• 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

Gene therapy. Therapeutic approaches and implications.

作者信息

Mhashilkar A, Chada S, Roth J A, Ramesh R

机构信息

Introgen Therapeutics, Inc., Houston, TX 77030, USA.

出版信息

Biotechnol Adv. 2001 Jul;19(4):279-97. doi: 10.1016/s0734-9750(01)00063-5.

DOI:10.1016/s0734-9750(01)00063-5
PMID:14538077
Abstract

The present article is an overview of gene therapy with an emphasis on different approaches and its implications in the clinic. Genetic interventions have been applied to the diagnosis of and therapy for an array of human diseases. The initial concept of gene therapy was focused on the treatment of genetic diseases. Subsequently, the field of gene therapy has been expanded, with a major focus on cancer. Although the results of early gene therapy-based clinical trials have been encouraging, there is a need for gene delivery vectors that feature reduced immunogenicity and improved targeting ability. The results of phases I/II clinical trials have suggested the important role of gene therapy as a versatile and powerful treatment tool, especially for human cancers. One reasonable expectation is that performing gene therapy at an earlier stage in the disease process or for minimal residual disease may be more advantageous.

摘要

相似文献

1
Gene therapy. Therapeutic approaches and implications.
Biotechnol Adv. 2001 Jul;19(4):279-97. doi: 10.1016/s0734-9750(01)00063-5.
2
Monoclonal antibodies and therapy of human cancers.单克隆抗体与人类癌症的治疗
Biotechnol Adv. 2000 Aug;18(5):385-401. doi: 10.1016/s0734-9750(00)00043-4.
3
INGN 201: Ad-p53, Ad5CMV-p53, adenoviral p53, p53 gene therapy--introgen, RPR/INGN 201.INGN 201:腺病毒载体p53、Ad5CMV-p53、腺病毒p53、p53基因疗法——英特洛根公司,RPR/INGN 201。
Drugs R D. 2007;8(3):176-87. doi: 10.2165/00126839-200708030-00005.
4
Current Methods in Cardiac Gene Therapy: Overview.心脏基因治疗的当前方法:概述
Methods Mol Biol. 2017;1521:3-14. doi: 10.1007/978-1-4939-6588-5_1.
5
The future of human gene therapy.人类基因治疗的未来。
Mol Aspects Med. 2001 Jun;22(3):113-42. doi: 10.1016/s0098-2997(01)00004-8.
6
Gene therapy for cardiovascular disease: advances in vector development, targeting, and delivery for clinical translation.心血管疾病的基因治疗:载体开发、靶向及临床转化递送方面的进展
Cardiovasc Res. 2015 Oct 1;108(1):4-20. doi: 10.1093/cvr/cvv205. Epub 2015 Aug 3.
7
Clinical gene therapy - first international conference. 24-26 January 2002, Groningen, the Netherlands.临床基因治疗——首届国际会议。2002年1月24日至26日,荷兰格罗宁根
IDrugs. 2002 Mar;5(3):209-12.
8
Lentiviral vectors: a versatile tool to fight cancer.慢病毒载体:对抗癌症的多面手。
Curr Mol Med. 2013 May;13(4):602-25. doi: 10.2174/1566524011313040011.
9
Gene therapy for colon cancer.结肠癌的基因治疗。
Hematol Oncol Clin North Am. 1998 Jun;12(3):595-615. doi: 10.1016/s0889-8588(05)70010-1.
10
Viral-mediated gene transfer for cancer treatment.用于癌症治疗的病毒介导基因转移。
Curr Pharm Biotechnol. 2002 Jun;3(2):151-64. doi: 10.2174/1389201023378445.

引用本文的文献

1
A review of the tortuous path of nonviral gene delivery and recent progress.非病毒基因递送的曲折道路及近期进展述评。
Int J Biol Macromol. 2021 Jul 31;183:2055-2073. doi: 10.1016/j.ijbiomac.2021.05.192. Epub 2021 Jun 1.
2
The effect of polar headgroups and spacer length on the DNA transfection of cholesterol-based cationic lipids.极性头部基团和间隔长度对基于胆固醇的阳离子脂质体DNA转染的影响。
RSC Med Chem. 2020 Jan 6;11(2):212-224. doi: 10.1039/c9md00459a. eCollection 2020 Feb 1.
3
Nonionic surfactant vesicles composed of novel spermine-derivative cationic lipids as an effective gene carrier in vitro.
由新型精胺衍生物阳离子脂质组成的非离子表面活性剂囊泡作为一种有效的体外基因载体。
AAPS PharmSciTech. 2014 Jun;15(3):722-30. doi: 10.1208/s12249-014-0095-x. Epub 2014 Mar 13.
4
Structure relationship of cationic lipids on gene transfection mediated by cationic liposomes.阳离子脂质体介导基因转染中阳离子脂质的结构关系。
AAPS PharmSciTech. 2012 Dec;13(4):1302-8. doi: 10.1208/s12249-012-9857-5. Epub 2012 Sep 25.
5
Tumor suppressor gene-based nanotherapy: from test tube to the clinic.基于肿瘤抑制基因的纳米疗法:从试管到临床
J Drug Deliv. 2011;2011:465845. doi: 10.1155/2011/465845. Epub 2011 Jan 24.
6
Delivering the goods: viral and non-viral gene therapy systems and the inherent limits on cargo DNA and internal sequences.实现目标:病毒和非病毒基因治疗系统以及对载体DNA和内部序列的固有限制
Genetica. 2010 May;138(5):485-98. doi: 10.1007/s10709-009-9434-3. Epub 2010 Jan 19.
7
Gene therapy vectors: the prospects and potentials of the cut-and-paste transposons.基因治疗载体:剪切粘贴转座子的前景与潜力
Genetica. 2010 May;138(5):473-84. doi: 10.1007/s10709-009-9391-x. Epub 2009 Aug 2.
8
Preparation and characteristics of DNA-nanoparticles targeting to hepatocarcinoma cells.靶向肝癌细胞的DNA纳米颗粒的制备及其特性
World J Gastroenterol. 2004 Mar 1;10(5):660-3. doi: 10.3748/wjg.v10.i5.660.