Post-transcriptional gene-expression regulation by micro RNA (miRNA) network in renal disease
- PMID: 20940025
- DOI: 10.1016/j.addr.2010.10.003
Post-transcriptional gene-expression regulation by micro RNA (miRNA) network in renal disease
Abstract
Micro RNAs (miRNAs) are a recently discovered class of small, non-coding RNAs with the function of post-transcriptional gene expression regulation. MiRNAs may function in networks, forming a complex relationship with diseases. Alterations of specific miRNA levels have significant correlation with diseases of divergent origin, such as diabetic or ischemic organ injury including nephropathy, and malignant diseases including renal tumors. After identification of disease-associated miRNAs, there are two options of influencing their tissue expression. The function of miRNAs can be inhibited by antisense oligonucleotides (ASOs), which have been shown to silence specific miRNAs in vivo. Moreover, miRNA activity can be also mimicked or enhanced by delivering chemically synthesized miRNAs. Thus, modifying the expression of miRNAs is a potential future gene-therapeutic tool to influence posttranscriptional regulation of multiple genes in a single therapy. In this review we focus on key renal miRNAs with the aim of revealing the pathomechanisms of renal diseases. Nucleic acid therapy with oligonucleotides and short interfering RNA (siRNA) are under clinical evaluation presently. Similar therapeutic strategies, to influence miRNA function is also already under clinical investigation in RNA interference trials. We summarize here studies specifically aimed at the modification of miRNA expression. Research on the post-transcriptional regulation of gene expression by miRNA may reshape our understanding of renal pathophysiology and consequently may bring new diagnostic markers and therapeutic agents.
Copyright © 2010 Elsevier B.V. All rights reserved.
Similar articles
-
The huge world of small RNAs: regulating networks of microRNAs (review).Acta Physiol Hung. 2011 Sep;98(3):243-51. doi: 10.1556/APhysiol.98.2011.3.1. Acta Physiol Hung. 2011. PMID: 21893463 Review.
-
Review: The role of microRNAs in kidney disease.Nephrology (Carlton). 2010 Sep;15(6):599-608. doi: 10.1111/j.1440-1797.2010.01363.x. Nephrology (Carlton). 2010. PMID: 20883280 Review.
-
Current perspectives in intronic micro RNAs (miRNAs).J Biomed Sci. 2006 Jan;13(1):5-15. doi: 10.1007/s11373-005-9036-8. Epub 2005 Oct 14. J Biomed Sci. 2006. PMID: 16228283 Review.
-
Pharmacological potential of RNAi--focus on miRNA.Pharmacol Ther. 2010 Jun;126(3):217-27. doi: 10.1016/j.pharmthera.2010.03.006. Epub 2010 Apr 11. Pharmacol Ther. 2010. PMID: 20388525 Review.
-
Post-transcriptional gene silencing by siRNAs and miRNAs.Curr Opin Struct Biol. 2005 Jun;15(3):331-41. doi: 10.1016/j.sbi.2005.05.006. Curr Opin Struct Biol. 2005. PMID: 15925505 Review.
Cited by
-
The Mechanism and Function of Epigenetics in Uterine Leiomyoma Development.Reprod Sci. 2016 Feb;23(2):163-75. doi: 10.1177/1933719115584449. Epub 2015 Apr 28. Reprod Sci. 2016. PMID: 25922306 Free PMC article. Review.
-
Unveiling the potential of mitochondrial dynamics as a therapeutic strategy for acute kidney injury.Front Cell Dev Biol. 2023 Aug 11;11:1244313. doi: 10.3389/fcell.2023.1244313. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 37635869 Free PMC article. Review.
-
Metabolic reprogramming-based characterization of circulating tumor cells in prostate cancer.J Exp Clin Cancer Res. 2018 Jun 28;37(1):127. doi: 10.1186/s13046-018-0789-0. J Exp Clin Cancer Res. 2018. PMID: 29954422 Free PMC article.
-
Tight junctions and their regulation by non-coding RNAs.Int J Biol Sci. 2021 Jan 31;17(3):712-727. doi: 10.7150/ijbs.45885. eCollection 2021. Int J Biol Sci. 2021. PMID: 33767583 Free PMC article. Review.
-
Activation of the miR-17 family and miR-21 during murine kidney ischemia-reperfusion injury.Nucleic Acid Ther. 2013 Oct;23(5):344-54. doi: 10.1089/nat.2013.0438. Nucleic Acid Ther. 2013. PMID: 23988020 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical