Xu Zhen, Feng Qi, Wang Min, Zhao Huange, Lin Yingying, Zhou Songlin
Key Laboratory of Tropical Translational Medicine of the Ministry of Education and Hainan Provincial Key Laboratory of Tropical Medicine, Hainan Medical University, Haikou, China.
Jiangsu Provincial Key Laboratory of Veterinary Bio-pharmaceutical High-tech Research, Jiangsu Agri-Animal Husbandry Vocational College, Taizhou, China.
Front Oncol. 2020 Oct 20;10:575415. doi: 10.3389/fonc.2020.575415. eCollection 2020.
Biosynthetic silver nanoparticles (AgNPs), specifically formed using medicinal plant extracts, have recently exhibited a remarkable therapeutic effect due to their anticancer potential. Here, we synthesized AgNPs using an aqueous extract of a leaves and evaluated its activity against cervical cancer (CCa) and the related molecular mechanisms. The physiochemical properties of the AgNPs were measured by ultraviolet-visible spectrophotometry, nanometre particle size analyzer and transmission electron microscopy. The AgNPs effects on cell proliferation and apoptosis were investigated through MTT, MTS, and colony formation assay; Hoechst 33258 staining; and flow cytometry. The intracellular ROS and oxidative stress levels were assessed using the appropriate commercial kits. Apoptosis-related protein levels were determined by western blotting. We prepared a series of different sized ginkgo extract synthesized AgNPs (GB-AgNPs), and the smallest mean particle size was 40.2 ± 1.2 nm with low polydispersity (0.091 ± 0.011), zeta potential values showed -34.56 mV. Compared to the controls, the GB-AgNP treatment inhibited the cell proliferation and induced the apoptosis of HeLa and SiHa cells. In addition, GB-AgNP treatment led to markedly increased levels of intracellular ROS, the release of cytochrome c (Cyt C) from mitochondria into the cytosol and the cleavage of caspase -9 and -3 in both CCa cell lines. Moreover, NAC, an ROS scavenger, eliminated the effect of GB-AgNPs on the HeLa and SiHa cells. This study reveals that GB-AgNPs suppresses cancer cell proliferation and induces apoptosis by upregulating intracellular ROS generation and inducing the activation of the caspase-dependent mitochondrial apoptotic pathway in CCa cells. Thus, GB-AgNPs may be a potential alternative drug for CCa therapy.
生物合成银纳米颗粒(AgNPs),特别是使用药用植物提取物特异性形成的,由于其抗癌潜力,最近展现出显著的治疗效果。在此,我们使用一种树叶的水提取物合成了AgNPs,并评估了其对宫颈癌(CCa)的活性及相关分子机制。通过紫外可见分光光度法、纳米粒度分析仪和透射电子显微镜测量了AgNPs的理化性质。通过MTT、MTS和集落形成试验、Hoechst 33258染色以及流式细胞术研究了AgNPs对细胞增殖和凋亡的影响。使用合适的商业试剂盒评估细胞内活性氧(ROS)和氧化应激水平。通过蛋白质免疫印迹法测定凋亡相关蛋白水平。我们制备了一系列不同尺寸的银杏提取物合成的AgNPs(GB-AgNPs),最小平均粒径为40.2±1.2 nm,多分散性低(0.091±0.011),zeta电位值为-34.56 mV。与对照组相比,GB-AgNP处理抑制了HeLa和SiHa细胞的增殖并诱导了其凋亡。此外,GB-AgNP处理导致两种CCa细胞系中细胞内ROS水平显著升高、细胞色素c(Cyt C)从线粒体释放到细胞质以及caspase -9和-3的裂解。而且,ROS清除剂NAC消除了GB-AgNPs对HeLa和SiHa细胞的作用。本研究表明,GB-AgNPs通过上调细胞内ROS生成并诱导CCa细胞中caspase依赖的线粒体凋亡途径激活来抑制癌细胞增殖并诱导凋亡。因此,GB-AgNPs可能是CCa治疗的一种潜在替代药物。