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用于前列腺癌细胞靶向基因沉默的KUE-小干扰RNA缀合物的合成

Synthesis of KUE-siRNA Conjugates for Prostate Cancer Cell-Targeted Gene Silencing.

作者信息

Yang Chao, Ma Dejun, Lu Liqing, Yang Xing, Xi Zhen

机构信息

Department of Chemical Biology, State Key Laboratory of Elemento-Organic Chemistry, National Engineering Research Center of Pesticide (Tianjin), Nankai University, Tianjin, 300071, P. R. China.

Department of Nuclear Medicine, Peking University First Hospital, Beijing, 100034, P. R. China.

出版信息

Chembiochem. 2021 Oct 1;22(19):2888-2895. doi: 10.1002/cbic.202100243. Epub 2021 Jul 30.

Abstract

The delivery of siRNAs to selectively target cells poses a great challenge in RNAi-based cancer therapy. The lack of suitable cell-targeting methods seriously restricts the advance in delivering siRNAs to extrahepatic tissues. Based on prostate-specific membrane antigen (PSMA)-targeting ligands, we have synthesized a series of lysine-urea-glutamate (KUE)-siRNA conjugates and verified their effective cell uptake and gene silencing properties in prostate cancers. The results indicated that the KUE-siRNA conjugates could selectively enter PSMA LNCaP cells, eventually down-regulating STAT3 expression. Based on post-synthesis modification and receptor-mediated endocytosis, this strategy of constructing ligand-siRNA conjugates might provide a general method of siRNA delivery for cell-targeted gene silencing.

摘要

在基于RNA干扰的癌症治疗中,将小干扰RNA(siRNAs)选择性地递送至靶细胞是一项巨大的挑战。缺乏合适的细胞靶向方法严重限制了向肝外组织递送siRNAs的进展。基于靶向前列腺特异性膜抗原(PSMA)的配体,我们合成了一系列赖氨酸-尿素-谷氨酸(KUE)-siRNA缀合物,并在前列腺癌中验证了它们有效的细胞摄取和基因沉默特性。结果表明,KUE-siRNA缀合物可以选择性地进入PSMA-LNCaP细胞,最终下调信号转导和转录激活因子3(STAT3)的表达。基于合成后修饰和受体介导的内吞作用,这种构建配体-siRNA缀合物的策略可能为细胞靶向基因沉默提供一种通用的siRNA递送方法。

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