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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Anticancer Effect of Nemopilema nomurai Jellyfish Venom on HepG2 Cells and a Tumor Xenograft Animal Model
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Anticancer Effect of Nemopilema nomurai Jellyfish Venom on HepG2 Cells and a Tumor Xenograft Animal Model

机译:Nemopilema野生水母毒液对HepG2细胞的抗癌作用及肿瘤异种移植动物模型

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摘要

Various kinds of animal venoms and their components have been widely studied for potential therapeutic applications. This study evaluated whether Nemopilema nomurai jellyfish venom(NnV) has anticancer activity. NnV strongly induced cytotoxicity of HepG2 cells through apoptotic cell death, as demonstrated by alterations of chromatic morphology, activation of procaspase-3, and an increase in the Bax/Bcl-2 ratio. Furthermore, NnV inhibited the phosphorylation of PI3K, PDK1, Akt, mTOR, p70S6K, and 4EBP1, whereas it enhanced the expression of p-PTEN. Interestingly, NnV also inactivated the negative feedback loops associated with Akt activation, as demonstrated by downregulation of Akt at Ser473 and mTOR at Ser2481. The anticancer effect of NnV was significant in a HepG2 xenograft mouse model, with no obvious toxicity. HepG2 cell death by NnV was inhibited by tetracycline, metalloprotease inhibitor, suggesting that metalloprotease component in NnV is closely related to the anticancer effects. This study demonstrates, for the first time, that NnV exerts highly selective cytotoxicity in HepG2 cells via dual inhibition of the Akt and mTOR signaling pathways, but not in normal cells.
机译:已经广泛研究了各种动物毒液及其组分用于潜在的治疗应用。本研究评估了Nemopilema野生水母毒液(NNV)是否具有抗癌活动。 NNV通过凋亡细胞死亡强烈地诱导了HepG2细胞的细胞毒性,如色谱形态的改变,促进酶-3的激活,并增加了Bax / Bcl-2比的增加。此外,NNV抑制PI3K,PDK1,AKT,MTOR,P70S6K和4EBP1的磷酸化,而它增强了P-PTEN的表达。有趣的是,NNV还灭活了与AKT激活相关的负反馈回路,如SER2481的SER473和MTOR下调所证明的。 NNV的抗癌效果在HepG2异种移植小鼠模型中显着,没有明显的毒性。通过Tetracycline,金属蛋白酶抑制剂抑制NNV的HepG2细胞死亡,表明NNV中的金属蛋白酶组分与抗癌效果密切相关。本研究首次证明NNV通过对AKT和MTOR信号传导途径的双重抑制,但不在正常细胞中施加高度选择性细胞毒性。

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