Elnaz Agi, Z. Mosaferi, Sepideh Khatamsaz, P. Cheraghi, Nooshin Samadian, A. Bolhassani
{"title":"Different strategies of gene delivery for treatment of cancer and other disorders","authors":"Elnaz Agi, Z. Mosaferi, Sepideh Khatamsaz, P. Cheraghi, Nooshin Samadian, A. Bolhassani","doi":"10.5430/JST.V6N2P76","DOIUrl":null,"url":null,"abstract":"Gene therapy is the gene transfer into host cells for treatment of acquired and genetic disorders. For this purpose, there are awide variety of gene delivery methods with special properties including viral and non-viral vectors. The non-viral methods usephysical forces or chemical compounds (natural or synthetic) to transfer DNA into a cell. The efficiency of the non-viral genetherapy depends on conquering four different intra- and extra-cellular barriers such as cellular uptake, endosomal escape, nuclearentry, and gene expression. Among various gene carriers, some viral vectors such as Adenovirus, Lentivirus, Vaccinia as well asgene gun and lipofection achieved to clinical trials. In this mini-review, we briefly describe different approaches for gene deliveryand their applications in various phases of clinical trials.","PeriodicalId":17174,"journal":{"name":"Journal of Solid Tumors","volume":"36 1","pages":"76"},"PeriodicalIF":0.0000,"publicationDate":"2016-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Solid Tumors","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5430/JST.V6N2P76","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
Gene therapy is the gene transfer into host cells for treatment of acquired and genetic disorders. For this purpose, there are awide variety of gene delivery methods with special properties including viral and non-viral vectors. The non-viral methods usephysical forces or chemical compounds (natural or synthetic) to transfer DNA into a cell. The efficiency of the non-viral genetherapy depends on conquering four different intra- and extra-cellular barriers such as cellular uptake, endosomal escape, nuclearentry, and gene expression. Among various gene carriers, some viral vectors such as Adenovirus, Lentivirus, Vaccinia as well asgene gun and lipofection achieved to clinical trials. In this mini-review, we briefly describe different approaches for gene deliveryand their applications in various phases of clinical trials.