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Anti-c-Met antibody bioconjugated with hollow gold nanospheres as a novel nanomaterial for targeted radiation ablation of human cervical cancer cell

机译:抗c-Met抗体与空心金纳米球生物共轭作为一种新型纳米材料可靶向消融人宫颈癌细胞

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摘要

Radiotherapy is preferred to chemotherapy as an adjuvant therapy for postoperative cervical cancer owing to its convenience and minimal effects on various non-targeted systems. The present study sought to investigate whether the utilization of anti-MET proto-oncogene, receptor tyrosine kinase (c-Met) antibodies conjugated to hollow gold nanospheres (anti-c-Met/HGNs) may enhance the efficiency of radiation therapy for cervical cancer. Anti-c-Met/HGNs were synthesized and confirmed to target c-Met, which was overexpressed on the cell membrane of multiple malignancies. The successful synthesis of HGNs was observed using transmission electron microscopy (TEM). Overrepresentation of c-Met in the human cervical cancer cell line CaSki was verified by immunofluorescence. The cellular uptake of HGNs was assessed using inductively coupled plasma atomic emission spectroscopy (ICP-AES). To assess the toxicity of functionalized gold nanospheres, a cell proliferation and toxicity assay was used and flow cytometry, with staining by propidium iodide (PI), was performed to study the cell cycle changes. Each experiment was conducted on three groups: Control, HGNs alone and anti-c-Met/HGNs, with each group also assessed with or without X-rays. The variation of apoptotic rate was observed by flow cytometry using a dual-staining Annexin V-fluorescein isothiocyanate/PI kit. Expression of apoptosis-associated proteins was examined by western blot analysis. TEM revealed a number of hollow spheres with cells with an average diameter of 56.25 nm and a mean wall thickness of 6.56 nm. CaSki cells were detected by inverted fluorescence microscopy via a layer of fluorescent green marker, and ICP-AES confirmed the distinct uptake of anti-c-Met/HGNs by each CaSki cell. Anti-c-Met/HGNs induced 38.7% of cells to stay in the G2/M phase, whereas the equivalent proportion in the control group was 19.8%. Compared with other groups, CaSki cells treated with anti-c-Met/HGNs and 5 Gy X-ray radiation exhibited a higher apoptosis rate (16.92%) and a higher early apoptotic rate (12.30%) compared with cells under other conditions (control+0 Gy: 3.16 and 1.69%; HGN+0 Gy: 3.98 and 1.94%; anti-c-Met/HGN+0 Gy: 3,47 and 1.85%; control+5 Gy: 5.35 and 3.66%; HGN+5 Gy: 7.91 and 4.06%). The anti-c-Met/HGN X-ray-treated group also evidently overexpressed caspase-3 and BCL2 associated X, apoptosis regulator. Anti-c-Met/HGN may, therefore, aid the sensitivity of radiation therapy in cervical cancer.
机译:由于放疗的便利性和对各种非靶向系统的影响极小,因此放疗优于化疗作为术后子宫颈癌的辅助治疗。本研究旨在调查利用抗MET原癌基因受体酪氨酸激酶(c-Met)抗体与空心金纳米球(anti-c-Met / HGNs)偶联是否可提高宫颈癌放射治疗的效率。合成了抗c-Met / HGNs并确认其靶向c-Met,它在多种恶性肿瘤的细胞膜上过表达。使用透射电子显微镜(TEM)观察到HGN的成功合成。通过免疫荧光法证实了c-Met在人宫颈癌细胞系CaSki中的过量表达。使用电感耦合等离子体原子发射光谱法(ICP-AES)评估HGNs的细胞摄取。为了评估功能化金纳米球的毒性,使用了细胞增殖和毒性测定方法,并用碘化丙啶(PI)染色的流式细胞仪研究了细胞周期的变化。每个实验均分为三组:对照组,单独的HGN和抗c-Met / HGN,每组也接受或不接受X射线评估。使用双重染色膜联蛋白V-荧光素异硫氰酸酯/ PI试剂盒通过流式细胞术观察凋亡率的变化。通过蛋白质印迹分析检查凋亡相关蛋白的表达。 TEM显示出许多空心球,其平均直径为56.25nm,平均壁厚为6.56nm。通过倒置荧光显微镜通过一层绿色荧光标记检测CaSki细胞,ICP-AES证实每种CaSki细胞对c-Met / HGNs的摄取不同。抗c-Met / HGNs诱导38.7%的细胞停留在G2 / M期,而对照组的当量比例为19.8%。与其他组相比,经抗c-Met / HGNs和5 Gy X射线处理的CaSki细胞与其他条件下的细胞相比,具有更高的凋亡率(16.92%)和更高的早期凋亡率(12.30%)(对照)。 +0 Gy:3.16和1.69%; HGN + 0 Gy:3.98和1.94%;抗c-Met / HGN + 0 Gy:3.47和1.85%;对照+5 Gy:5.35和3.66%; HGN + 5 Gy:7.91和4.06%)。抗c-Met / HGN X射线治疗组也明显过表达caspase-3和BCL2相关的X凋亡调节剂。因此,抗c-Met / HGN可能有助于宫颈癌放射治疗的敏感性。

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