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Bone site-specific delivery of siRNA

Small interfering RNAs (siRNA) have enormous potential as therapeutics to target and treat various bone disorders such as osteoporosis and cancer bone metastases. However, effective and specific delivery of siRNA therapeutics to bone and bone-specific cells in vivo is very challenging. To realize th...

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Detalles Bibliográficos
Autor principal: Liu, Xinli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Department of Journal of Biomedical Research 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946317/
https://www.ncbi.nlm.nih.gov/pubmed/26642236
http://dx.doi.org/10.7555/JBR.30.20150110
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author Liu, Xinli
author_facet Liu, Xinli
author_sort Liu, Xinli
collection PubMed
description Small interfering RNAs (siRNA) have enormous potential as therapeutics to target and treat various bone disorders such as osteoporosis and cancer bone metastases. However, effective and specific delivery of siRNA therapeutics to bone and bone-specific cells in vivo is very challenging. To realize the full therapeutic potential of siRNA in treating bone disorders, a safe and efficient, tissue- and cell-specific delivery system must be developed. This review focuses on recent advances in bone site-specific delivery of siRNA at the tissue or cellular level. Bone-targeted nanoparticulate siRNA carriers and various bone-targeted moieties such as bisphosphonates, oligopeptides (Asp)(8) and (AspSerSer)(6), and aptamers are highlighted. Incorporation of these bone-seeking targeting moieties into siRNA carriers allows for recognition of different sub-tissue functional domains of bone and also specific cell types residing in bone tissue. It also provides a means for bone-formation surface-, bone-resorption surface-, or osteoblast-specific targeting and transportation of siRNA therapeutics. The discussion mainly focuses on systemic and local bone-specific delivery of siRNA in osteoporosis and bone metastasis preclinical models.
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spelling pubmed-49463172016-07-25 Bone site-specific delivery of siRNA Liu, Xinli J Biomed Res Invited Review Small interfering RNAs (siRNA) have enormous potential as therapeutics to target and treat various bone disorders such as osteoporosis and cancer bone metastases. However, effective and specific delivery of siRNA therapeutics to bone and bone-specific cells in vivo is very challenging. To realize the full therapeutic potential of siRNA in treating bone disorders, a safe and efficient, tissue- and cell-specific delivery system must be developed. This review focuses on recent advances in bone site-specific delivery of siRNA at the tissue or cellular level. Bone-targeted nanoparticulate siRNA carriers and various bone-targeted moieties such as bisphosphonates, oligopeptides (Asp)(8) and (AspSerSer)(6), and aptamers are highlighted. Incorporation of these bone-seeking targeting moieties into siRNA carriers allows for recognition of different sub-tissue functional domains of bone and also specific cell types residing in bone tissue. It also provides a means for bone-formation surface-, bone-resorption surface-, or osteoblast-specific targeting and transportation of siRNA therapeutics. The discussion mainly focuses on systemic and local bone-specific delivery of siRNA in osteoporosis and bone metastasis preclinical models. Editorial Department of Journal of Biomedical Research 2016-07 2015-11-18 /pmc/articles/PMC4946317/ /pubmed/26642236 http://dx.doi.org/10.7555/JBR.30.20150110 Text en © 2016 by the Journal of Biomedical Research. All rights reserved.
spellingShingle Invited Review
Liu, Xinli
Bone site-specific delivery of siRNA
title Bone site-specific delivery of siRNA
title_full Bone site-specific delivery of siRNA
title_fullStr Bone site-specific delivery of siRNA
title_full_unstemmed Bone site-specific delivery of siRNA
title_short Bone site-specific delivery of siRNA
title_sort bone site-specific delivery of sirna
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946317/
https://www.ncbi.nlm.nih.gov/pubmed/26642236
http://dx.doi.org/10.7555/JBR.30.20150110
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