Literature DB >> 20940025

Post-transcriptional gene-expression regulation by micro RNA (miRNA) network in renal disease.

Tamás Kaucsár1, Zsuzsanna Rácz, Péter Hamar.   

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.

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Year:  2010        PMID: 20940025     DOI: 10.1016/j.addr.2010.10.003

Source DB:  PubMed          Journal:  Adv Drug Deliv Rev        ISSN: 0169-409X            Impact factor:   15.470


  17 in total

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2.  The Effect of Regular Moderate Exercise on miRNA-192 Expression Changes in Kidney of Streptozotocin-Induced Diabetic Male Rats.

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Review 3.  The Mechanism and Function of Epigenetics in Uterine Leiomyoma Development.

Authors:  Qiwei Yang; Aymara Mas; Michael P Diamond; Ayman Al-Hendy
Journal:  Reprod Sci       Date:  2015-04-28       Impact factor: 3.060

4.  Recent Advances in Understanding of NASH: MicroRNAs as Both Biochemical Markers and Players.

Authors:  Robert Vincent; Arun Sanyal
Journal:  Curr Pathobiol Rep       Date:  2014-09-01

5.  Urine miRNAs: potential biomarkers for monitoring progression of early stages of diabetic nephropathy.

Authors:  Yeyi Yang; Li Xiao; Jun Li; Yashpal S Kanwar; Fuyou Liu; Lin Sun
Journal:  Med Hypotheses       Date:  2013-05-14       Impact factor: 1.538

6.  Activation of the miR-17 family and miR-21 during murine kidney ischemia-reperfusion injury.

Authors:  Tamás Kaucsár; Csaba Révész; Mária Godó; Tibor Krenács; Mihály Albert; Csaba Imre Szalay; László Rosivall; Zoltán Benyó; Sándor Bátkai; Thomas Thum; Gábor Szénási; Péter Hamar
Journal:  Nucleic Acid Ther       Date:  2013-10       Impact factor: 5.486

7.  Bone marrow mesenchymal stem cells-induced exosomal microRNA-486-3p protects against diabetic retinopathy through TLR4/NF-κB axis repression.

Authors:  W Li; L Jin; Y Cui; A Nie; N Xie; G Liang
Journal:  J Endocrinol Invest       Date:  2020-09-26       Impact factor: 4.256

8.  MicroRNAs in HIV-associated nephropathy (HIVAN).

Authors:  Kang Cheng; Partab Rai; Andrei Plagov; Xiqian Lan; Ashaan Subrati; Mohammad Husain; Ashwani Malhotra; Pravin C Singhal
Journal:  Exp Mol Pathol       Date:  2012-10-16       Impact factor: 3.362

Review 9.  Role of regulatory micro RNAs in type 2 diabetes mellitus-related inflammation.

Authors:  Péter Hamar
Journal:  Nucleic Acid Ther       Date:  2012-09-05       Impact factor: 5.486

10.  Functional implications of microRNA-215 in TGF-β1-induced phenotypic transition of mesangial cells by targeting CTNNBIP1.

Authors:  Jiao Mu; Qi Pang; Yan-Hong Guo; Ji-Gang Chen; Wei Zeng; Yong-Jun Huang; Jun Zhang; Bing Feng
Journal:  PLoS One       Date:  2013-03-12       Impact factor: 3.240

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