Literature DB >> 19394374

Conditional RNAi: towards a silent gene therapy.

Sang-Kyung Lee1, Priti Kumar.   

Abstract

RNA interference (RNAi) has the potential to permit the downregulation of virtually any gene. While transgenic RNAi enables stable propagation of the resulting phenotype to progeny, the dominant nature of RNAi limits its use to applications where the continued suppression of gene expression does not disturb normal cell functioning. This is of particular importance when the target gene product is essential for cell survival, development or differentiation. It is therefore desirable that knockdown be externally regulatable. This review is aimed at providing an overview of the approaches for conditional RNAi in mammalian systems, with a special mention of studies employing these approaches to target therapeutically/biologically relevant molecules, their advantages and disadvantages, and a pointer towards approaches best suited for RNAi-based gene therapy.

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Year:  2009        PMID: 19394374     DOI: 10.1016/j.addr.2009.03.016

Source DB:  PubMed          Journal:  Adv Drug Deliv Rev        ISSN: 0169-409X            Impact factor:   15.470


  15 in total

Review 1.  Conditional gene manipulation: Cre-ating a new biological era.

Authors:  Jian Zhang; Jing Zhao; Wen-jie Jiang; Xi-wei Shan; Xiao-mei Yang; Jian-gang Gao
Journal:  J Zhejiang Univ Sci B       Date:  2012-07       Impact factor: 3.066

Review 2.  In vivo RNAi: today and tomorrow.

Authors:  Norbert Perrimon; Jian-Quan Ni; Lizabeth Perkins
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-06-09       Impact factor: 10.005

3.  Sniffing for gene-silencing efficiency of siRNAs in HeLa cells in comparison with that in HEK293T cells: correlation between knockdown efficiency and sustainability of sirnas revealed by FRET-based probing.

Authors:  Seonmi Shin; Yea Seul Kim; Jisu Kim; Hyun-Mi Kwon; Dong-Eun Kim; Sang Soo Hah
Journal:  Nucleic Acid Ther       Date:  2013-02-13       Impact factor: 5.486

4.  Effect of adenovirus-mediated RNA interference of IL-1β expression on spinal cord injury in rats.

Authors:  W-P Lin; J-H Lin; B Cai; J-X Shi; W-J Li; G R Choudhury; S-Q Wu; J-Z Wu; H-P Wu; Q-F Ke
Journal:  Spinal Cord       Date:  2016-02-23       Impact factor: 2.772

5.  Targeted therapy via oral administration of attenuated Salmonella expression plasmid-vectored Stat3-shRNA cures orthotopically transplanted mouse HCC.

Authors:  Y Tian; B Guo; H Jia; K Ji; Y Sun; Y Li; T Zhao; L Gao; Y Meng; D V Kalvakolanu; D J Kopecko; X Zhao; L Zhang; D Xu
Journal:  Cancer Gene Ther       Date:  2012-05-04       Impact factor: 5.987

6.  Inhibition of ATIR by shRNA prevents collagen synthesis in hepatic stellate cells.

Authors:  Peihong Dong; Fujun Yu; Xufei Fan; Zhuo Lin; Yongping Chen; Ji Li
Journal:  Mol Cell Biochem       Date:  2010-08-12       Impact factor: 3.396

Review 7.  RNA interference for improving the outcome of islet transplantation.

Authors:  Feng Li; Ram I Mahato
Journal:  Adv Drug Deliv Rev       Date:  2010-12-13       Impact factor: 15.470

8.  Gene silencing of non-obese diabetic receptor family (NLRP3) protects against the sepsis-induced hyper-bile acidaemia in a rat model.

Authors:  Y Wu; J Ren; B Zhou; C Ding; J Chen; G Wang; G Gu; X Wu; S Liu; D Hu; J Li
Journal:  Clin Exp Immunol       Date:  2015-02       Impact factor: 4.330

Review 9.  Genomic screening with RNAi: results and challenges.

Authors:  Stephanie Mohr; Chris Bakal; Norbert Perrimon
Journal:  Annu Rev Biochem       Date:  2010       Impact factor: 23.643

10.  TARGETgene: a tool for identification of potential therapeutic targets in cancer.

Authors:  Chia-Chin Wu; David D'Argenio; Shahab Asgharzadeh; Timothy Triche
Journal:  PLoS One       Date:  2012-08-31       Impact factor: 3.240

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