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Urinary Exosomal miRNA Signature in Type II Diabetic Nephropathy Patients.
Denis Delić1, Claudia Eisele1, Ramona Schmid1
1Translational Medicine & Clinical Pharmacology, Boehringer Ingelheim Pharma GmbH & Co. KG, Birkendorferstr.65, 88397 Biberach, Germany.
Plos One
|March 2, 2016
Summary
Urinary exosomal microRNAs (miRNAs) are altered in type II diabetic nephropathy (DN) patients. Deregulated miR-320c shows potential as a marker for DN progression, impacting the TGF-β pathway.
Area of Science:
- Biochemistry and Molecular Biology
- Nephrology
- Genetics
Background:
- MicroRNAs (miRNAs) are key post-transcriptional regulators implicated in diabetic nephropathy (DN) pathogenesis.
- Urinary exosomal miRNAs are stable and reflect renal status, making them promising biomarkers.
Purpose of the Study:
- To profile urinary exosomal miRNAs in healthy controls, type II diabetes (T2D) patients, and T2D with nephropathy (DN) patients.
- To identify specific miRNAs associated with DN and its progression.
Main Methods:
- Urinary exosomal miRNA profiling using Agilent's miRNA microarrays in 8 controls, 8 T2D, and 8 DN patients.
- Validation of key miRNA expression using qRT-PCR.
- Correlation analysis with micro-albuminuria levels.
Main Results:
- 16 miRNA species showed significant deregulation (>2-fold) in DN patients compared to controls and T2D patients.
- 14 miRNAs were upregulated, and 2 were downregulated in DN patients.
- Deregulation was observed in micro-albuminuric DN patients, with miR-320c and miR-6068 showing strong upregulation and correlation with micro-albuminuria.
Conclusions:
- Urinary exosomal miRNA profiles are altered in type II diabetic nephropathy.
- Deregulated miR-320c, potentially targeting the TGF-β pathway via TSP-1, is a promising candidate biomarker for monitoring DN progression.
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