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
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

442-462

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Miguel Pereira-Silva (M)

Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra, Univ. Coimbra, Portugal.

Ivana Jarak (I)

Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra, Univ. Coimbra, Portugal.

Carmen Alvarez-Lorenzo (C)

Departamento de Farmacología, Farmacia y Tecnología Farmacéutica, I+DFarma Group (GI-1645), Facultad de Farmacia and Health Research Institute of Santiago de Compostela (IDIS), Universidade de Santiago de Compostela, Spain.

Angel Concheiro (A)

Departamento de Farmacología, Farmacia y Tecnología Farmacéutica, I+DFarma Group (GI-1645), Facultad de Farmacia and Health Research Institute of Santiago de Compostela (IDIS), Universidade de Santiago de Compostela, Spain.

Ana Cláudia Santos (AC)

Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra, Univ. Coimbra, Portugal; REQUIMTE/LAQV, Group of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra, Univ. Coimbra, Portugal.

Francisco Veiga (F)

Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra, Univ. Coimbra, Portugal; REQUIMTE/LAQV, Group of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra, Univ. Coimbra, Portugal.

Ana Figueiras (A)

Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra, Univ. Coimbra, Portugal; REQUIMTE/LAQV, Group of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra, Univ. Coimbra, Portugal. Electronic address: rfigueiras@ff.uc.pt.

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Classifications MeSH