RNA therapeutics targeting osteoclast-mediated excessive bone resorption

被引:43
作者
Wang, Yuwei [1 ]
Grainger, David W. [1 ,2 ]
机构
[1] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
关键词
siRNA; Osteoclast; Molecular target; Bone resorption; Osteoporosis; Gene therapy; RNAi; NF-KAPPA-B; SMALL INTERFERING RNA; CALCIUM-PHOSPHATE CEMENT; TOTAL HIP-ARTHROPLASTY; DRUG-DELIVERY SYSTEM; INTERCELLULAR-ADHESION MOLECULE-1; FUNCTION-ASSOCIATED ANTIGEN-1; ACTIN RING FORMATION; DOUBLE-STRANDED-RNA; IN-VITRO;
D O I
10.1016/j.addr.2011.09.002
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
RNA interference (RNAi) is a sequence-specific post-transcriptional gene silencing technique developed with dramatically increasing utility for both scientific and therapeutic purposes. Short interfering RNA (siRNA) is currently exploited to regulate protein expression relevant to many therapeutic applications, and commonly used as a tool for elucidating disease-associated genes. Osteoporosis and their associated osteoporotic fragility fractures in both men and women are rapidly becoming a global healthcare crisis as average life expectancy increases worldwide. New therapeutics are needed for this increasing patient population. This review describes the diversity of molecular targets suitable for RNAi-based gene knock down in osteoclasts to control osteoclast-mediated excessive bone resorption. We identify strategies for developing targeted siRNA delivery and efficient gene silencing, and describe opportunities and challenges of introducing siRNA as a therapeutic approach to hard and connective tissue disorders. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1341 / 1357
页数:17
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