Differential Expression of microRNAs in Serum of Patients with Chronic Painful Polyneuropathy and Healthy Age-Matched Controls

Polyneuropathies (PNP) are the most common type of disorder of the peripheral nervous system in adults. However, information on microRNA expression in PNP is lacking. Following microRNA sequencing, we compared the expression of microRNAs in the serum of patients experiencing chronic painful PNP with...

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Main Authors: Antonio Pellegrino, Sophie-Charlotte Fabig, Dilara Kersebaum, Philipp Hüllemann, Ralf Baron, Toralf Roch, Nina Babel, Harald Seitz
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/11/3/764
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author Antonio Pellegrino
Sophie-Charlotte Fabig
Dilara Kersebaum
Philipp Hüllemann
Ralf Baron
Toralf Roch
Nina Babel
Harald Seitz
author_facet Antonio Pellegrino
Sophie-Charlotte Fabig
Dilara Kersebaum
Philipp Hüllemann
Ralf Baron
Toralf Roch
Nina Babel
Harald Seitz
author_sort Antonio Pellegrino
collection DOAJ
description Polyneuropathies (PNP) are the most common type of disorder of the peripheral nervous system in adults. However, information on microRNA expression in PNP is lacking. Following microRNA sequencing, we compared the expression of microRNAs in the serum of patients experiencing chronic painful PNP with healthy age-matched controls. We have been able to identify four microRNAs (<i>hsa</i>-miR-3135b, <i>hsa</i>-miR-584-5p, <i>hsa</i>-miR-12136, and <i>hsa</i>-miR-550a-3p) that provide possible molecular links between degenerative processes, blood flow regulation, and signal transduction, that eventually lead to PNP. In addition, these microRNAs are discussed regarding the targeting of proteins that are involved in high blood flow/pressure and neural activity dysregulations/disbalances, presumably resulting in PNP-typical symptoms such as chronical numbness/pain. Within our study, we have identified four microRNAs that may serve as potential novel biomarkers of chronic painful PNP, and that may potentially bear therapeutic implications.
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spelling doaj.art-2d9e38fdd667439798f2a65b9be09eab2023-11-17T09:45:17ZengMDPI AGBiomedicines2227-90592023-03-0111376410.3390/biomedicines11030764Differential Expression of microRNAs in Serum of Patients with Chronic Painful Polyneuropathy and Healthy Age-Matched ControlsAntonio Pellegrino0Sophie-Charlotte Fabig1Dilara Kersebaum2Philipp Hüllemann3Ralf Baron4Toralf Roch5Nina Babel6Harald Seitz7Fraunhofer Institute for Cell Therapy and Immunology, Branch Bioanalytics and Bioprocesses (IZI-BB), 14476 Potsdam, GermanyDivision of Neurological Pain Research and Therapy, Department of Neurology, University Hospital Schleswig-Holstein, 24105 Kiel, GermanyDivision of Neurological Pain Research and Therapy, Department of Neurology, University Hospital Schleswig-Holstein, 24105 Kiel, GermanyDivision of Neurological Pain Research and Therapy, Department of Neurology, University Hospital Schleswig-Holstein, 24105 Kiel, GermanyDivision of Neurological Pain Research and Therapy, Department of Neurology, University Hospital Schleswig-Holstein, 24105 Kiel, GermanyBerlin Institute of Health at Charité—University Clinic Berlin, BIH Center for Regenerative Therapies, 13353 Berlin, GermanyBerlin Institute of Health at Charité—University Clinic Berlin, BIH Center for Regenerative Therapies, 13353 Berlin, GermanyFraunhofer Institute for Cell Therapy and Immunology, Branch Bioanalytics and Bioprocesses (IZI-BB), 14476 Potsdam, GermanyPolyneuropathies (PNP) are the most common type of disorder of the peripheral nervous system in adults. However, information on microRNA expression in PNP is lacking. Following microRNA sequencing, we compared the expression of microRNAs in the serum of patients experiencing chronic painful PNP with healthy age-matched controls. We have been able to identify four microRNAs (<i>hsa</i>-miR-3135b, <i>hsa</i>-miR-584-5p, <i>hsa</i>-miR-12136, and <i>hsa</i>-miR-550a-3p) that provide possible molecular links between degenerative processes, blood flow regulation, and signal transduction, that eventually lead to PNP. In addition, these microRNAs are discussed regarding the targeting of proteins that are involved in high blood flow/pressure and neural activity dysregulations/disbalances, presumably resulting in PNP-typical symptoms such as chronical numbness/pain. Within our study, we have identified four microRNAs that may serve as potential novel biomarkers of chronic painful PNP, and that may potentially bear therapeutic implications.https://www.mdpi.com/2227-9059/11/3/764differential expressionmicroRNAserumchronic painpolyneuropathy
spellingShingle Antonio Pellegrino
Sophie-Charlotte Fabig
Dilara Kersebaum
Philipp Hüllemann
Ralf Baron
Toralf Roch
Nina Babel
Harald Seitz
Differential Expression of microRNAs in Serum of Patients with Chronic Painful Polyneuropathy and Healthy Age-Matched Controls
Biomedicines
differential expression
microRNA
serum
chronic pain
polyneuropathy
title Differential Expression of microRNAs in Serum of Patients with Chronic Painful Polyneuropathy and Healthy Age-Matched Controls
title_full Differential Expression of microRNAs in Serum of Patients with Chronic Painful Polyneuropathy and Healthy Age-Matched Controls
title_fullStr Differential Expression of microRNAs in Serum of Patients with Chronic Painful Polyneuropathy and Healthy Age-Matched Controls
title_full_unstemmed Differential Expression of microRNAs in Serum of Patients with Chronic Painful Polyneuropathy and Healthy Age-Matched Controls
title_short Differential Expression of microRNAs in Serum of Patients with Chronic Painful Polyneuropathy and Healthy Age-Matched Controls
title_sort differential expression of micrornas in serum of patients with chronic painful polyneuropathy and healthy age matched controls
topic differential expression
microRNA
serum
chronic pain
polyneuropathy
url https://www.mdpi.com/2227-9059/11/3/764
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