MicroRNAs and their delivery in diabetic fibrosis.


Journal

Advanced drug delivery reviews
ISSN: 1872-8294
Titre abrégé: Adv Drug Deliv Rev
Pays: Netherlands
ID NLM: 8710523

Informations de publication

Date de publication:
03 2022
Historique:
received: 19 03 2021
revised: 21 09 2021
accepted: 04 11 2021
pubmed: 13 11 2021
medline: 19 3 2022
entrez: 12 11 2021
Statut: ppublish

Résumé

The global prevalence of diabetes mellitus was estimated to be 463 million people in 2019 and is predicted to rise to 700 million by 2045. The associated financial and societal costs of this burgeoning epidemic demand an understanding of the pathology of this disease, and its complications, that will inform treatment to enable improved patient outcomes. Nearly two decades after the sequencing of the human genome, the significance of noncoding RNA expression is still being assessed. The family of functional noncoding RNAs known as microRNAs regulates the expression of most genes encoded by the human genome. Altered microRNA expression profiles have been observed both in diabetes and in diabetic complications. These transcripts therefore have significant potential and novelty as targets for therapy, therapeutic agents and biomarkers.

Identifiants

pubmed: 34767865
pii: S0169-409X(21)00438-5
doi: 10.1016/j.addr.2021.114045
pii:
doi:

Substances chimiques

Biomarkers 0
Drug Carriers 0
Hypoglycemic Agents 0
MicroRNAs 0
Nanoparticle Drug Delivery System 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

114045

Subventions

Organisme : Medical Research Council
ID : MR/K010492/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/T002263/1
Pays : United Kingdom
Organisme : Department of Health
ID : II-LA-0712-20003
Pays : United Kingdom

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: TB and DF are inventors for patent WO/2017/129977 Chronic Kidney Disease Diagnostic. LD is the recipient of PhD studentship co-funding from Regulus Therapeutics and GSK.

Auteurs

Alexa Wonnacott (A)

Wales Kidney Research Unit, Division of Infection & Immunity, School of Medicine, College of Biomedical and Life Sciences, Cardiff University, Heath Park, Cardiff CF14 4XN, UK.

Laura Denby (L)

Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, Little France Crescent, Edinburgh EH16 4TJ, UK.

Richard J M Coward (RJM)

Bristol Renal, Dorothy Hodgkin Building, Bristol Medical School, University of Bristol, Bristol BS1 3NY, UK.

Donald J Fraser (DJ)

Wales Kidney Research Unit, Division of Infection & Immunity, School of Medicine, College of Biomedical and Life Sciences, Cardiff University, Heath Park, Cardiff CF14 4XN, UK.

Timothy Bowen (T)

Wales Kidney Research Unit, Division of Infection & Immunity, School of Medicine, College of Biomedical and Life Sciences, Cardiff University, Heath Park, Cardiff CF14 4XN, UK. Electronic address: bowent@cardiff.ac.uk.

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