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MnO 纳米片用于 A549 细胞化学动力学治疗的作用机制。

Mechanism underlying the effect of MnO nanosheets for A549 cell chemodynamic therapy.

机构信息

Guangxi Key Laboratory of Information Materials, School of Materials Science and Engineering, Guilin University of Electronic Technology, Guilin, 541004, China.

State Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmacy Sciences, Guangxi Normal University, Guilin, 541004, China.

出版信息

Mikrochim Acta. 2023 Sep 11;190(10):381. doi: 10.1007/s00604-023-05974-x.

Abstract

MnO nanosheets (MnONSs) were synthesized by one-step method, and MnONSs were applied to A549 cell chemodynamic Therapy (CDT). The cytotoxicity, redox ability, and reactive oxygen species production of MnONSs have been investigated, and differences in cell metabolism during CDT were determined using liquid chromatography-mass spectrometry (LC-MS/MS). In addition, the metabolites of A549 lung cancer cells affected by MnONSs treatment are identified; metabolite differences were identified by PCA, PLS-DA, orthogonal PLS-DA, and other methods; and these differences were analyzed using non-targeted metabolomics. We found that A549 cells which were treated by MnONSs have 17 different metabolites and 9 metabolic pathways that varied markedly. Owing to their unique composition, structure, and physicochemical properties, MnONSs and their composites have become a favored type of nanomaterial used for CDT in cancer therapy. This work provides insights into the mechanism underlying the effects of MnONSs on the tumor microenvironment of A549 lung cancer cells, effectively making up for the deficiency of the study on cellular mechanism of CDT-induced apoptosis of cancer cells. It could aid the development of cancer CDT treatment strategies and help improve the use of nanomaterials in the clinical field.

摘要

通过一步法合成了 MnO 纳米片(MnONSs),并将其应用于 A549 细胞化学动力学治疗(CDT)。研究了 MnONSs 的细胞毒性、氧化还原能力和活性氧的产生,并通过液相色谱-质谱联用(LC-MS/MS)确定了 CDT 过程中细胞代谢的差异。此外,还鉴定了受 MnONSs 处理影响的 A549 肺癌细胞的代谢物;通过 PCA、PLS-DA、正交 PLS-DA 等方法鉴定了代谢物差异,并通过非靶向代谢组学对这些差异进行了分析。结果发现,用 MnONSs 处理的 A549 细胞有 17 种不同的代谢物和 9 种明显变化的代谢途径。由于其独特的组成、结构和物理化学性质,MnO2 纳米片及其复合材料已成为癌症治疗中 CDT 中使用的首选纳米材料类型。这项工作深入了解了 MnONSs 对 A549 肺癌细胞肿瘤微环境的影响机制,有效地弥补了对癌症细胞 CDT 诱导凋亡的细胞机制研究的不足。它可以帮助开发癌症 CDT 治疗策略,并有助于提高纳米材料在临床领域的应用。

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