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MnO 纳米片介导的光控 DNA 酶用于细胞内 miRNA 切割以抑制细胞生长。

A MnO nanosheet-mediated photo-controlled DNAzyme for intracellular miRNA cleavage to suppress cell growth.

机构信息

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio-Nanotechnology and Molecular Engineering of Hunan Province, Hunan University, Changsha, P. R. China.

出版信息

Analyst. 2021 May 21;146(10):3391-3398. doi: 10.1039/d1an00406a. Epub 2021 Apr 20.

Abstract

Certain miRNAs, called oncomiRs, play a causal role in the onset and maintenance of cancer when overexpressed, thus, representing a potential new class of targets for therapeutic intervention. RNA-cleaving DNAzymes, mainly aimed at mRNA, have shown potential as therapeutic agents for various diseases. However, it's rarely reported that a DNAzyme was used for intracellular miRNA cleavage to suppress cell growth. Herein, we have developed a MnO nanosheet-mediated photo-controlled DNAzyme (NPD) for intracellular miRNA cleavage to suppress cell growth. MnO nanosheets adsorb photocaged DNAzymes, protect them from enzymatic digestion, and efficiently deliver them into cells. In the presence of intracellular glutathione (GSH), MnO nanosheets are reduced to Mn ions, which serve as cofactors of the 8-17 DNAzyme for miRNA cleavage. Once the DNAzyme is activated by light, it can cyclically cleave endogenous miR-21 inside cells, which would suppress cancer cell migration and invasion, and finally induce cancer cell apoptosis.

摘要

某些 miRNA,称为癌基因 miRNA,在过度表达时在癌症的发生和维持中起因果作用,因此代表了治疗干预的一个新的潜在靶点类别。主要针对 mRNA 的 RNA 切割 DNA 酶已显示出作为各种疾病治疗剂的潜力。然而,很少有报道称 DNA 酶用于细胞内 miRNA 切割以抑制细胞生长。在这里,我们开发了一种基于 MnO 纳米片的光控 DNA 酶 (NPD) 用于细胞内 miRNA 切割以抑制细胞生长。MnO 纳米片吸附光封闭 DNA 酶,防止它们被酶消化,并将其有效地递送到细胞内。在细胞内谷胱甘肽 (GSH) 的存在下,MnO 纳米片被还原为 Mn 离子,Mn 离子作为 8-17 DNA 酶切割 miRNA 的辅助因子。一旦 DNA 酶被光激活,它就可以在细胞内循环切割内源性 miR-21,从而抑制癌细胞迁移和侵袭,最终诱导癌细胞凋亡。

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