Differentially expressed urinary exo-miRs and clinical outcomes in kidney recipients on short-term tacrolimus therapy: a pilot study

Author:

Costa de Freitas Renata Caroline1ORCID,Bortolin Raul Hernandes1ORCID,Vecchia Genvigir Fabiana Dalla1ORCID,Bonezi Vivian1ORCID,Crespo Hirata Thiago Dominguez1ORCID,Felipe Claudia Rosso2ORCID,Tedesco-Silva Helio2ORCID,Medina-Pestana José Osmar2ORCID,Cerda Alvaro3ORCID,Doi Sonia Quateli4,Hirata Mario Hiroyuki1ORCID,Crespo Hirata Rosario Dominguez1ORCID

Affiliation:

1. Department of Clinical & Toxicological Analyses, School of Pharmaceutical Sciences, University of Sao Paulo, Sao Paulo 05508-000, Brazil

2. Nephrology Division, Hospital do Rim, Federal University of Sao Paulo, Sao Paulo 04038-002, Brazil

3. Department of Basic Sciences, Center of Excellence in Translational Medicine, BIOREN, Universidad de La Frontera, Temuco 4810296, Chile

4. School of Medicine, Uniformed Services University, Bethesda, MD 20814, USA

Abstract

Aim: To analyze the expression of urinary exosome-derived miRNAs (exo-miRs) in kidney recipients on tacrolimus-based therapy. Patients & methods: Clinical and drug monitoring data were recorded from 23 kidney recipients. Expression of 93 exo-miRs was measured by quantitative PCR array and mRNA targets were explored. Results: 16 exo-miRs were differentially expressed, including marked upregulation of miR-155-5p, and downregulation of miR-223-3p and miR-1228-3p. Expression of miR-155-5p and miR-223-3p correlated with tacrolimus dose (p < 0.05), miR-223-3p with serum creatinine (p < 0.05), and miR-223-3p and miR-1228-3p with blood leukocytes (p < 0.05). 12 miRNAs have predicted targets involved in cell proliferation, apoptosis, stress response, PIK3/AKT/mTOR and TGF-β signaling pathways. Conclusion: Differentially expressed urinary exo-miRs may be useful markers to monitor tacrolimus therapy and graft function in kidney transplantation.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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