RNA-based therapy for osteogenesis.


Journal

International journal of pharmaceutics
ISSN: 1873-3476
Titre abrégé: Int J Pharm
Pays: Netherlands
ID NLM: 7804127

Informations de publication

Date de publication:
05 Oct 2019
Historique:
received: 30 04 2019
revised: 02 08 2019
accepted: 03 08 2019
pubmed: 9 8 2019
medline: 28 1 2020
entrez: 9 8 2019
Statut: ppublish

Résumé

Nucleic acid-based therapy has shown great promise in accelerating bone regeneration as well as other diseases. Nucleic acids used in gene therapy mainly are either plasmid DNA (pDNA) or RNAs. Although pDNA therapy has been extensively studied for decades with encouraging preclinical and clinical results, side effects, and low efficiency associated with nuclear trafficking are hard to bypass. Unlike pDNA, RNAs (mRNA, siRNA, miRNA) exert their function in the cytoplasm, thereby being more efficient in hard-to-transfect cells such as primary osteoblasts. RNA interference-based gene silencing represents a negative regulation which knockdown the expression of antagonists that impair osteogenesis process. In contrary, mRNA therapy for osteogenesis represents a positive regulation which delivers mRNA encoding growth factors to accelerate bone regeneration. This review presents a comprehensive summary of the mRNA and siRNA-based therapies and the targets for bone regeneration in case of bone defect and osteoporosis.

Identifiants

pubmed: 31394184
pii: S0378-5173(19)30639-8
doi: 10.1016/j.ijpharm.2019.118594
pii:
doi:

Substances chimiques

RNA, Messenger 0
RNA, Small Interfering 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

118594

Informations de copyright

Copyright © 2019. Published by Elsevier B.V.

Auteurs

Pinpin Wang (P)

Centre de Biophysique Moléculaire UPR4301 CNRS, Rue Charles Sadron, Orléans Cedex 02, France.

Federico Perche (F)

Centre de Biophysique Moléculaire UPR4301 CNRS, Rue Charles Sadron, Orléans Cedex 02, France.

Delphine Logeart-Avramoglou (D)

Laboratory of Osteoarticular Biology, Bioengineering and Bioimaging, UMR CNRS 7052 INSERM U1271, 10, Avenue de Verdun, 75010 Paris, France.

Chantal Pichon (C)

Centre de Biophysique Moléculaire UPR4301 CNRS, Rue Charles Sadron, Orléans Cedex 02, France. Electronic address: pichon@cnrs.fr.

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Classifications MeSH