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Anticancer Effect of Nemopilema nomurai Jellyfish Venom on HepG2 Cells and a Tumor Xenograft Animal Model

机译:Nemopilema nomurai水母毒液对HepG2细胞和肿瘤异种移植动物模型的抗癌作用

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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:为了潜在的治疗应用,已经对各种动物毒液及其成分进行了广泛的研究。这项研究评估了Nemopilema nomurai水母毒液(NnV)是否具有抗癌活性。 NnV通过凋亡细胞死亡强烈诱导HepG2细胞的细胞毒性,如颜色形态的改变,procaspase-3的激活和Bax / Bcl-2比的增加所证明。此外,NnV抑制PI3K,PDK1,Akt,mTOR,p70S6K和4EBP1的磷酸化,而增强p-PTEN的表达。有趣的是,NnV也使与Akt激活相关的负反馈回路失活,如在Ser473处的Akt和在Ser2481处的mTOR下调所证明的。 NnV的抗癌作用在HepG2异种移植小鼠模型中很明显,没有明显的毒性。 NnV对HepG2细胞的死亡被金属蛋白酶抑制剂四环素抑制,这表明NnV中的金属蛋白酶成分与抗癌作用密切相关。这项研究首次证明,NnV通过双重抑制Akt和mTOR信号通路在HepG2细胞中发挥高度选择性的细胞毒性,而在正常细胞中则没有。

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