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Zinc-Doped Copper Oxide Nanocomposites Inhibit the Growth of Pancreatic Cancer by Inducing Autophagy Through AMPK/mTOR Pathway

机译:锌掺杂的氧化铜纳米复合物通过AMPK / mTOR途径诱导自噬抑制胰腺癌的生长。

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摘要

Zinc doped copper oxide nanocomposites (Zn-CuO NPs) is a novel doped metal nanomaterial synthesized by our group using the sonochemical method. Our previous studies have shown that Zn-CuO NPs could inhibit cancer cell proliferation by inducing apoptosis via ROS-mediated pathway. In the present study, we studied the anticancer effect of Zn-CuO NPs on human pancreatic cancer cells. MTS assay revealed that Zn-CuO NPs was able to inhibit cancer cell growth. TEM, flow cytometry and fluorescence microscope analysis showed that Zn-CuO NPs induced autophagy significantly; the number of autophagosomes increased obviously in cells treated with Zn-CuO NPs. Western blot analysis revealed that treatment with the NPs resulted in activation of AMPK/mTOR pathway in both AsPC-1 and MIA Paca-2 cells in dose dependent manners. Moreover, in the presence of AMPK activator AMPKinone, the protein level of p-AMPK, p-ULK1, Beclin-1 and LC3-II/LC3-I increased, while the protein expression of p-AMPK, p-ULK1, Beclin-1 and LC3-II/LC3-I decreased in the presence of AMPK inhibitor Compound C. In vivo study using xenograft mice revealed that Zn-CuO NPs significantly inhibited tumor growth with low toxicity. Our study confirms that Zn-CuO NPs inhibit the tumor growth both in vitro and in vivo for pancreatic cancer. AMPK/mTOR pathway plays an important role in the NPs induced inhibition of tumor growth.
机译:锌掺杂氧化铜纳米复合材料(Zn-CuO NPs)是我们小组采用声化学方法合成的新型掺杂金属纳米材料。我们以前的研究表明,Zn-CuO NPs可以通过ROS介导的途径诱导细胞凋亡来抑制癌细胞的增殖。在本研究中,我们研究了Zn-CuO NPs对人胰腺癌细胞的抗癌作用。 MTS分析表明,Zn-CuO NPs能够抑制癌细胞的生长。透射电镜,流式细胞仪和荧光显微镜分析表明,Zn-CuO NPs显着诱导自噬。 Zn-CuO NPs处理的细胞中自噬体的数量明显增加。蛋白质印迹分析表明,NPs的处理导致AsPC-1和MIA Paca-2细胞中AMPK / mTOR通路以剂量依赖性方式激活。此外,在存在AMPK激活剂AMPKinone的情况下,p-AMPK,p-ULK1,Beclin-1和LC3-II / LC3-I的蛋白质水平增加,而p-AMPK,p-ULK1,Beclin-在AMPK抑制剂化合物C的存在下,图1和LC3-II / LC3-I降低。使用异种移植小鼠的体内研究表明,Zn-CuO NPs以低毒性显着抑制肿瘤生长。我们的研究证实,Zn-CuO NPs在胰腺癌的体内外抑制肿瘤生长。 AMPK / mTOR通路在NPs抑制肿瘤生长中起重要作用。

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