I,Cairicoside E,木犀草素,小ber碱,nimbolide,姜黄素,withferin-A,Jatrophone,人参皂苷Rb1,厚朴酚,单性酚,膦南宁E,表儿茶素-3-没食子酸酯,黄ical苷和黄ical苷和尼替丁氯化物抑制EMT作用于其他信号通路(SIRT1,p38 MAPK,NFAT1,SMAD,IL-6,STAT3,AQP5,缺口1,PI3K / Akt,Wnt /β-catenin,NF-κB,FAK / AKT,Hh)。尽管有大量有关植物天然化合物对EMT进行调节的临床前数据,但临床翻译效果不佳。此外,本综述重点介绍了使用天然植物化合物调节EMT及其有害作用的临床试验的一些相关实例。总体而言,这通过控制EMT过程为癌症,炎症和纤维化疾病开辟了新的治疗选择。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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