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氧化锌纳米颗粒诱导恶性人 T98G 神经胶质瘤、KB 和非恶性 HEK 细胞死亡。

ZnO nanoparticles induces cell death in malignant human T98G gliomas, KB and non-malignant HEK cells.

机构信息

Abdul Rahman Al-Jeraisy Chair for DNA Research, Department of Zoology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia

出版信息

J Biomed Nanotechnol. 2013 Jul;9(7):1181-9. doi: 10.1166/jbn.2013.1652.

Abstract

This paper reports the synthesis and characterization of ZnO nanoparticles prepared by soft chemical process. The nanoparticles of ZnO possess wurtzite hexagonal phase and were used for the induction of cell death in malignant human T98G gliomas, KB epithermoids and HEK normal non-malignant kidney cells. By applying ZnO nanoparticles, the cells exhibit that the nanoparticles are more efficacious on T98G cancer cells, moderately effective on KB cells and least toxic on normal human HEK cells. The results demonstrated that the treatment with ZnO nanoparticles sensitize T98G cells by increasing both the mitotic (linked to cytogenetic damage) and interphase (apoptosis) death. The ZnO nanoparticles behave as genotoxic drugs, since they induce a micronucleus formation in cells. The present study could be helpful in designing more potent anticancer agents for the therapeutic uses.

摘要

本文报道了通过软化学法制备 ZnO 纳米粒子的合成和表征。所制备的 ZnO 纳米粒子具有纤锌矿六方相结构,并被用于诱导恶性人 T98G 神经胶质瘤、KB 表皮样癌细胞和 HEK 正常非恶性肾细胞的细胞死亡。通过施加 ZnO 纳米粒子,细胞显示出纳米粒子对 T98G 癌细胞更有效,对 KB 细胞中度有效,对正常人类 HEK 细胞毒性最小。结果表明,用 ZnO 纳米粒子处理可通过增加有丝分裂(与细胞遗传学损伤相关)和间期间期(细胞凋亡)死亡来敏化 T98G 细胞。这些 ZnO 纳米粒子表现为遗传毒性药物,因为它们在细胞中诱导微核形成。本研究可能有助于设计更有效的抗癌药物用于治疗用途。

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