Micelleplexes as nucleic acid delivery systems for cancer-targeted therapies.
Cancer targeting
Gene delivery
Micelleplexes
Multidrug resistance
Nucleic acid therapeutics
Nucleic acids
Journal
Journal of controlled release : official journal of the Controlled Release Society
ISSN: 1873-4995
Titre abrégé: J Control Release
Pays: Netherlands
ID NLM: 8607908
Informations de publication
Date de publication:
10 07 2020
10 07 2020
Historique:
received:
24
01
2020
revised:
23
04
2020
accepted:
24
04
2020
pubmed:
1
5
2020
medline:
22
6
2021
entrez:
1
5
2020
Statut:
ppublish
Résumé
Cancer remains one of the leading causes of death worldwide despite significant therapeutic advancements and improved detection methods. Nucleic acid (NA) therapeutics are receiving increasing attention for cancer management and cure. Indeed, ribonucleic acid (RNA) oligonucleotides (such as small interfering RNA (siRNA) and micro RNA (miRNA)), messenger RNA (mRNA) and deoxyribonucleic acid (DNA) (such as plasmidic DNA (pDNA) and minicircle DNA (mcDNA)), have demonstrated potential as novel therapeutic agents. The imposing prospects of NA-based therapeutics reside in their ability to act as key-players mediating cellular pathways and bestowing potent gene silencing properties, as in the case of RNA interference (RNAi) agents, or by promoting the expression of specific required proteins for disease management (pDNA, mcDNA and mRNA, for instance). However, efficient NA therapeutics delivery is seriously hampered by NA physicochemical features, low in vivo serum stability and compromised cellular internalization, which swiftly reduce their biological activities. Recently, nano-based systems emerged as suitable vehicles for NA delivery. This review covers NA-carrying micelleplexes as robust and multifunctional polymer-based NA delivery systems, as well as the specific in vivo challenges for successful NA delivery to cancer cells and their prospects to become clinical reality, followed by a critical analysis of the major in vivo micelleplex-based cancer-targeted strategies accomplished till the present day.
Identifiants
pubmed: 32353488
pii: S0168-3659(20)30255-8
doi: 10.1016/j.jconrel.2020.04.041
pii:
doi:
Substances chimiques
Micelles
0
Nucleic Acids
0
Polymers
0
RNA, Small Interfering
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
442-462Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.