首页> 美国卫生研究院文献>Frontiers in Pharmacology >Essential Oil Derived From Eupatorium adenophorum Spreng. Mediates Anticancer Effect by Inhibiting STAT3 and AKT Activation to Induce Apoptosis in Hepatocellular Carcinoma
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Essential Oil Derived From Eupatorium adenophorum Spreng. Mediates Anticancer Effect by Inhibiting STAT3 and AKT Activation to Induce Apoptosis in Hepatocellular Carcinoma

机译:紫茎泽兰的精油。通过抑制STAT3和AKT激活来诱导肝癌细胞凋亡来介导抗癌作用。

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摘要

Eupatorium adenophorum Spreng. (EA) is a well-known noxious invasive species. Gas chromatography-mass spectrometry (GC-MS) analysis revealed that the essential oil derived from EA (EAEO) is mainly composed of sesquiterpenes. However, the pharmacological value of EAEO in hepatocellular carcinoma (HCC) remains largely unexplored. Herein, we investigated the anti-HCC activities of EAEO, and explored the potential mechanisms of EAEO-induced apoptosis. An MTT assay showed that EAEO inhibited HCC cell proliferation with little toxicity on normal liver cells. Wound healing and FACS assays revealed that EAEO suppressed HCC cell migration and arrested cell cycle, respectively. Moreover, EAEO promoted in vitro HCC cell apoptosis, and EAEO treatment inhibited HepG2 xenografts growth and enhanced apoptotic nucleus of xenografts in HepG2-bearing nude mice. Mechanistically, EAEO significantly decreased the ratio of Bcl-2/Bax and resulted in the activation of caspase-9 and -3. EAEO also reduced the expression of Grp78, which in turn relieved the inhibition of caspase-12 and -7. Meanwhile, EAEO suppressed the phosphorylation of STAT3 and AKT, indicative of its anti-HCC potential. In summary, we determined that EAEO treatment promoted HCC apoptosis via activation of the apoptotic signaling pathway in mitochondria and endoplasmic reticulum, as well as repressed the activity of STAT3 and AKT in HCC cells.
机译:紫茎泽兰Spreng。 (EA)是一种众所周知的有害入侵物种。气相色谱-质谱(GC-MS)分析表明,衍生自EA(EAEO)的精油主要由倍半萜烯组成。但是,EAEO在肝细胞癌(HCC)中的药理价值尚待探索。在这里,我们调查了EAEO的抗HCC活性,并探讨了EAEO诱导凋亡的潜在机制。 MTT分析表明,EAEO抑制HCC细胞增殖,对正常肝细胞几乎没有毒性。伤口愈合和FACS分析表明,EAEO分别抑制HCC细胞迁移和阻滞细胞周期。此外,EAEO促进了体外HCC细胞凋亡,并且EAEO处理抑制了携带HepG2的裸鼠体内HepG2异种移植物的生长并增强了异种移植物的凋亡核。从机理上讲,EAEO显着降低了Bcl-2 / Bax的比例,并导致了caspase-9和-3的活化。 EAEO还降低了Grp78的表达,从而减轻了对caspase-12和-7的抑制。同时,EAEO抑制了STAT3和AKT的磷酸化,表明其具有抗HCC的潜力。总之,我们确定EAEO处理通过激活线粒体和内质网中的凋亡信号通路来促进HCC细胞凋亡,并抑制HCC细胞中STAT3和AKT的活性。

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