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自组装氧化锌纳米结构促进癌细胞损伤并抑制胶质母细胞瘤的上皮表型。

Self-Styled ZnO Nanostructures Promotes the Cancer Cell Damage and Supresses the Epithelial Phenotype of Glioblastoma.

作者信息

Wahab Rizwan, Kaushik Neha, Khan Farheen, Kaushik Nagendra Kumar, Choi Eun Ha, Musarrat Javed, Al-Khedhairy Abdulaziz A

机构信息

Zoology department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.

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

出版信息

Sci Rep. 2016 Jan 28;6:19950. doi: 10.1038/srep19950.

Abstract

Extensive researches have been done on the applications of zinc oxide nanoparticles (ZnO-NPs) for the biological purposes. However, the role and toxicity mechanisms of ZnO nanostructures (ZnO-NSts) such as nanoplates (NPls), nanorods (NRs), nanosheets (NSs), nanoflowers (NFs) on cancer cells are not largely known. Present study was focused to investigate the possible mechanisms of apoptosis induced by self-designed ZnO-NSts, prepared at fix pH via solution process and exposed against human T98G gliomas including various cancers and non-malignant embryonic kidney HEK293, MRC5 fibroblast cells. NSts were used for the induction of cell death in malignant human T98G gliomas including various cancers and compared with the non-malignant cells. Notably, NRs were found to induce higher cytotoxicity, inhibitory effects on cancer and normal cells in a dose dependent manner. We also showed that NRs induced cancer cell death through oxidative stress and caspase-dependent pathways. Furthermore, quantitative and qualitative analysis of ZnO-NSts have also been confirmed by statistical analytical parameters such as precision, accuracy, linearity, limits of detection and limit of quantitation. These self-styled NSts could provide new perception in the research of targeted cancer nanotechnology and have potentiality to improve new therapeutic outcomes with poor diagnosis.

摘要

针对氧化锌纳米颗粒(ZnO-NPs)在生物学领域的应用,人们已经开展了广泛的研究。然而,诸如纳米板(NPls)、纳米棒(NRs)、纳米片(NSs)、纳米花(NFs)等氧化锌纳米结构(ZnO-NSts)对癌细胞的作用及毒性机制在很大程度上尚不明确。本研究聚焦于探究通过溶液法在固定pH值下制备的自行设计的ZnO-NSts诱导细胞凋亡的可能机制,并将其作用于包括多种癌症类型的人T98G胶质瘤细胞以及非恶性的胚胎肾HEK293、MRC5成纤维细胞。使用ZnO-NSts诱导包括多种癌症类型的恶性人T98G胶质瘤细胞死亡,并与非恶性细胞进行比较。值得注意的是,发现纳米棒以剂量依赖的方式诱导更高的细胞毒性以及对癌细胞和正常细胞的抑制作用。我们还表明,纳米棒通过氧化应激和半胱天冬酶依赖性途径诱导癌细胞死亡。此外,还通过诸如精密度、准确度、线性度、检测限和定量限等统计分析参数对ZnO-NSts进行了定量和定性分析。这些自行设计的纳米结构可为靶向癌症纳米技术的研究提供新的见解,并有可能改善诊断不佳情况下的新治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032b/4730157/884a0256b296/srep19950-f1.jpg

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