Nanocurcumin restores aberrant miRNA expression profile in multiple sclerosis, randomized, double-blind, placebo-controlled trial.
Sanam DolatiLeili Aghebati-MalekiMajid AhmadiFaroogh MarofiZohreh BabalooHormoz AyramlooZahra JafarisavariHamid OskoueiAmir AfkhamVahid YounesiMohammad NouriMehdi YousefiPublished in: Journal of cellular physiology (2018)
In the current study, we aimed to identify nanocurcumin effects on microRNAs (miRNAs) in the peripheral blood of patients with relapsing-remitting multiple sclerosis (RRMS). We intended to investigate the expression pattern of these miRNAs in experimental settings in vivo. The expression levels of the selected 27 miRNAs known to be involved in the regulation of immune responses were analyzed in 50 RRMS patients and 35 healthy controls. The miRNA expression profiles were investigated by quantitative PCR (qPCR) at baseline and after 6 months of nanocurcumin therapy. Our data revealed that the expression of a number of microRNAs including miR-16, miR-17-92, miR-27, miR-29b, miR-126, miR-128, miR-132, miR-155, miR-326, miR-550, miR-15a, miR-19b, miR-106b, miR-320a, miR-363, miR-31, miR-150, and miR-340 is regulated by nanocurcumin. The results of the current work indicate that nanocurcumin is able to restore the expression pattern of dysregulated miRNAs in MS patients. We discovered that some miRNAs are deregulated in untreated patients compared with healthy controls and nanocurcumin-treated patients. This is a new finding that might represent the potential contribution of these miRNAs to MS pathogenesis. Taken together, these data provide novel insights into miRNA-dependent regulation of the function of B and T cells in MS disease and enrich our understanding of the effects mediated by a therapeutic approach that targets B and T cells.
Keyphrases
- cell proliferation
- long non coding rna
- multiple sclerosis
- long noncoding rna
- poor prognosis
- end stage renal disease
- double blind
- newly diagnosed
- ejection fraction
- immune response
- peritoneal dialysis
- rheumatoid arthritis
- randomized controlled trial
- clinical trial
- peripheral blood
- placebo controlled
- binding protein
- high resolution
- toll like receptor
- white matter
- bone marrow
- artificial intelligence
- climate change
- atomic force microscopy