• 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

使用非病毒基因递送系统靶向肿瘤。

Targeting tumors with non-viral gene delivery systems.

作者信息

Ogris Manfred, Wagner Ernst

机构信息

Department of Pharmacy, Ludwig-Maximilians-Universität, München, Butenandtstrasse 5-13, D-81377 Munich, Germany.

出版信息

Drug Discov Today. 2002 Apr 15;7(8):479-85. doi: 10.1016/s1359-6446(02)02243-2.

DOI:10.1016/s1359-6446(02)02243-2
PMID:11965397
Abstract

Targeting therapeutic genes to tumors is an attractive concept in curing malignant diseases. Systemic gene delivery systems are needed for therapeutic applications in which the target cells are not directly accessible, and which can only be reached via the systemic route. Recent developments in the field of non-viral gene delivery have shown that, based on (poly)cationic carrier molecules, DNA can be efficiently targeted to tumors via the bloodstream. Tailor-made synthetic vectors can be used to achieve predominant gene expression in tumor tissue. Therapeutic concepts based, for example, on suicide genes or cytokines, showed encouraging results in preclinical and also in first clinical evaluations.

摘要

将治疗性基因靶向肿瘤是治疗恶性疾病的一个有吸引力的概念。对于那些靶细胞无法直接接触,只能通过全身途径到达的治疗应用,需要全身基因递送系统。非病毒基因递送领域的最新进展表明,基于(聚)阳离子载体分子,DNA可以通过血液循环有效地靶向肿瘤。定制的合成载体可用于在肿瘤组织中实现主要的基因表达。例如,基于自杀基因或细胞因子的治疗概念在临床前和首次临床评估中都显示出令人鼓舞的结果。

相似文献

1
Targeting tumors with non-viral gene delivery systems.使用非病毒基因递送系统靶向肿瘤。
Drug Discov Today. 2002 Apr 15;7(8):479-85. doi: 10.1016/s1359-6446(02)02243-2.
2
Non-viral vectors in cancer gene therapy: principles and progress.癌症基因治疗中的非病毒载体:原理与进展
Anticancer Drugs. 2001 Apr;12(4):275-304. doi: 10.1097/00001813-200104000-00001.
3
Specific targets in tumor tissue for the delivery of therapeutic genes.用于递送治疗性基因的肿瘤组织中的特定靶点。
Curr Med Chem Anticancer Agents. 2005 Mar;5(2):157-71. doi: 10.2174/1568011053174855.
4
Cells as vehicles for cancer gene therapy: the missing link between targeted vectors and systemic delivery?细胞作为癌症基因治疗的载体:靶向载体与全身递送之间缺失的环节?
Hum Gene Ther. 2002 Jul 20;13(11):1263-80. doi: 10.1089/104303402760128504.
5
Gene delivery using temperature-responsive polymeric carriers.使用温度响应性聚合物载体进行基因递送。
Drug Discov Today. 2002 Apr 1;7(7):426-32. doi: 10.1016/s1359-6446(02)02216-x.
6
Nucleic acid therapeutics: concepts for targeted delivery to solid tumors.核酸疗法:靶向递送至实体瘤的概念
Ther Deliv. 2010 Jul;1(1):91-107. doi: 10.4155/tde.10.9.
7
Cell-derived Exosomes as Promising Carriers for Drug Delivery and Targeted Therapy.细胞衍生的外泌体作为有前途的药物传递和靶向治疗载体。
Curr Cancer Drug Targets. 2018;18(4):347-354. doi: 10.2174/1568009617666170710120311.
8
Atelocollagen-mediated siRNA delivery: future promise for therapeutic application.去端胶原蛋白介导的小干扰RNA递送:治疗应用的未来前景
Ther Deliv. 2014 Apr;5(4):369-71. doi: 10.4155/tde.14.8.
9
[Liposomes as non-viral carriers for genetic drugs].
Postepy Hig Med Dosw (Online). 2016 Mar 16;70:200-9. doi: 10.5604/17322693.1197371.
10
[Research progress of gene recombinant mesenchymal stem cells as tumor targeting delivery vehicles].基因重组间充质干细胞作为肿瘤靶向递送载体的研究进展
Yao Xue Xue Bao. 2013 Aug;48(8):1209-20.

引用本文的文献

1
Preparation and characterization of calcium-doped graphene oxide-chitosan Nanocarrier to enhance the gene delivery in MCF-7 cell line.制备并表征钙掺杂氧化石墨烯-壳聚糖纳米载体以增强 MCF-7 细胞系中的基因传递。
Sci Rep. 2024 Nov 10;14(1):27434. doi: 10.1038/s41598-024-78958-3.
2
Optimizing Active Tumor Targeting Biocompatible Polymers for Efficient Systemic Delivery of Adenovirus.优化主动靶向肿瘤的生物相容性聚合物以实现腺病毒的高效系统递送。
Cells. 2021 Jul 26;10(8):1896. doi: 10.3390/cells10081896.
3
Polymeric vehicles for nucleic acid delivery.
核酸递送用聚合物载体。
Adv Drug Deliv Rev. 2020;156:119-132. doi: 10.1016/j.addr.2020.06.014. Epub 2020 Jun 23.
4
Non-Viral in Vitro Gene Delivery: It is Now Time to Set the Bar!非病毒体外基因递送:现在是提高标准的时候了!
Pharmaceutics. 2020 Feb 21;12(2):183. doi: 10.3390/pharmaceutics12020183.
5
Targeted nonviral gene therapy in prostate cancer.前列腺癌的靶向非病毒基因治疗。
Int J Nanomedicine. 2018 Sep 25;13:5753-5767. doi: 10.2147/IJN.S139080. eCollection 2018.
6
Barriers to Liposomal Gene Delivery: from Application Site to the Target.脂质体基因递送的障碍:从应用部位到靶点
Iran J Pharm Res. 2016 Winter;15(Suppl):3-17.
7
Combined Local Pulmonary and Systemic Delivery of AT2R Gene by Modified TAT Peptide Nanoparticles Attenuates Both Murine and Human Lung Carcinoma Xenografts in Mice.经修饰的TAT肽纳米颗粒联合局部肺和全身递送AT2R基因可减轻小鼠中鼠源和人源肺癌异种移植瘤。
J Pharm Sci. 2017 Jan;106(1):385-394. doi: 10.1016/j.xphs.2016.08.023. Epub 2016 Oct 18.
8
Building Cell Selectivity into CPP-Mediated Strategies.将细胞选择性融入细胞穿透肽介导的策略中。
Pharmaceuticals (Basel). 2010 May 14;3(5):1456-1490. doi: 10.3390/ph3051456.
9
Cell-Penetrating Peptides-Mechanisms of Cellular Uptake and Generation of Delivery Systems.细胞穿透肽——细胞摄取机制与递送系统的生成
Pharmaceuticals (Basel). 2010 Mar 30;3(4):961-993. doi: 10.3390/ph3040961.
10
Lipopolyplex for Therapeutic Gene Delivery and Its Application for the Treatment of Parkinson's Disease.用于治疗性基因递送的脂质多聚体及其在帕金森病治疗中的应用。
Front Aging Neurosci. 2016 Apr 5;8:68. doi: 10.3389/fnagi.2016.00068. eCollection 2016.