• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

利用展示亲和体的生物纳米胶囊和脂质体复合物载体进行 siRNA 递送来靶向癌细胞特异性的 RNA 干扰。

Targeting cancer cell-specific RNA interference by siRNA delivery using a complex carrier of affibody-displaying bio-nanocapsules and liposomes.

机构信息

Department of Chemical Science and Engineering, Graduate School of Engineering, Kobe University, 1-1 Rokkodai, Nada, Kobe 657-8501, Japan.

出版信息

J Nanobiotechnology. 2013 Jun 24;11:19. doi: 10.1186/1477-3155-11-19.

DOI:10.1186/1477-3155-11-19
PMID:23800313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3699380/
Abstract

BACKGROUND

Small interfering RNA (siRNA) has attracted attention in the field of nucleic acid medicine as a RNA interference (RNAi) application that leads to gene silencing due to specific messenger RNA (mRNA) destruction. However, since siRNA is unstable in blood and unable to cross the cell membrane, encapsulation of siRNA into a carrier is required.

RESULTS

In this study, we used a carrier that combined ZHER2-displaying bio-nanocapsule (derived from hepatitis B virus surface antigen) and liposomes in a complex in order to investigate the feasibility of effective and target-cell-specific RNAi applications. As a result, by observing RNAi only in HER2-expressing breast cancer cells, using our proposed methodology, we successfully demonstrated target-cell-specific delivery and effective function expression of siRNA.

CONCLUSIONS

These findings show that, in the field of nucleic acid medicine, ZHER2-BNC/LP can be a useful carrier for siRNA delivery, and could also become a useful tool for gene silencing and to accomplish protein knock-down.

摘要

背景

小干扰 RNA(siRNA)作为一种 RNA 干扰(RNAi)应用,因其能特异性破坏信使 RNA(mRNA)而引起基因沉默,在核酸药物领域引起了关注。然而,由于 siRNA 在血液中不稳定且无法穿透细胞膜,因此需要将其包裹在载体中。

结果

在这项研究中,我们使用了一种载体,将展示 ZHER2 的生物纳米胶囊(源自乙型肝炎病毒表面抗原)与脂质体复合,以研究有效且针对靶细胞的 RNAi 应用的可行性。结果表明,通过仅在 HER2 表达的乳腺癌细胞中观察到 RNAi,我们成功地证明了我们提出的方法可以实现 siRNA 的靶向细胞特异性递送和有效功能表达。

结论

这些发现表明,在核酸药物领域,ZHER2-BNC/LP 可以作为 siRNA 递送的有用载体,也可以成为基因沉默和实现蛋白敲低的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/64fdbe097801/1477-3155-11-19-8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/e4157b0d6f3d/1477-3155-11-19-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/015125bbe68b/1477-3155-11-19-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/bdb7b99bb917/1477-3155-11-19-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/fa4305f304bb/1477-3155-11-19-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/8f9084c528c6/1477-3155-11-19-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/dac7abcb2bc2/1477-3155-11-19-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/1779869a86da/1477-3155-11-19-7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/64fdbe097801/1477-3155-11-19-8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/e4157b0d6f3d/1477-3155-11-19-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/015125bbe68b/1477-3155-11-19-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/bdb7b99bb917/1477-3155-11-19-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/fa4305f304bb/1477-3155-11-19-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/8f9084c528c6/1477-3155-11-19-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/dac7abcb2bc2/1477-3155-11-19-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/1779869a86da/1477-3155-11-19-7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b4/3699380/64fdbe097801/1477-3155-11-19-8.jpg

相似文献

1
Targeting cancer cell-specific RNA interference by siRNA delivery using a complex carrier of affibody-displaying bio-nanocapsules and liposomes.利用展示亲和体的生物纳米胶囊和脂质体复合物载体进行 siRNA 递送来靶向癌细胞特异性的 RNA 干扰。
J Nanobiotechnology. 2013 Jun 24;11:19. doi: 10.1186/1477-3155-11-19.
2
Complex carriers of affibody-displaying bio-nanocapsules and composition-varied liposomes for HER2-expressing breast cancer cell-specific protein delivery.展示亲和体的生物纳米胶囊的复杂载体和组成变化的脂质体,用于 HER2 表达的乳腺癌细胞特异性蛋白递药。
J Drug Target. 2012 Dec;20(10):897-905. doi: 10.3109/1061186X.2012.725404. Epub 2012 Oct 1.
3
[Bio-nanocapsules for in vivo pinpoint drug delivery].用于体内精准给药的生物纳米胶囊
Yakugaku Zasshi. 2007 May;127(5):797-805. doi: 10.1248/yakushi.127.797.
4
Proof of concept studies for siRNA delivery by nonionic surfactant vesicles: and evaluation of protein knockdown.非离子表面活性剂囊泡介导 siRNA 递送的概念验证研究:和 蛋白质敲低的评价。
J Liposome Res. 2019 Sep;29(3):229-238. doi: 10.1080/08982104.2018.1531424. Epub 2019 Jan 1.
5
Bio-nanocapsule conjugated with liposomes for in vivo pinpoint delivery of various materials.与脂质体结合的生物纳米胶囊用于体内各种物质的精准递送。
J Control Release. 2008 Mar 20;126(3):255-64. doi: 10.1016/j.jconrel.2007.12.002. Epub 2007 Dec 14.
6
Delivery of siRNA into breast cancer cells via phage fusion protein-targeted liposomes.噬菌体融合蛋白靶向脂质体介导的 siRNA 递送至乳腺癌细胞。
Nanomedicine. 2011 Jun;7(3):315-23. doi: 10.1016/j.nano.2010.10.004. Epub 2010 Nov 2.
7
siRNA delivery by a transferrin-associated lipid-based vector: a non-viral strategy to mediate gene silencing.通过转铁蛋白相关脂质载体递送小干扰RNA:一种介导基因沉默的非病毒策略。
J Gene Med. 2007 Mar;9(3):170-83. doi: 10.1002/jgm.1006.
8
Affibody-displaying bionanocapsules for specific drug delivery to HER2-expressing cancer cells.展示结合体的仿生纳米胶囊,可将药物递送至 HER2 表达的癌细胞。
Bioorg Med Chem Lett. 2010 Oct 1;20(19):5726-31. doi: 10.1016/j.bmcl.2010.08.011. Epub 2010 Aug 6.
9
Affibody-displaying bio-nanocapsules effective in EGFR, typical biomarker, expressed in various cancer cells.展示亲和体的生物纳米胶囊对表皮生长因子受体(EGFR,一种在多种癌细胞中表达的典型生物标志物)有效。
Bioorg Med Chem Lett. 2017 Jan 15;27(2):336-341. doi: 10.1016/j.bmcl.2016.11.038. Epub 2016 Nov 15.
10
Nanoparticle-enabled, image-guided treatment planning of target specific RNAi therapeutics in an orthotopic prostate cancer model.基于纳米颗粒的靶向特定 RNAi 治疗的影像引导治疗规划在原位前列腺癌模型中的应用。
Small. 2014 Aug 13;10(15):3072-82. doi: 10.1002/smll.201303842. Epub 2014 Apr 6.

引用本文的文献

1
Artificial Scaffold Polypeptides As an Efficient Tool for the Targeted Delivery of Nanostructures In Vitro and In Vivo.人工支架多肽作为纳米结构在体外和体内靶向递送的有效工具。
Acta Naturae. 2022 Jan-Mar;14(1):54-72. doi: 10.32607/actanaturae.11545.
2
Nanoparticle-mediated targeted drug delivery for breast cancer treatment.纳米颗粒介导的靶向药物递送用于乳腺癌治疗。
Biochim Biophys Acta Rev Cancer. 2019 Apr;1871(2):419-433. doi: 10.1016/j.bbcan.2019.04.006. Epub 2019 Apr 26.
3
Drug delivery approaches for breast cancer.乳腺癌的药物递送方法

本文引用的文献

1
Quantitative silencing of EGFP reporter gene by self-assembled siRNA lipoplexes of LinOS and cholesterol.LinOS 和胆固醇自组装 siRNA 脂质体对 EGFP 报告基因的定量沉默作用。
Mol Pharm. 2012 Nov 5;9(11):3384-95. doi: 10.1021/mp300435x. Epub 2012 Oct 25.
2
Complex carriers of affibody-displaying bio-nanocapsules and composition-varied liposomes for HER2-expressing breast cancer cell-specific protein delivery.展示亲和体的生物纳米胶囊的复杂载体和组成变化的脂质体,用于 HER2 表达的乳腺癌细胞特异性蛋白递药。
J Drug Target. 2012 Dec;20(10):897-905. doi: 10.3109/1061186X.2012.725404. Epub 2012 Oct 1.
3
Nanoparticle-based delivery of small interfering RNA: challenges for cancer therapy.
Int J Nanomedicine. 2017 Aug 24;12:6205-6218. doi: 10.2147/IJN.S140325. eCollection 2017.
4
Effects of AQP5 gene silencing on proliferation, migration and apoptosis of human glioma cells through regulating EGFR/ERK/ p38 MAPK signaling pathway.水通道蛋白5基因沉默通过调节表皮生长因子受体/细胞外信号调节激酶/ p38丝裂原活化蛋白激酶信号通路对人胶质瘤细胞增殖、迁移和凋亡的影响
Oncotarget. 2017 Jun 13;8(24):38444-38455. doi: 10.18632/oncotarget.16461.
5
Phytotoxic Mechanism of Nanoparticles: Destruction of Chloroplasts and Vascular Bundles and Alteration of Nutrient Absorption.纳米颗粒的植物毒性机制:叶绿体和维管束的破坏以及养分吸收的改变。
Sci Rep. 2015 Jun 25;5:11618. doi: 10.1038/srep11618.
6
A display of pH-sensitive fusogenic GALA peptide facilitates endosomal escape from a Bio-nanocapsule via an endocytic uptake pathway.展示 pH 敏感融合 GALA 肽通过内吞摄取途径促进生物纳米胶囊从内涵体中逃逸。
J Nanobiotechnology. 2014 Apr 1;12:11. doi: 10.1186/1477-3155-12-11.
基于纳米颗粒的小干扰 RNA 递呈:癌症治疗的挑战。
Int J Nanomedicine. 2012;7:3637-57. doi: 10.2147/IJN.S23696. Epub 2012 Jul 20.
4
Structural diversity repertoire of gene silencing small interfering RNAs.基因沉默小干扰 RNA 的结构多样性库。
Nucleic Acid Ther. 2011 Jun;21(3):125-31. doi: 10.1089/nat.2011.0286.
5
Insulin-like growth factor-dependent proliferation and survival of triple-negative breast cancer cells: implications for therapy.胰岛素样生长因子依赖性增殖和三阴性乳腺癌细胞的存活:治疗意义。
Neoplasia. 2011 Jun;13(6):504-15. doi: 10.1593/neo.101590.
6
A simple and cost-effective method to transfect small interfering RNAs into pancreatic cancer cell lines using polyethylenimine.使用聚乙烯亚胺将小干扰 RNA 转染入胰腺癌细胞系的简单且经济有效的方法。
Pancreas. 2011 Jan;40(1):144-50. doi: 10.1097/MPA.0b013e3181f7e41c.
7
A multifunctional envelope type nano device (MEND) for gene delivery to tumours based on the EPR effect: a strategy for overcoming the PEG dilemma.基于 EPR 效应的用于肿瘤基因递送的多功能信封型纳米装置(MEND):克服 PEG 困境的策略。
Adv Drug Deliv Rev. 2011 Mar 18;63(3):152-60. doi: 10.1016/j.addr.2010.09.001. Epub 2010 Sep 15.
8
Affibody-displaying bionanocapsules for specific drug delivery to HER2-expressing cancer cells.展示结合体的仿生纳米胶囊,可将药物递送至 HER2 表达的癌细胞。
Bioorg Med Chem Lett. 2010 Oct 1;20(19):5726-31. doi: 10.1016/j.bmcl.2010.08.011. Epub 2010 Aug 6.
9
PEGylation of biodegradable dextran nanogels for siRNA delivery.聚乙二醇化生物可降解葡聚糖纳米胶束用于 siRNA 递送。
Eur J Pharm Sci. 2010 Jul 11;40(4):342-51. doi: 10.1016/j.ejps.2010.04.010. Epub 2010 May 7.
10
Targeted lipoplexes for siRNA delivery.用于小干扰RNA递送的靶向脂质复合物
Methods Enzymol. 2009;465:267-87. doi: 10.1016/S0076-6879(09)65014-X.