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阳离子脂质介导的基因转移:当前概念

Cationic lipid-mediated gene transfer: current concepts.

作者信息

Clark P R, Hersh E M

机构信息

Arizona Cancer Center, University of Arizona, Tucson 85724, USA.

出版信息

Curr Opin Mol Ther. 1999 Apr;1(2):158-76.

Abstract

Infectious disease, heart disease, cancer, autoimmunity, genetic defects and even traumatic injury may someday be treated with gene therapy and gene transfer strategies. The potential impact of this new technology on human disease has produced optimism and expectation for scientists and lay people alike. As more effort is directed at harvesting the potential of this technology it has become clear that the success or failure of gene therapy will hinge on our ability to manipulate and control the process of gene transfer in somatic cells. Today, somatic gene transfer is accomplished using either viral or non-viral gene transfer methods. The benefits and limitations of each system are aggressively being investigated to determine which characteristics are most compatible with safe and reliable gene transfer. Gene transfer with cationic lipid/plasmid DNA complexes (cationic lipoplexes) has become a popular means of delivering therapeutic genes and is being tested in preclinical and clinical trials. Cationic lipoplexes are easy and inexpensive to produce, they are composed of non-toxic and non-immunogenic precursor, and they have the potential of delivering large polynucleotides into somatic cells. Additionally, these reagents are easily manipulated in the laboratory to incorporate novel biological functions or to produce new formulations that can be screened for in vivo gene transfer activity. The last few years has seen many advances in our understanding of molecular and biological factors that influence cationic lipid-mediated gene transfer. In this review we discuss recent developments in the field of cationic lipid-mediated gene transfer with emphasis on in vivo application where possible. We will consider new discoveries concerning the molecular and cellular events that control the uptake, transit and expression of lipoplexes in somatic cells. Recent biodistribution and pharmacokinetic studies and current concepts regarding the toxicity and immunogenicity of cationic lipoplexes will also be discussed. We also survey some of the many preclinical and clinical trials using cationic lipid-mediated gene transfer, with emphasis on cancer applications.

摘要

传染病、心脏病、癌症、自身免疫性疾病、基因缺陷甚至创伤性损伤,未来某天或许都可用基因治疗和基因转移策略来治疗。这项新技术对人类疾病的潜在影响,让科学家和普通大众都满怀乐观与期待。随着越来越多的努力致力于挖掘这项技术的潜力,基因治疗的成败显然将取决于我们操纵和控制体细胞中基因转移过程的能力。如今,体细胞基因转移是通过病毒或非病毒基因转移方法来实现的。人们正在积极研究每种系统的优缺点,以确定哪些特性最适合安全可靠的基因转移。阳离子脂质/质粒DNA复合物(阳离子脂质体)介导的基因转移已成为递送治疗性基因的常用手段,并正在进行临床前和临床试验。阳离子脂质体易于制备且成本低廉,由无毒且无免疫原性的前体组成,有潜力将大的多核苷酸递送至体细胞。此外,这些试剂在实验室中易于操作,可整合新的生物学功能或制备新的制剂,用于筛选体内基因转移活性。在过去几年里,我们对影响阳离子脂质介导的基因转移的分子和生物学因素的理解有了许多进展。在这篇综述中,我们将讨论阳离子脂质介导的基因转移领域的最新进展,并尽可能侧重于体内应用。我们将考虑有关控制脂质体在体细胞中摄取、转运和表达的分子和细胞事件的新发现。还将讨论最近的生物分布和药代动力学研究,以及关于阳离子脂质体毒性和免疫原性的当前概念。我们还将概述一些使用阳离子脂质介导的基因转移的临床前和临床试验,重点是癌症应用。

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