Literature DB >> 23035592

RNAi-based therapies for Huntington's disease: delivery challenges and opportunities.

Neelima Mantha1, Sudip K Das, Nandita G Das.   

Abstract

Huntington's disease (HD) is a polyglutamine neurodegenerative disease caused by a mutation in the HTT gene coding for the Huntingtin protein (HTT). Unfortunately, there is no cure for HD and there is also no known way to modify the disease progression. RNAi approaches offer the promise of a certain degree of control over the disease. However, there are several challenges in potential use of RNAi in the treatment of HD. This article will discuss the details of RNAi technology as applied to the treatment of HD, and novel approaches to overcome the drug delivery challenges.

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Year:  2012        PMID: 23035592     DOI: 10.4155/tde.12.80

Source DB:  PubMed          Journal:  Ther Deliv        ISSN: 2041-5990


  4 in total

Review 1.  Post-transcriptional gene silencing, transcriptional gene silencing and human immunodeficiency virus.

Authors:  Catalina Méndez; Chantelle L Ahlenstiel; Anthony D Kelleher
Journal:  World J Virol       Date:  2015-08-12

Review 2.  Rare-disease genetics in the era of next-generation sequencing: discovery to translation.

Authors:  Kym M Boycott; Megan R Vanstone; Dennis E Bulman; Alex E MacKenzie
Journal:  Nat Rev Genet       Date:  2013-09-03       Impact factor: 53.242

Review 3.  Transgenic animal models for study of the pathogenesis of Huntington's disease and therapy.

Authors:  Renbao Chang; Xudong Liu; Shihua Li; Xiao-Jiang Li
Journal:  Drug Des Devel Ther       Date:  2015-04-15       Impact factor: 4.162

4.  Efficient delivery of Notch1 siRNA to SKOV3 cells by cationic cholesterol derivative-based liposome.

Authors:  Yun-Chun Zhao; Li Zhang; Shi-Sen Feng; Lu Hong; Hai-Li Zheng; Li-Li Chen; Xiao-Ling Zheng; Yi-Qing Ye; Meng-Dan Zhao; Wen-Xi Wang; Cai-Hong Zheng
Journal:  Int J Nanomedicine       Date:  2016-10-20
  4 in total

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