Suppr超能文献

金纳米粒子通过与反义寡核苷酸和 AS1411 适体功能化来抑制 MCF-7 乳腺癌细胞系中的 miR-155。

Inhibition of miR-155 in MCF-7 breast cancer cell line by gold nanoparticles functionalized with antagomir and AS1411 aptamer.

机构信息

Department of Medical Biotechnology, School of Advanced Technologies, Shahrekord University of Medical Sciences, Shahrekord, Iran.

Clinical Biochemistry Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.

出版信息

J Cell Physiol. 2020 Oct;235(10):6887-6895. doi: 10.1002/jcp.29584. Epub 2020 Jan 31.

Abstract

MicroRNAs are key factors for many biological functions. These regulatory molecules affect various gene networks and involve the subsequent signaling pathways. Therefore, disrupting the expression of these molecules is associated with multiple anomalies in the cells and body. One of the most important related abnormalities is the incidence of cancer. Thus, targeting microRNAs (miRNAs) is an effective approach for cancer gene therapy. Various factors are used for this purpose, including the antagomir nucleotide structure. There are some obstacles in the delivery of nucleotide therapeutics to the target cells, however, the use of nanoparticles could partly overcome these defeciencies. On the other hand, targeted delivery of antagomirs using aptamers, reduces nonspecific effects on nontarget cells. Considering the above, in this study, we designed and fabricated a nanocarrier composed of gold nanoparticles (GNPs), antagomir-155, and nucleolin specific aptamer for breast cancer study and therapy. Here, GNPs were synthesized using citrate reduction and were modified by polyA sequences, AS1411 aptamer, and antagomir-155. Attachment of molecules were confirmed using gel electrophoresis, atomic force microscopy imaging and electrochemical test. The specific entry of modified nanoparticles was investigated by fluorescence microscopy. The efficacy of modified nanoparticles was evaluated using a quantitative polymerase chain reaction (q-PCR) for miR-155 and its target gene. Efficient and specific delivery of AuNP-Apt-anti-miR-155 to target cells was confirmed in comparison with the control cell. The q-PCR analysis showed not only a significant decrease in mir-155 levels but also an elevated TP53INP1 mRNA, direct target of miR-155. The proposed structure inhibits proliferation and stimulates apoptosis by increasing the expression of TP53INP1. Our results suggest that AuNP-Apt-anti-miR-155 could be a promising nano constructor for breast cancer treatment.

摘要

微小 RNA 是许多生物学功能的关键因素。这些调节分子影响各种基因网络,并涉及随后的信号通路。因此,破坏这些分子的表达与细胞和体内的多种异常有关。最重要的相关异常之一是癌症的发生。因此,靶向微小 RNA(miRNA)是癌症基因治疗的有效方法。为此目的使用了各种因素,包括反义核苷酸结构。然而,核苷酸治疗剂递送到靶细胞存在一些障碍,使用纳米粒子可以部分克服这些缺陷。另一方面,使用适体靶向递送电针对抗物,减少对非靶细胞的非特异性作用。考虑到上述情况,在这项研究中,我们设计并制造了一种由金纳米粒子(GNPs)、反义寡核苷酸-155 和核仁素特异性适体组成的纳米载体,用于乳腺癌的研究和治疗。这里,通过柠檬酸还原法合成了 GNPs,并通过聚 A 序列、AS1411 适体和反义寡核苷酸-155 进行了修饰。使用凝胶电泳、原子力显微镜成像和电化学测试证实了分子的附着。通过荧光显微镜研究了修饰后的纳米粒子的特异性进入。通过定量聚合酶链反应(q-PCR)评估了 miR-155 及其靶基因修饰纳米粒子的疗效。与对照细胞相比,证实了修饰后的纳米粒子对靶细胞的高效和特异性递送。q-PCR 分析不仅显示 miR-155 水平显著降低,而且直接靶标 miR-155 的 TP53INP1 mRNA 水平升高。所提出的结构通过增加 TP53INP1 的表达来抑制增殖并刺激细胞凋亡。我们的结果表明,AuNP-Apt-anti-miR-155 可能是一种有前途的用于乳腺癌治疗的纳米构建体。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验