Therapeutic potential of RNA interference for neurological disorders

被引:70
作者
Sah, Dinah W. Y. [1 ]
机构
[1] Alnylam Pharmaceut Inc, Cambridge, MA 02142 USA
关键词
RNA interference; nervous system; drug development;
D O I
10.1016/j.lfs.2006.06.011
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
During the past decade, numerous molecular mediators of neurodegenerative diseases and neurological disorders have been identified and validated, yet few novel therapies have emerged and the unmet medical needs remain high. These molecular mediators belong to target classes such as ion channels, neurotransmitters and neurotransmitter receptors, cytokines, growth factors, enzymes and other proteins. In some cases, substantial pre-clinical validation exists, but the molecular target has not been readily druggable with small molecules, proteins or antibodies. RNA interference represents a therapeutic approach applicable to such non-druggable targets. Both non-viral and viral delivery strategies are being undertaken for in vivo silencing of molecular targets by RNA interference, which has resulted in robust efficacy in animal models of Alzheimer's disease, ALS, Huntington's disease, spinocerebellar ataxia, anxiety, depression, neuropathic pain, encephalitis and glioblastoma. These proof-of-concept data in animal models, together with the commencement of clinical trials using RNA interference for macular degeneration and respiratory syncytial virus infection, point to the potential of direct RNA interference for neurological disorders and neurodegenerative diseases. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1773 / 1780
页数:8
相关论文
共 52 条
[1]   Role for a bidentate ribonuclease in the initiation step of RNA interference [J].
Bernstein, E ;
Caudy, AA ;
Hammond, SM ;
Hannon, GJ .
NATURE, 2001, 409 (6818) :363-366
[2]   An ATF2-derived peptide sensitizes melanomas to apoptosis and inhibits their growth and metastasis [J].
Bhoumik, A ;
Huang, TG ;
Ivanov, V ;
Gangi, L ;
Qiao, RF ;
Woo, SLC ;
Chen, SH ;
Ronai, Z .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 110 (05) :643-650
[3]   Inhibition of respiratory viruses by nasally administered siRNA [J].
Bitko, V ;
Musiyenko, A ;
Shulyayeva, O ;
Barik, S .
NATURE MEDICINE, 2005, 11 (01) :50-55
[4]   The Argonaute family: tentacles that reach into RNAi, developmental control, stem cell maintenance, and tumorigenesis [J].
Carmell, MA ;
Xuan, ZY ;
Zhang, MQ ;
Hannon, GJ .
GENES & DEVELOPMENT, 2002, 16 (21) :2733-2742
[5]  
CHASE KO, 2005, BRAIN DELIVERY MODIF
[6]   Transcription and processing of human microRNA precursors [J].
Cullen, BR .
MOLECULAR CELL, 2004, 16 (06) :861-865
[7]   RNAi the natural way [J].
Cullen, BR .
NATURE GENETICS, 2005, 37 (11) :1163-1165
[8]   Highly efficient small interfering RNA delivery to primary mammalian neurons induces MicroRNA-like effects before mRNA degradation [J].
Davidson, TJ ;
Harel, S ;
Arboleda, VA ;
Prunell, GF ;
Shelanski, ML ;
Greene, LA ;
Troy, CM .
JOURNAL OF NEUROSCIENCE, 2004, 24 (45) :10040-10046
[9]   siRNA relieves chronic neuropathic pain [J].
Dorn, G ;
Patel, S ;
Wotherspoon, G ;
Hemmings-Mieszczak, M ;
Barclay, J ;
Natt, FJC ;
Martin, P ;
Bevan, S ;
Fox, A ;
Ganju, P ;
Wishart, W ;
Hall, J .
NUCLEIC ACIDS RESEARCH, 2004, 32 (05) :e49
[10]   RNA interference is mediated by 21-and 22-nucleotide RNAs [J].
Elbashir, SM ;
Lendeckel, W ;
Tuschl, T .
GENES & DEVELOPMENT, 2001, 15 (02) :188-200