microRNAs: key modulators of disease-modifying therapies in multiple sclerosis.
Naeim EhteshamMeysam MosallaeiMohammad Reza KarimzadehHossein MoradikazerouniMohammadreza SharifiPublished in: International reviews of immunology (2020)
There is a high level of heterogeneity in symptom manifestations and response to disease-modifying therapies (DMTs) in multiple sclerosis (MS), an immune-based neurodegenerative disease with ever-increasing prevalence in recent decades. Because of unknown aspects of the etiopathology of MS and mechanism of action of DMTs, the reason for this variability is undetermined, and much remains to be understood. Traditionally, physicians consider switching to other DMTs based on the exacerbation of symptoms and/or change in the results of magnetic resonance imaging and biochemical factors. Therefore, identifying biological treatment response markers that help us recognizing non-responders rapidly and subsequently choosing another DMTs is necessary. microRNAs (miRNAs) are micromanagers of gene expression which have been profiled in different samples of MS patients, highlighting their role in pathogenetic of MS. Recent studies have investigated expression profiling of miRNAs after treatment with DMTs to clarify possible DMTs-mediated mechanism and obtaining response to therapy biomarkers. In this review, we will discuss the modulation of miRNAs by DMTs in cells and pathways involved in MS.
Keyphrases
- multiple sclerosis
- mass spectrometry
- gene expression
- ms ms
- magnetic resonance imaging
- white matter
- end stage renal disease
- primary care
- chronic kidney disease
- chronic obstructive pulmonary disease
- induced apoptosis
- dna methylation
- small molecule
- computed tomography
- high resolution
- risk factors
- intensive care unit
- stem cells
- mesenchymal stem cells
- cell proliferation
- diffusion weighted imaging
- cell death
- single molecule
- extracorporeal membrane oxygenation
- oxidative stress
- patient reported
- patient reported outcomes
- cell therapy
- contrast enhanced