首页> 美国卫生研究院文献>Cell Death Disease >Nimbolide a neem limonoid inhibits cytoprotective autophagy to activate apoptosis via modulation of the PI3K/Akt/GSK-3β signalling pathway in oral cancer
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Nimbolide a neem limonoid inhibits cytoprotective autophagy to activate apoptosis via modulation of the PI3K/Akt/GSK-3β signalling pathway in oral cancer

机译:Nimbolide一种印em柠檬苦素通过调节PI3K / Akt /GSK-3β信号传导通路抑制细胞保护性自噬激活细胞凋亡

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摘要

Of late, nimbolide, a limonoid from the neem tree (Azadirachta indica) has gained increasing research attention owing to its potent antiproliferative and apoptosis-inducing effects. The present study was designed to investigate the effect of nimbolide on autophagy and the time point at which the phosphorylation status of GSK-3β and PI3K dictate the choice between autophagy and apoptosis in SCC131 and SCC4 oral cancer cells. Additionally, we analysed changes in the expression of proteins involved in autophagy and apoptosis after therapeutic intervention with nimbolide in a hamster model of oral oncogenesis. Furthermore, we also demonstrate changes in the expression of key genes involved in apoptosis and autophagy during the stepwise evolution of hamster and human OSCCs. Nimbolide-induced stereotypical changes in oral cancer cells characteristic of both apoptosis and autophagy. Time-course experiments revealed that nimbolide induces autophagy as an early event and then switches over to apoptosis. Nimbolide negatively regulates PI3K/Akt signalling with consequent increase in p-GSK-3βTyr216, the active form of GSK-3β that inhibits autophagy. Downregulation of HOTAIR, a competing endogenous RNA that sponges miR-126 may be a major contributor to the inactivation of PI3K/Akt/GSK3 signalling by nimbolide. Analysis of key markers of apoptosis and autophagy as well as p-AktSer473 during sequential progression of hamster and human OSCC revealed a gradual evolution to a pro-autophagic and antiapoptotic phenotype that could confer a survival advantage to tumors. In summary, the results of the present study provide insights into the molecular mechanisms by which nimbolide augments apoptosis by overcoming the shielding effects of cytoprotective autophagy through modulation of the phosphorylation status of Akt and GSK-3β as well as the ncRNAs miR-126 and HOTAIR. Development of phytochemicals such as nimbolide that target the complex interaction between proteins and ncRNAs that regulate the autophagy/apoptosis flux is of paramount importance in cancer prevention and therapeutics.
机译:最近,由于其有效的抗增殖和诱导细胞凋亡的作用,印m树中的柠檬苦素类化合物nimbolide受到了越来越多的研究关注。本研究旨在研究尼姆泊利特对自噬的影响以及GSK-3β和PI3K磷酸化状态决定SCC131和SCC4口腔癌细胞自噬与凋亡之间的选择的时间点。此外,我们分析了在口腔癌发生的仓鼠模型中使用nimbolide进行治疗干预后,涉及自噬和凋亡的蛋白质表达的变化。此外,我们还证明了在仓鼠和人类OSCC逐步进化过程中,涉及凋亡和自噬的关键基因表达的变化。尼姆泊利特诱导口腔癌细胞的定型改变,具有凋亡和自噬特征。时程实验表明,尼姆泊利特作为早期事件诱导自噬,然后转变为凋亡。 Nimbolide负调控PI3K / Akt信号传导,从而增加p-GSK-3β Tyr216 ,这是抑制自噬的GSK-3β活性形式。 HOTAIR是海绵miR-126的竞争内源性RNA的下调,可能是nimbolide导致PI3K / Akt / GSK3信号失活的主要因素。在仓鼠和人OSCC连续进展过程中凋亡和自噬以及p-Akt 的关键标志物的分析显示,其逐渐进化为前自噬和抗凋亡表型,可以为肿瘤带来生存优势。总而言之,本研究的结果提供了分子生物学机制的见解,其通过调节Akt和GSK-3β以及ncRNA miR-126和HOTAIR的磷酸化状态克服了细胞保护性自噬的屏蔽作用,从而使nimbolide增强了细胞凋亡。 。靶向蛋白质和调控自噬/凋亡通量的ncRNA之间复杂相互作用的植物化学物质(如nimbolide)在癌症预防和治疗中至关重要。

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