RNA interference as a tool for Alzheimer's disease therapy

被引:37
作者
Orlacchio, Antonio
Bernardi, Giorgio
Orlacchi, Aldo
Martin, Sabata
机构
[1] IRCCS, Neurogenet Lab, CERC, I-00143 Rome, Italy
[2] Univ Roma Tor Vergata, Dipartimento Neurosci, Policlin tor Vergata Neurol, I-00133 Rome, Italy
[3] Univ Perugia, Sez Biochim & Biol Mol, Dipartimento Med Sperimentale & Sci Biochim, I-06126 Perugia, Italy
关键词
D O I
10.2174/138955707782331678
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
RNA interference is a biological process that controls gene silencing in all living cells. Targeting the RNA interference system represents a novel therapeutic strategy able to intercede with multiple disease-related genes and to target many neurodegenerative diseases. Recently, the design of small interfering RNA-selective compounds has become more straightforward because of the significant progress made in predictive modeling for new therapeutic approaches. Although in vivo delivery of RNA interference remains a significant obstacle, new data show that RNAi blocks gene function in vivo, suggesting a potential therapeutic approach for humans. Some groups have demonstrated the efficacy of RNAi therapy in Alzheimer's disease. Results, based on animal models, show a down-regulation of the amyloid precursor protein and a consequent reduction of the amyloid-beta peptide accumulation in the brain or the inactivation of beta-secretase (BACEI). Indeed, lentiviral vectors expressing siRNAs targeting BACEI reduce amyloid production and the neurodegencrative and behavioural deficit in APP transgenic mice. This review highlights recent advances in RNA research and focuses on strengths and weaknesses of RNAi compounds in Alzheimer's disease.
引用
收藏
页码:1166 / 1176
页数:11
相关论文
共 193 条
[31]   The intracellular domain of amyloid precursor protein interacts with flotillin-1, a lipid raft protein [J].
Chen, TY ;
Liu, PH ;
Ruan, CT ;
Chiu, L ;
Kung, FL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 342 (01) :266-272
[32]   Erythropoictin requires NF-κB and its nuclear translocation to prevent early and late apoptotic neuronal injury during β-amyloid toxicity [J].
Chong, ZZ ;
Li, FQ ;
Maiese, K .
CURRENT NEUROVASCULAR RESEARCH, 2005, 2 (05) :387-399
[33]   Intra- or intercomplex binding to the γ-secretase enzyme [J].
Clarke, Earl E. ;
Churcher, Ian ;
Ellis, Semantha ;
Wrigley, Jonathan D. J. ;
Lewis, Huw D. ;
Harrison, Timothy ;
Shearman, Mark S. ;
Beher, Dirk .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (42) :31279-31289
[34]   GSK3 inhibitors: Development and therapeutic potential [J].
Cohen, P ;
Goedert, M .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (06) :479-487
[35]   Structural domains in RNAi [J].
Collins, RE ;
Cheng, XD .
FEBS LETTERS, 2005, 579 (26) :5841-5849
[36]   Alzheimer disease-specific conformation of hyperphosphorylated paired helical filament-tau is polyubiquitinated through Lys-48, Lys-11, and Lys-6 ubiquitin conjugation [J].
Cripps, D ;
Thomas, SN ;
Jeng, Y ;
Yang, F ;
Davies, P ;
Yang, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (16) :10825-10838
[37]  
Cruts M, 1998, HUM MUTAT, V11, P183, DOI 10.1002/(SICI)1098-1004(1998)11:3<183::AID-HUMU1>3.3.CO
[38]  
2-M
[39]   Presenilins and Alzheimer's disease: biological functions and pathogenic mechanisms [J].
Czech, C ;
Tremp, G ;
Pradier, L .
PROGRESS IN NEUROBIOLOGY, 2000, 60 (04) :363-384
[40]   γ-secretase modulation with Aβ42-lowering nonsteroidal anti-inflammatory drugs and derived compounds [J].
Czirr, Eva ;
Weggen, Sascha .
NEURODEGENERATIVE DISEASES, 2006, 3 (4-5) :298-304