MicroRNAs in kidney injury and disease.


Journal

Nature reviews. Nephrology
ISSN: 1759-507X
Titre abrégé: Nat Rev Nephrol
Pays: England
ID NLM: 101500081

Informations de publication

Date de publication:
10 2022
Historique:
accepted: 11 07 2022
pubmed: 17 8 2022
medline: 23 9 2022
entrez: 16 8 2022
Statut: ppublish

Résumé

MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression by degrading or repressing the translation of their target messenger RNAs. As miRNAs are critical regulators of cellular homeostasis, their dysregulation is a crucial component of cell and organ injury. A substantial body of evidence indicates that miRNAs are involved in the pathophysiology of acute kidney injury (AKI), chronic kidney disease and allograft damage. Different subsets of miRNAs are dysregulated during AKI, chronic kidney disease and allograft rejection, which could reflect differences in the physiopathology of these conditions. miRNAs that have been investigated in AKI include miR-21, which has an anti-apoptotic role, and miR-214 and miR-668, which regulate mitochondrial dynamics. Various miRNAs are downregulated in diabetic kidney disease, including the miR-30 family and miR-146a, which protect against inflammation and fibrosis. Other miRNAs such as miR-193 and miR-92a induce podocyte dedifferentiation in glomerulonephritis. In transplantation, miRNAs have been implicated in allograft rejection and injury. Further work is needed to identify and validate miRNAs as biomarkers of graft function and of kidney disease development and progression. Use of combinations of miRNAs together with other molecular markers could potentially improve diagnostic or predictive power and facilitate clinical translation. In addition, targeting specific miRNAs at different stages of disease could be a promising therapeutic strategy.

Identifiants

pubmed: 35974169
doi: 10.1038/s41581-022-00608-6
pii: 10.1038/s41581-022-00608-6
doi:

Substances chimiques

Biomarkers 0
MIRN214 microRNA, human 0
MicroRNAs 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

643-662

Informations de copyright

© 2022. Springer Nature Limited.

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Auteurs

Nassim Mahtal (N)

Paris Cardiovascular Research Center - PARCC, Inserm, Université Paris Cité, Paris, France.

Olivia Lenoir (O)

Paris Cardiovascular Research Center - PARCC, Inserm, Université Paris Cité, Paris, France. olivia.lenoir@inserm.fr.

Claire Tinel (C)

Service de Néphrologie et Transplantation Adulte, Hôpital Necker-Enfants Malades, Université Paris Cité, Assistance Publique-Hôpitaux de Paris, Paris, France.
Institut Necker-Enfants Malades, Inserm, Université Paris Cité, Paris, France.

Dany Anglicheau (D)

Service de Néphrologie et Transplantation Adulte, Hôpital Necker-Enfants Malades, Université Paris Cité, Assistance Publique-Hôpitaux de Paris, Paris, France.
Institut Necker-Enfants Malades, Inserm, Université Paris Cité, Paris, France.

Pierre-Louis Tharaux (PL)

Paris Cardiovascular Research Center - PARCC, Inserm, Université Paris Cité, Paris, France. pierre-louis.tharaux@inserm.fr.

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