Liu Jiao, Liang Ying, Liu Ting, Li Dengke, Yang Xingsheng
Department of Gynecology and Obstetrics, Qilu Hospital, Shandong University, Wenhuaxilu No. 107, Jinan, 250012 Shandong Province China.
Department of General Surgery, Qilu Hospital, Shandong University, Wenhuaxilu No. 107, Jinan, 250012 Shandong Province China.
Nanoscale Res Lett. 2015 May 15;10:218. doi: 10.1186/s11671-015-0923-2. eCollection 2015.
The study aimed to confirm that anti-epidermal growth factor receptor (EGFR) monoclonal antibody-conjugated hollow gold nanospheres (anti-EGFR/HGNs) can be selectively uptaken by cervical cancer cells and induce its apoptosis when combined with radiotherapy, as a result enhancing radiosensitivity of cervical cancer cells. HGNs with a mean diameter of 54.6 ± 7.11 nm and wall thickness of 5.01 ± 2.23 nm were viewed by transmission electron microscopy (TEM). Cell uptake was assayed by inductively coupled plasma atomic emission spectroscopy (ICP-AES). The cytotoxicity on HeLa cells, which were used in our experiment, was assessed by CCK-8 assay. Cell cycle and apoptosis were examined by an Annexin V-FITC/propidium iodide (PI) kit with flow cytometry (FCM). The expression of several critical apoptosis-related proteins, including Bcl-2, Bax, Bad, and active caspase 3, was tested by western blot analysis. Cells treated by anti-EGFR/HGNs showed an obvious increase in nanoparticle uptake compared to naked HGNs. Anti-EGFR/HGNs combined with radiation resulted in a significant growth inhibition, compared with radiation combined with naked HGNs. Anti-EGFR/HGNs remarkably increased the ratio of HeLa cells in the G2/M phase and induced more apoptosis by an obvious deregulation of Bcl-2 and upregulation of Bax, Bad, and caspase 3 when combined with radiation. Therefore, anti-EGFR/HGNs can increase the targeted uptake of HGNs by HeLa cells and enhance radiocytotoxic targeting of cervical cancer at megavoltage radiation energies.
该研究旨在证实抗表皮生长因子受体(EGFR)单克隆抗体偶联的中空金纳米球(抗EGFR/HGNs)可被宫颈癌细胞选择性摄取,并在与放射治疗联合时诱导其凋亡,从而提高宫颈癌细胞的放射敏感性。通过透射电子显微镜(TEM)观察到平均直径为54.6±7.11nm、壁厚为5.01±2.23nm的HGNs。通过电感耦合等离子体原子发射光谱法(ICP-AES)测定细胞摄取情况。通过CCK-8法评估对我们实验中使用的HeLa细胞的细胞毒性。通过Annexin V-FITC/碘化丙啶(PI)试剂盒和流式细胞术(FCM)检测细胞周期和凋亡情况。通过蛋白质免疫印迹分析检测包括Bcl-2、Bax、Bad和活性半胱天冬酶3在内的几种关键凋亡相关蛋白的表达。与裸HGNs相比,经抗EGFR/HGNs处理的细胞纳米颗粒摄取明显增加。与放射联合裸HGNs相比,抗EGFR/HGNs联合放射导致显著的生长抑制。抗EGFR/HGNs与放射联合时,显著增加了HeLa细胞在G2/M期的比例,并通过明显下调Bcl-2以及上调Bax、Bad和半胱天冬酶3诱导更多凋亡。因此,抗EGFR/HGNs可增加HeLa细胞对HGNs的靶向摄取,并在兆伏级辐射能量下增强宫颈癌的放射细胞毒性靶向作用。