Gamal-Eldeen Amira M, Moustafa Dina, El-Daly Sherien M, Abo-Zeid Mona A M, Saleh Samira, Khoobchandani Menka, Katti Kavita, Shukla Ravi, Katti Kattesh V
Cancer Biology and Genetics Laboratory, Centre of Excellence for Advanced Sciences, National Research Centre, Cairo, Egypt; Department of Biochemistry, National Research Centre, Cairo, Egypt.
Department of Pharmacology and Toxicology, Faculty of Pharmacy, October 6 University, 6 October City, Giza, Egypt.
Biomed Pharmacother. 2017 May;89:1045-1054. doi: 10.1016/j.biopha.2017.03.006. Epub 2017 Mar 12.
In our previous work, we have extensively evaluated the physiochemical characteristics of Gum Arabic-encapsulated gold nanoparticles (GA-AuNPs; 15-18nm) and reported their effectiveness in stopping the tumor initiation via inhibiting the pre-neoplastic lesions in liver.
The rationale of this study is to detect the efficiency of using GA-AuNPs in photothermal application as a non-invasive technique against lung tumor. We investigated the cytotoxicity of GA-AuNPs on A549 cells, and then studied their apoptotic, anti-inflammatory, lipid peroxidation and anti-neovascular effect in in vivo model using a chemically-induced lung cancer in mice. The histopathological changes due to GA-AuNPs were investigated.
In the presence of laser irradiation, GA-AuNPs had a considerable cytotoxicity against A549 cells. The treatment of lung tumor-bearing mice with GA-AuNPs followed by laser exposure enhanced the apoptotic pathway and this was obvious from the histopathological investigations and the elevations in cytochrome-c, death receptor 5 and the subsequent upregulation of caspase-3, we also reported a significant reduction in the levels of the inflammatory mediator TNF-α and the angiogenesis inducer VEGF. An induction of lipid peroxidation was also reported upon treatment with either GA or GA-AuNPs.
GA-AuNPs showed no cytotoxicity in the absence of light, however the combination of GA-AuNPs with laser induced cell death in lung tumor tissues with a reduction in the inflammation and angiogenesis together with an elevation in lipid peroxidation, suggesting the potential use of these functionalized nanoparticles as a promising photothermal non-invasive treatment modality.
在我们之前的工作中,我们广泛评估了阿拉伯胶包裹的金纳米颗粒(GA-AuNPs;15 - 18nm)的物理化学特性,并报道了它们通过抑制肝脏中的癌前病变来阻止肿瘤起始的有效性。
本研究的目的是检测GA-AuNPs在光热应用中作为一种针对肺癌的非侵入性技术的效率。我们研究了GA-AuNPs对A549细胞的细胞毒性,然后在使用化学诱导的小鼠肺癌的体内模型中研究了它们的凋亡、抗炎、脂质过氧化和抗血管生成作用。研究了GA-AuNPs引起的组织病理学变化。
在激光照射下,GA-AuNPs对A549细胞具有相当大的细胞毒性。用GA-AuNPs处理荷肺肿瘤小鼠后再进行激光照射增强了凋亡途径,这从组织病理学研究以及细胞色素c、死亡受体5的升高以及随后caspase-3的上调中很明显,我们还报道了炎症介质TNF-α和血管生成诱导剂VEGF水平的显著降低。在用GA或GA-AuNPs处理后也报道了脂质过氧化的诱导。
GA-AuNPs在无光条件下无细胞毒性,然而GA-AuNPs与激光的组合在肺肿瘤组织中诱导细胞死亡,同时炎症和血管生成减少以及脂质过氧化增加,表明这些功能化纳米颗粒作为一种有前景的光热非侵入性治疗方式具有潜在用途。